Tubulin and Microtubule Metrics Infographic
Microtubule and tubulin metrics[1]

Microtubules are polymers of tubulin that form part of the cytoskeleton and provide structure and shape to eukaryotic cells. Microtubules can be as long as 50 micrometres, as wide as 23 to 27 nm[2] and have an inner diameter between 11 and 15 nm.[3] They are formed by the polymerization of a dimer of two globular proteins, alpha and beta tubulin into protofilaments that can then associate laterally to form a hollow tube, the microtubule.[4] The most common form of a microtubule consists of 13 protofilaments in the tubular arrangement.

Microtubules are one of the cytoskeletal filament systems in eukaryotic cells. The microtubule cytoskeleton is involved in the transport of material within cells, carried out by motor proteins that move on the surface of the microtubule.

Microtubules play an important role in a number of cellular processes. They are involved in maintaining the structure of the cell and, together with microfilaments and intermediate filaments, they form the cytoskeleton. They also make up the internal structure of cilia and flagella. They provide platforms for intracellular transport and are involved in a variety of cellular processes, including the movement of secretory vesicles, organelles, and intracellular macromolecular assemblies.[5] They are also involved in cell division (by mitosis and meiosis) and are the main constituents of mitotic spindles, which are used to pull eukaryotic chromosomes apart.

Microtubules are nucleated and organized by microtubule-organizing centres, such as the centrosome found in the center of many animal cells or the basal bodies of cilia and flagella, or the spindle pole bodies found in most fungi.

There are many proteins that bind to microtubules, including the motor proteins dynein and kinesin, microtubule-severing proteins like katanin, and other proteins important for regulating microtubule dynamics.[6] Recently an actin-like protein has been found in the gram-positive bacterium Bacillus thuringiensis, which forms a microtubule-like structure called a nanotubule, involved in plasmid segregation.[7] Other bacterial microtubules have a ring of five protofilaments.

History

Tubulin and microtubule-mediated processes, like cell locomotion, were seen by early microscopists, like Leeuwenhoek (1677). However, the fibrous nature of flagella and other structures were discovered two centuries later, with improved light microscopes, and confirmed in the 20th century with the electron microscope and biochemical studies.[8]

In vitro assays for microtubule motor proteins such as dynein and kinesin are researched by fluorescently tagging a microtubule and fixing either the microtubule or motor proteins to a microscope slide, then visualizing the slide with video-enhanced microscopy to record the travel of the motor proteins. This allows the movement of the motor proteins along the microtubule or the microtubule moving across the motor proteins.[9] Consequently, some microtubule processes can be determined by kymograph.[10]

Structure

Cartoon representation of the structure of α(yellow)/β(red)-tubulin heterodimer, GTP and GDP.[11]

In eukaryotes, microtubules are long, hollow cylinders made up of polymerized α- and β-tubulin dimers.[12] The inner space of the hollow microtubule cylinders is referred to as the lumen. The α and β-tubulin subunits are ~50% identical at the amino acid level, and both have a molecular weight of approximately 50 kDa.[13][14]

These α/β-tubulin dimers polymerize end-to-end into linear protofilaments that associate laterally to form a single microtubule, which can then be extended by the addition of more α/β-tubulin dimers. Typically, microtubules are formed by the parallel association of thirteen protofilaments, although microtubules composed of fewer or more protofilaments have been observed in various species [15] as well as in vitro.[16]

Microtubules have a distinct polarity that is critical for their biological function. Tubulin polymerizes end to end, with the β-subunits of one tubulin dimer contacting the α-subunits of the next dimer. Therefore, in a protofilament, one end will have the α-subunits exposed while the other end will have the β-subunits exposed. These ends are designated the (−) and (+) ends, respectively. The protofilaments bundle parallel to one another with the same polarity, so, in a microtubule, there is one end, the (+) end, with only β-subunits exposed, while the other end, the (−) end, has only α-subunits exposed. While microtubule elongation can occur at both the (+) and (−) ends, it is significantly more rapid at the (+) end.[17]

The lateral association of the protofilaments generates a pseudo-helical structure, with one turn of the helix containing 13 tubulin dimers, each from a different protofilament. In the most common "13-3" architecture, the 13th tubulin dimer interacts with the next tubulin dimer with a vertical offset of 3 tubulin monomers due to the helicity of the turn. There are other alternative architectures, such as 11-3, 12-3, 14-3, 15-4, or 16-4, that have been detected at a much lower occurrence.[18] Microtubules can also morph into other forms such as helical filaments, which are observed in protist organisms like foraminifera.[19] There are two distinct types of interactions that can occur between the subunits of lateral protofilaments within the microtubule called the A-type and B-type lattices. In the A-type lattice, the lateral associations of protofilaments occur between adjacent α and β-tubulin subunits (i.e. an α-tubulin subunit from one protofilament interacts with a β-tubulin subunit from an adjacent protofilament). In the B-type lattice, the α and β-tubulin subunits from one protofilament interact with the α and β-tubulin subunits from an adjacent protofilament, respectively. Experimental studies have shown that the B-type lattice is the primary arrangement within microtubules. However, in most microtubules there is a seam in which tubulin subunits interact α-β.[20]

The sequence and exact composition of molecules during microtubule formation can thus be summarised as follows: A β-tubulin connects in the context of a non-existent covalent bond with an α-tubulin, which in connected form are a heterodimer, since they consist of two different polypeptides (β-tubulin and α-tubulin). So after the heterodimers are formed, they join together to form long chains that rise figuratively in one direction (e.g. upwards). These heterodimers, which are connected in a certain direction, form protofilaments. These long chains (protofilaments) now gradually accumulate next to each other so that a tube-like structure is formed, which has a lumen typical of a tube. Accordingly, mostly 13 protofilaments form the outer wall of the microtubules. The heterodimers consist of a positive and negative end, with alpha-tubulin forming the negative end and beta-tubulin the positive end. Due to the fact that the heterodimers are stacked on top of each other, there is always a negative and positive end. Microtubules grow by an addition of heterodimers at the plus end.

Some species of Prosthecobacter also contain microtubules. The structure of these bacterial microtubules is similar to that of eukaryotic microtubules, consisting of a hollow tube of protofilaments assembled from heterodimers of bacterial tubulin A (BtubA) and bacterial tubulin B (BtubB). Both BtubA and BtubB share features of both α- and β-tubulin. Unlike eukaryotic microtubules, bacterial microtubules do not require chaperones to fold.[21] In contrast to the 13 protofilaments of eukaryotic microtubules, bacterial microtubules comprise only five.[22]

Intracellular organization

Microtubules are part of the cytoskeleton, a structural network within the cell's cytoplasm. The roles of the microtubule cytoskeleton include mechanical support, organization of the cytoplasm, transport, motility and chromosome segregation. In developing neurons microtubules are known as neurotubules,[23] and they can modulate the dynamics of actin, another component of the cytoskeleton.[24] A microtubule is capable of growing and shrinking in order to generate force, and there are motor proteins that allow organelles and other cellular components to be carried along a microtubule. This combination of roles makes microtubules important for organizing and moving intracellular constituents.

The organization of microtubules in the cell is cell-type specific. In epithelia, the minus-ends of the microtubule polymer are anchored near the site of cell-cell contact and organized along the apical-basal axis. After nucleation, the minus-ends are released and then re-anchored in the periphery by factors such as ninein and PLEKHA7.[25] In this manner, they can facilitate the transport of proteins, vesicles and organelles along the apical-basal axis of the cell. In fibroblasts and other mesenchymal cell-types, microtubules are anchored at the centrosome and radiate with their plus-ends outwards towards the cell periphery (as shown in the first figure). In these cells, the microtubules play important roles in cell migration. Moreover, the polarity of microtubules is acted upon by motor proteins, which organize many components of the cell, including the endoplasmic reticulum and the Golgi apparatus.

Components of the eukaryotic cytoskeleton. Actin filaments are shown in red, microtubules are in green, and the nuclei are in blue. The cytoskeleton provides the cell with an inner framework and enables it to move and change shape.

Microtubule polymerization

Nucleation

Nucleation is the event that initiates the formation of microtubules from the tubulin dimer. Microtubules are typically nucleated and organized by organelles called microtubule-organizing centers (MTOCs). Contained within the MTOC is another type of tubulin, γ-tubulin, which is distinct from the α- and β-subunits of the microtubules themselves. The γ-tubulin combines with several other associated proteins to form a lock washer-like structure known as the "γ-tubulin ring complex" (γ-TuRC). This complex acts as a template for α/β-tubulin dimers to begin polymerization; it acts as a cap of the (−) end while microtubule growth continues away from the MTOC in the (+) direction.[26]

The centrosome is the primary MTOC of most cell types. However, microtubules can be nucleated from other sites as well. For example, cilia and flagella have MTOCs at their base termed basal bodies. In addition, work from the Kaverina group at Vanderbilt, as well as others, suggests that the Golgi apparatus can serve as an important platform for the nucleation of microtubules.[27] Because nucleation from the centrosome is inherently symmetrical, Golgi-associated microtubule nucleation may allow the cell to establish asymmetry in the microtubule network. In recent studies, the Vale group at UCSF identified the protein complex augmin as a critical factor for centrosome-dependent, spindle-based microtubule generation. It that has been shown to interact with γ-TuRC and increase microtubule density around the mitotic spindle origin.[28]

Some cell types, such as plant cells, do not contain well defined MTOCs. In these cells, microtubules are nucleated from discrete sites in the cytoplasm. Other cell types, such as trypanosomatid parasites, have a MTOC but it is permanently found at the base of a flagellum. Here, nucleation of microtubules for structural roles and for generation of the mitotic spindle is not from a canonical centriole-like MTOC.

Polymerization

Following the initial nucleation event, tubulin monomers must be added to the growing polymer. The process of adding or removing monomers depends on the concentration of αβ-tubulin dimers in solution in relation to the critical concentration, which is the steady state concentration of dimers at which there is no longer any net assembly or disassembly at the end of the microtubule. If the dimer concentration is greater than the critical concentration, the microtubule will polymerize and grow. If the concentration is less than the critical concentration, the length of the microtubule will decrease.[29]

Microtubule dynamics

Dynamic instability

Dynamic instability refers to the coexistence of assembly and disassembly at the ends of a microtubule. The microtubule can dynamically switch between growing and shrinking phases in this region.[30] Tubulin dimers can bind two molecules of GTP, one of which can be hydrolyzed subsequent to assembly. During polymerization, the tubulin dimers are in the GTP-bound state.[12] The GTP bound to α-tubulin is stable and it plays a structural function in this bound state. However, the GTP bound to β-tubulin may be hydrolyzed to GDP shortly after assembly. The assembly properties of GDP-tubulin are different from those of GTP-tubulin, as GDP-tubulin is more prone to depolymerization.[31] A GDP-bound tubulin subunit at the tip of a microtubule will tend to fall off, although a GDP-bound tubulin in the middle of a microtubule cannot spontaneously pop out of the polymer. Since tubulin adds onto the end of the microtubule in the GTP-bound state, a cap of GTP-bound tubulin is proposed to exist at the tip of the microtubule, protecting it from disassembly. When hydrolysis catches up to the tip of the microtubule, it begins a rapid depolymerization and shrinkage. This switch from growth to shrinking is called a catastrophe. GTP-bound tubulin can begin adding to the tip of the microtubule again, providing a new cap and protecting the microtubule from shrinking. This is referred to as "rescue".[32]

"Search and capture" model

In 1986, Marc Kirschner and Tim Mitchison proposed that microtubules use their dynamic properties of growth and shrinkage at their plus ends to probe the three dimensional space of the cell. Plus ends that encounter kinetochores or sites of polarity become captured and no longer display growth or shrinkage. In contrast to normal dynamic microtubules, which have a half-life of 5–10 minutes, the captured microtubules can last for hours. This idea is commonly known as the "search and capture" model.[33] Indeed, work since then has largely validated this idea. At the kinetochore, a variety of complexes have been shown to capture microtubule (+)-ends.[34] Moreover, a (+)-end capping activity for interphase microtubules has also been described.[35] This later activity is mediated by formins,[36] the adenomatous polyposis coli protein, and EB1,[37] a protein that tracks along the growing plus ends of microtubules.

Regulation of microtubule dynamics

Post-translational modifications

Image of a fibroblast cell containing fluorescently labeled actin (red) and microtubules (green).

Although most microtubules have a half-life of 5–10 minutes, certain microtubules can remain stable for hours.[35] These stabilized microtubules accumulate post-translational modifications on their tubulin subunits by the action of microtubule-bound enzymes.[38][39] However, once the microtubule depolymerizes, most of these modifications are rapidly reversed by soluble enzymes. Since most modification reactions are slow while their reverse reactions are rapid, modified tubulin is only detected on long-lived stable microtubules. Most of these modifications occur on the C-terminal region of alpha-tubulin. This region, which is rich in negatively charged glutamate, forms relatively unstructured tails that project out from the microtubule and form contacts with motors. Thus, it is believed that tubulin modifications regulate the interaction of motors with the microtubule. Since these stable modified microtubules are typically oriented towards the site of cell polarity in interphase cells, this subset of modified microtubules provide a specialized route that helps deliver vesicles to these polarized zones. These modifications include:

  • Detyrosination: the removal of the C-terminal tyrosine from alpha-tubulin. This reaction exposes a glutamate at the new C-terminus. As a result, microtubules that accumulate this modification are often referred to as Glu-microtubules. Although the tubulin carboxypeptidase has yet to be identified, the tubulin—tyrosine ligase (TTL) is known.[40]
  • Delta2: the removal of the last two residues from the C-terminus of alpha-tubulin.[41] Unlike detyrosination, this reaction is thought to be irreversible and has only been documented in neurons.
  • Acetylation: the addition of an acetyl group to lysine 40 of alpha-tubulin. This modification occurs on a lysine that is accessible only from the inside of the microtubule, and it remains unclear how enzymes access the lysine residue. The nature of the tubulin acetyltransferase remains controversial, but it has been found that in mammals the major acetyltransferase is ATAT1.[42] however, the reverse reaction is known to be catalyzed by HDAC6.[43] The real impact of acetylation in the structure and function of microtubules remains elusive.[44]
  • Polyglutamylation: the addition of a glutamate polymer (typically 4-6 residues long[45]) to the gamma-carboxyl group of any one of five glutamates found near the end of alpha-tubulin. Enzymes related to TTL add the initial branching glutamate (TTL4,5 and 7), while other enzymes that belong to the same family lengthen the polyglutamate chain (TTL6,11 and 13).[39]
  • Polyglycylation: the addition of a glycine polymer (2-10 residues long) to the gamma-carboxyl group of any one of five glutamates found near the end of beta-tubulin. TTL3 and 8 add the initial branching glycine, while TTL10 lengthens the polyglycine chain.[39]

Tubulin is also known to be phosphorylated, ubiquitinated, sumoylated, and palmitoylated.[38]

Tubulin-binding drugs and chemical effects

A wide variety of drugs are able to bind to tubulin and modify its assembly properties. These drugs can have an effect at intracellular concentrations much lower than that of tubulin. This interference with microtubule dynamics can have the effect of stopping a cell's cell cycle and can lead to programmed cell death or apoptosis. However, there are data to suggest that interference of microtubule dynamics is insufficient to block the cells undergoing mitosis.[46] These studies have demonstrated that suppression of dynamics occurs at concentrations lower than those needed to block mitosis. Suppression of microtubule dynamics by tubulin mutations or by drug treatment have been shown to inhibit cell migration.[47] Both microtubule stabilizers and destabilizers can suppress microtubule dynamics.

The drugs that can alter microtubule dynamics include:

  • The cancer-fighting taxane class of drugs (paclitaxel (taxol) and docetaxel) block dynamic instability by stabilizing GDP-bound tubulin in the microtubule. Thus, even when hydrolysis of GTP reaches the tip of the microtubule, there is no depolymerization and the microtubule does not shrink back.

Taxanes (alone or in combination with platinum derivatives (carboplatine) or gemcitabine) are used against breast and gynecological malignancies, squamous-cell carcinomas (head-and-neck cancers, some lung cancers), etc.

  • The epothilones, e.g. Ixabepilone, work in a similar way to the taxanes.
  • Vinorelbine, Nocodazole, vincristine, and colchicine have the opposite effect, blocking the polymerization of tubulin into microtubules.
  • Eribulin binds to the (+) growing end of the microtubules. Eribulin exerts its anticancer effects by triggering apoptosis of cancer cells following prolonged and irreversible mitotic blockade.

Expression of β3-tubulin has been reported to alter cellular responses to drug-induced suppression of microtubule dynamics. In general the dynamics are normally suppressed by low, subtoxic concentrations of microtubule drugs that also inhibit cell migration. However, incorporating β3-tubulin into microtubules increases the concentration of drug that is needed to suppress dynamics and inhibit cell migration. Thus, tumors that express β3-tubulin are not only resistant to the cytotoxic effects of microtubule targeted drugs, but also to their ability to suppress tumor metastasis.[48] Moreover, expression of β3-tubulin also counteracts the ability of these drugs to inhibit angiogenesis which is normally another important facet of their action.[49]

Microtubule polymers are extremely sensitive to various environmental effects. Very low levels of free calcium can destabilize microtubules and this prevented early researchers from studying the polymer in vitro.[12] Cold temperatures also cause rapid depolymerization of microtubules. In contrast, heavy water promotes microtubule polymer stability.[50]

Proteins that interact with microtubules

Microtubule-associated proteins (MAPs)

MAPs have been shown to play a crucial role in the regulation of microtubule dynamics in-vivo. The rates of microtubule polymerization, depolymerization, and catastrophe vary depending on which microtubule-associated proteins (MAPs) are present. The originally identified MAPs from brain tissue can be classified into two groups based on their molecular weight. This first class comprises MAPs with a molecular weight below 55-62 kDa, and are called τ (tau) proteins. In-vitro, tau proteins have been shown to directly bind microtubules, promote nucleation and prevent disassembly, and to induce the formation of parallel arrays.[51] Additionally, tau proteins have also been shown to stabilize microtubules in axons and have been implicated in Alzheimer's disease.[52] The second class is composed of MAPs with a molecular weight of 200-1000 kDa, of which there are four known types: MAP-1, MAP-2, MAP-3 and MAP-4. MAP-1 proteins consists of a set of three different proteins: A, B and C. The C protein plays an important role in the retrograde transport of vesicles and is also known as cytoplasmic dynein. MAP-2 proteins are located in the dendrites and in the body of neurons, where they bind with other cytoskeletal filaments. The MAP-4 proteins are found in the majority of cells and stabilize microtubules. In addition to MAPs that have a stabilizing effect on microtubule structure, other MAPs can have a destabilizing effect either by cleaving or by inducing depolymerization of microtubules. Three proteins called katanin, spastin, and fidgetin have been observed to regulate the number and length of microtubules via their destabilizing activities. Furthermore, CRACD-like protein is predicted to be localized to the microtubules.[53]

MAPs are determinants of different cytoskeletal forms of axons and dendrites, with microtubules being farther apart in the dendrites [54]

Plus-end tracking proteins (+TIPs)

Plus end tracking proteins are MAP proteins which bind to the tips of growing microtubules and play an important role in regulating microtubule dynamics. For example, +TIPs have been observed to participate in the interactions of microtubules with chromosomes during mitosis. The first MAP to be identified as a +TIP was CLIP170 (cytoplasmic linker protein), which has been shown to play a role in microtubule depolymerization rescue events. Additional examples of +TIPs include EB1, EB2, EB3, p150Glued, Dynamitin, Lis1, CLIP115, CLASP1, and CLASP2.

Motor proteins

A cytoplasmic dynein motor bound to a microtubule.
A kinesin molecule bound to a microtubule.

Microtubules can act as substrates for motor proteins that are involved in important cellular functions such as vesicle trafficking and cell division. Unlike other microtubule-associated proteins, motor proteins utilize the energy from ATP hydrolysis to generate mechanical work that moves the protein along the substrate. The major motor proteins that interact with microtubules are kinesin, which usually moves toward the (+) end of the microtubule, and dynein, which moves toward the (−) end.

  • Dynein is composed of two identical heavy chains, which make up two large globular head domains, and a variable number of intermediate and light chains. Dynein-mediated transport takes place from the (+) end towards the (-) end of the microtubule. ATP hydrolysis occurs in the globular head domains, which share similarities with the AAA+ (ATPase associated with various cellular activities) protein family. ATP hydrolysis in these domains is coupled to movement along the microtubule via the microtubule-binding domains. Dynein transports vesicles and organelles throughout the cytoplasm. In order to do this, dynein molecules bind organelle membranes via a protein complex that contains a number of elements including dynactin.
  • Kinesin has a similar structure to dynein. Kinesin is involved in the transport of a variety of intracellular cargoes, including vesicles, organelles, protein complexes, and mRNAs toward the microtubule's (+) end.[55]

Some viruses (including retroviruses, herpesviruses, parvoviruses, and adenoviruses) that require access to the nucleus to replicate their genomes attach to motor proteins.

Mitosis

Centrosomes

A 3D diagram of a centriole. Each circle represents one microtubule. In total there are 27 microtubules organized into 9 bundles of 3.

The centrosome is the main MTOC (microtubule organizing center) of the cell during mitosis. Each centrosome is made up of two cylinders called centrioles, oriented at right angles to each other. The centriole is formed from 9 main microtubules, each having two partial microtubules attached to it. Each centriole is approximately 400 nm long and around 200 nm in circumference.[56]

The centrosome is critical to mitosis as most microtubules involved in the process originate from the centrosome. The minus ends of each microtubule begin at the centrosome, while the plus ends radiate out in all directions. Thus the centrosome is also important in maintaining the polarity of microtubules during mitosis.[57]

Most cells only have one centrosome for most of their cell cycle, however, right before mitosis, the centrosome duplicates, and the cell contains two centrosomes.[58] Some of the microtubules that radiate from the centrosome grow directly away from the sister centrosome. These microtubules are called astral microtubules. With the help of these astral microtubules the centrosomes move away from each other towards opposite sides of the cell. Once there, other types of microtubules necessary for mitosis, including interpolar microtubules and K-fibers can begin to form.[59]

A final important note about the centrosomes and microtubules during mitosis is that while the centrosome is the MTOC for the microtubules necessary for mitosis, research has shown that once the microtubules themselves are formed and in the correct place the centrosomes themselves are not needed for mitosis to occur.[60]

Microtubule subclasses

This diagram depicts the organization of a typical mitotic spindle found in animal cells. Shown here are the three main types of microtubules during mitosis and how they are oriented in the cell and the mitotic spindle.

Astral microtubules are a subclass of microtubules which only exist during and around mitosis. They originate from the centrosome, but do not interact with the chromosomes, kinetochores, or with the microtubules originating from the other centrosome.[61] Instead their microtubules radiate towards the cell membrane. Once there they interact with specific motor proteins which create force that pull the microtubules, and thus the entire centrosome towards the cell membrane. As stated above, this helps the centrosomes orient themselves away from each other in the cell. However these astral microtubules do not interact with the mitotic spindle itself. Experiments have shown that without these astral microtubules, the mitotic spindle can form, however its orientation in the cell is not always correct and thus mitosis does not occur as effectively.[62] Another key function of the astral microtubules is to aid in cytokinesis. Astral microtubules interact with motor proteins at the cell membrane to pull the spindle and the entire cell apart once the chromosomes have been replicated.

Interpolar/Polar microtubules are a class of microtubules which also radiate out from the centrosome during mitosis. These microtubules radiate towards the mitotic spindle, unlike astral microtubules. Interpolar microtubules are both the most abundant and dynamic subclass of microtubules during mitosis. Around 95 percent of microtubules in the mitotic spindle can be characterized as interpolar. Furthermore, the half life of these microtubules is extremely short as it is less than one minute.[63] Interpolar microtubules that do not attach to the kinetochores can aid in chromosome congregation through lateral interaction with the kinetochores.[64]

K fibers/Kinetochore microtubules are the third important subclass of mitotic microtubules. These microtubules form direct connections with the kinetochores in the mitotic spindle. Each K fiber is composed of 20–40 parallel microtubules, forming a strong tube which is attached at one end to the centrosome and on the other to the kinetochore, located in the center of each chromosome. Since each centrosome has a K fiber connecting to each pair of chromosomes, the chromosomes become tethered in the middle of the mitotic spindle by the K fibers. K fibers have a much longer half life than interpolar microtubules, at between 4 and 8 minutes.[65] During the end of mitoses, the microtubules forming each K fiber begin to disassociate, thus shorting the K fibers. As the K fibers shorten the pair chromosomes are pulled apart right before cytokinesis. Previously, some researchers believed that K fibers form at their minus end originating from the centrosome just like other microtubules, however, new research has pointed to a different mechanism. In this new mechanism, the K fibers are initially stabilized at their plus end by the kinetochores and grow out from there. The minus end of these K fibers eventually connect to an existing Interpolar microtubule and are eventually connected to the centrosome in this way.[66]

Microtubule nuclear in the mitotic spindle

Most of the microtubules that form the mitotic spindle originate from the centrosome. Originally it was thought that all of these microtubules originated from the centrosome via a method called search and capture, described in more detail in a section above, however new research has shown that there are addition means of microtubule nucleation during mitosis. One of the most important of these additional means of microtubule nucleation is the RAN-GTP pathway. RAN-GTP associates with chromatin during mitosis to create a gradient that allows for local nucleation of microtubules near the chromosomes. Furthermore, a second pathway known as the augmin/HAUS complex (some organisms use the more studied augmin complex, while others such as humans use an analogous complex called HAUS) acts an additional means of microtubule nucleation in the mitotic spindle.[66]

Functions

Cell migration

Microtubule plus ends are often localized to particular structures. In polarized interphase cells, microtubules are disproportionately oriented from the MTOC toward the site of polarity, such as the leading edge of migrating fibroblasts. This configuration is thought to help deliver microtubule-bound vesicles from the Golgi to the site of polarity.

Dynamic instability of microtubules is also required for the migration of most mammalian cells that crawl.[67] Dynamic microtubules regulate the levels of key G-proteins such as RhoA[68] and Rac1,[69] which regulate cell contractility and cell spreading. Dynamic microtubules are also required to trigger focal adhesion disassembly, which is necessary for migration.[70] It has been found that microtubules act as "struts" that counteract the contractile forces that are needed for trailing edge retraction during cell movement. When microtubules in the trailing edge of cell are dynamic, they are able to remodel to allow retraction. When dynamics are suppressed, microtubules cannot remodel and, therefore, oppose the contractile forces.[47] The morphology of cells with suppressed microtubule dynamics indicate that cells can extend the front edge (polarized in the direction of movement), but have difficulty retracting their trailing edge.[71] On the other hand, high drug concentrations, or microtubule mutations that depolymerize the microtubules, can restore cell migration but there is a loss of directionality. It can be concluded that microtubules act both to restrain cell movement and to establish directionality.

Cilia and flagella

Microtubules have a major structural role in eukaryotic cilia and flagella. Cilia and flagella always extend directly from a MTOC, in this case termed the basal body. The action of the dynein motor proteins on the various microtubule strands that run along a cilium or flagellum allows the organelle to bend and generate force for swimming, moving extracellular material, and other roles. Prokaryotes possess tubulin-like proteins including FtsZ. However, prokaryotic flagella are entirely different in structure from eukaryotic flagella and do not contain microtubule-based structures.

Development

The cytoskeleton formed by microtubules is essential to the morphogenetic process of an organism's development. For example, a network of polarized microtubules is required within the oocyte of Drosophila melanogaster during its embryogenesis in order to establish the axis of the egg. Signals sent between the follicular cells and the oocyte (such as factors similar to epidermal growth factor) cause the reorganization of the microtubules so that their (-) ends are located in the lower part of the oocyte, polarizing the structure and leading to the appearance of an anterior-posterior axis.[72] This involvement in the body's architecture is also seen in mammals.[73]

Another area where microtubules are essential is the development of the nervous system in higher vertebrates, where tubulin's dynamics and those of the associated proteins (such as the microtubule-associated proteins) are finely controlled during the development of the nervous system.[74]

Gene regulation

The cellular cytoskeleton is a dynamic system that functions on many different levels: In addition to giving the cell a particular form and supporting the transport of vesicles and organelles, it can also influence gene expression. The signal transduction mechanisms involved in this communication are little understood. However, the relationship between the drug-mediated depolymerization of microtubules, and the specific expression of transcription factors has been described, which has provided information on the differential expression of the genes depending on the presence of these factors.[75] This communication between the cytoskeleton and the regulation of the cellular response is also related to the action of growth factors: for example, this relation exists for connective tissue growth factor.[76]

See also

References

  1. ↑ "Digital Downloads". PurSolutions. Retrieved 2020-02-20.
  2. ↑ Ledbetter MC, Porter KR (1963). "A "microtubule" in plant cell fine structure". Journal of Cell Biology. 19 (1): 239–50. doi:10.1083/jcb.19.1.239. PMC 2106853. PMID 19866635.
  3. ↑ Chalfie M, Thomson JN (1979). "Organization of neuronal microtubules in the nematode Caenorhabditis elegans". Journal of Cell Biology. 82 (1): 278–89. doi:10.1083/jcb.82.1.278. PMC 2110421. PMID 479300.
  4. ↑ Diwan JJ (2006). "Microtubules". Rensselaer Polytechnic Institute. Archived from the original on 2014-02-06. Retrieved 2014-02-24.
  5. ↑ Vale RD (February 2003). "The molecular motor toolbox for intracellular transport". Cell. 112 (4): 467–80. doi:10.1016/S0092-8674(03)00111-9. PMID 12600311. S2CID 15100327.
  6. ↑ Howard J, Hyman AA (February 2007). "Microtubule polymerases and depolymerases". Current Opinion in Cell Biology. 19 (1): 31–5. doi:10.1016/j.ceb.2006.12.009. PMID 17184986.
  7. ↑ Jiang S, Narita A, Popp D, Ghoshdastider U, Lee LJ, Srinivasan R, Balasubramanian MK, Oda T, Koh F, Larsson M, Robinson RC (March 2016). "Novel actin filaments from Bacillus thuringiensis form nanotubules for plasmid DNA segregation". Proceedings of the National Academy of Sciences of the United States of America. 113 (9): E1200-5. Bibcode:2016PNAS..113E1200J. doi:10.1073/pnas.1600129113. PMC 4780641. PMID 26873105.
  8. ↑ Wayne, R. 2009. Plant Cell Biology: From Astronomy to Zoology. Amsterdam: Elsevier/Academic Press, p. 165.
  9. ↑ Cooper GM (2000). "Microtubule Motors and Movements". The Cell: A Molecular Approach. 2nd Edition. Retrieved 2019-03-12.
  10. ↑ Kapoor V, Hirst WG, Hentschel C, Preibisch S, Reber S (March 2019). "MTrack: Automated Detection, Tracking, and Analysis of Dynamic Microtubules". Scientific Reports. 9 (1): 3794. Bibcode:2019NatSR...9.3794K. doi:10.1038/s41598-018-37767-1. PMC 6405942. PMID 30846705.
  11. ↑ Löwe J, Li H, Downing KH, Nogales E (November 2001). "Refined structure of alpha beta-tubulin at 3.5 A resolution". Journal of Molecular Biology. 313 (5): 1045–57. doi:10.1006/jmbi.2001.5077. PMID 11700061.
  12. 1 2 3 Weisenberg RC (September 1972). "Microtubule formation in vitro in solutions containing low calcium concentrations". Science. 177 (4054): 1104–5. Bibcode:1972Sci...177.1104W. doi:10.1126/science.177.4054.1104. PMID 4626639. S2CID 34875893.
  13. ↑ Desai A, Mitchison TJ (1997). "Microtubule polymerization dynamics". Annual Review of Cell and Developmental Biology. 13: 83–117. doi:10.1146/annurev.cellbio.13.1.83. PMID 9442869.
  14. ↑ Desai, A.; Mitchison, T. J. (1997). "Microtubule polymerization dynamics". Annual Review of Cell and Developmental Biology. 13: 83–117. doi:10.1146/annurev.cellbio.13.1.83. ISSN 1081-0706. PMID 9442869.
  15. ↑ Chaaban S, Brouhard GJ (2017). "A microtubule bestiary: structural diversity in tubulin polymers". Molecular Biology of the Cell. 28 (22): 2924–31. doi:10.1091/mbc.E16-05-0271. PMC 5662251. PMID 29084910.
  16. ↑ Chrétien D, Metoz F, Verde F, Karsenti E, Wade RH (June 1992). "Lattice defects in microtubules: protofilament numbers vary within individual microtubules". Journal of Cell Biology. 117 (5): 1031–40. doi:10.1083/jcb.117.5.1031. PMC 2289483. PMID 1577866.
  17. ↑ Walker RA, O'Brien ET, Pryer NK, Soboeiro MF, Voter WA, Erickson HP, Salmon ED (October 1988). "Dynamic instability of individual microtubules analyzed by video light microscopy: rate constants and transition frequencies". The Journal of Cell Biology. 107 (4): 1437–48. CiteSeerX 10.1.1.525.507. doi:10.1083/jcb.107.4.1437. PMC 2115242. PMID 3170635.
  18. ↑ Sui H, Downing KH (August 2010). "Structural basis of interprotofilament interaction and lateral deformation of microtubules". Structure. 18 (8): 1022–31. doi:10.1016/j.str.2010.05.010. PMC 2976607. PMID 20696402.
  19. ↑ Bassen DM, Hou Y, Bowser SS, Banavali NK (August 2016). "Maintenance of electrostatic stabilization in altered tubulin lateral contacts may facilitate formation of helical filaments in foraminifera". Scientific Reports. 6: 31723. Bibcode:2016NatSR...631723B. doi:10.1038/srep31723. PMC 4990898. PMID 27539392.
  20. ↑ Nogales E (2000). "Structural insights into microtubule function". Annual Review of Biochemistry. 69: 277–302. doi:10.1146/annurev.biochem.69.1.277. PMID 10966460.
  21. ↑ Schlieper D, Oliva MA, Andreu JM, Löwe J (June 2005). "Structure of bacterial tubulin BtubA/B: evidence for horizontal gene transfer". Proceedings of the National Academy of Sciences of the United States of America. 102 (26): 9170–5. Bibcode:2005PNAS..102.9170S. doi:10.1073/pnas.0502859102. PMC 1166614. PMID 15967998.
  22. ↑ Pilhofer M, Ladinsky MS, McDowall AW, Petroni G, Jensen GJ (December 2011). "Microtubules in bacteria: Ancient tubulins build a five-protofilament homolog of the eukaryotic cytoskeleton". PLOS Biology. 9 (12): e1001213. doi:10.1371/journal.pbio.1001213. PMC 3232192. PMID 22162949.
  23. ↑ "Medical Definition of Neurotubules". www.merriam-webster.com.
  24. ↑ Zhao B, Meka DP, Scharrenberg R, König T, Schwanke B, Kobler O, Windhorst S, Kreutz MR, Mikhaylova M, Calderon de Anda F (August 2017). "Microtubules Modulate F-actin Dynamics during Neuronal Polarization". Scientific Reports. 7 (1): 9583. Bibcode:2017NatSR...7.9583Z. doi:10.1038/s41598-017-09832-8. PMC 5575062. PMID 28851982.
  25. ↑ Bartolini F, Gundersen GG (October 2006). "Generation of noncentrosomal microtubule arrays". Journal of Cell Science. 119 (Pt 20): 4155–63. doi:10.1242/jcs.03227. PMID 17038542.
  26. ↑ Desai A, Mitchison TJ (1997). "Microtubule polymerization dynamics". Annual Review of Cell and Developmental Biology. 13: 83–117. doi:10.1146/annurev.cellbio.13.1.83. PMID 9442869.
  27. ↑ Vinogradova T, Miller PM, Kaverina I (July 2009). "Microtubule network asymmetry in motile cells: role of Golgi-derived array". Cell Cycle. 8 (14): 2168–74. doi:10.4161/cc.8.14.9074. PMC 3163838. PMID 19556895.
  28. ↑ Uehara R, Nozawa RS, Tomioka A, Petry S, Vale RD, Obuse C, Goshima G (April 2009). "The augmin complex plays a critical role in spindle microtubule generation for mitotic progression and cytokinesis in human cells". Proceedings of the National Academy of Sciences of the United States of America. 106 (17): 6998–7003. Bibcode:2009PNAS..106.6998U. doi:10.1073/pnas.0901587106. PMC 2668966. PMID 19369198.
  29. ↑ Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P (2002). "The Self-Assembly and Dynamic Structure of Cytoskeletal Filaments". Molecular Biology of the Cell (4th ed.). New York: Garland Science.
  30. ↑ Karp G (2005). Cell and Molecular Biology: Concepts and Experiments. USA: John Wiley & Sons. p. 355. ISBN 978-0-471-46580-5.
  31. ↑ Weisenberg RC, Deery WJ, Dickinson PJ (September 1976). "Tubulin-nucleotide interactions during the polymerization and depolymerization of microtubules". Biochemistry. 15 (19): 4248–54. doi:10.1021/bi00664a018. PMID 963034.
  32. ↑ Mitchison T, Kirschner M (1984). "Dynamic instability of microtubule growth". Nature. 312 (5991): 237–42. Bibcode:1984Natur.312..237M. doi:10.1038/312237a0. PMID 6504138. S2CID 30079133.
  33. ↑ Kirschner M, Mitchison T (May 1986). "Beyond self-assembly: from microtubules to morphogenesis". Cell. 45 (3): 329–42. doi:10.1016/0092-8674(86)90318-1. PMID 3516413. S2CID 36994346.
  34. ↑ Cheeseman IM, Desai A (January 2008). "Molecular architecture of the kinetochore-microtubule interface". Nature Reviews. Molecular Cell Biology. 9 (1): 33–46. doi:10.1038/nrm2310. PMID 18097444. S2CID 34121605.
  35. 1 2 Infante AS, Stein MS, Zhai Y, Borisy GG, Gundersen GG (November 2000). "Detyrosinated (Glu) microtubules are stabilized by an ATP-sensitive plus-end cap". Journal of Cell Science. 113 (22): 3907–19. doi:10.1242/jcs.113.22.3907. PMID 11058078.
  36. ↑ Palazzo AF, Cook TA, Alberts AS, Gundersen GG (August 2001). "mDia mediates Rho-regulated formation and orientation of stable microtubules". Nature Cell Biology. 3 (8): 723–9. doi:10.1038/35087035. PMID 11483957. S2CID 7374170.
  37. ↑ Wen Y, Eng CH, Schmoranzer J, Cabrera-Poch N, Morris EJ, Chen M, Wallar BJ, Alberts AS, Gundersen GG (September 2004). "EB1 and APC bind to mDia to stabilize microtubules downstream of Rho and promote cell migration". Nature Cell Biology. 6 (9): 820–30. doi:10.1038/ncb1160. PMID 15311282. S2CID 29214110.
  38. 1 2 Janke C, Bulinski JC (November 2011). "Post-translational regulation of the microtubule cytoskeleton: mechanisms and functions". Nature Reviews. Molecular Cell Biology. 12 (12): 773–86. doi:10.1038/nrm3227. PMID 22086369. S2CID 5969290.
  39. 1 2 3 Garnham CP, Roll-Mecak A (July 2012). "The chemical complexity of cellular microtubules: tubulin post-translational modification enzymes and their roles in tuning microtubule functions". Cytoskeleton. 69 (7): 442–63. doi:10.1002/cm.21027. PMC 3459347. PMID 22422711.
  40. ↑ Ersfeld K, Wehland J, Plessmann U, Dodemont H, Gerke V, Weber K (February 1993). "Characterization of the tubulin-tyrosine ligase". The Journal of Cell Biology. 120 (3): 725–32. doi:10.1083/jcb.120.3.725. PMC 2119537. PMID 8093886.
  41. ↑ Paturle-Lafanechère L, Eddé B, Denoulet P, Van Dorsselaer A, Mazarguil H, Le Caer JP, Wehland J, Job D (October 1991). "Characterization of a major brain tubulin variant which cannot be tyrosinated". Biochemistry. 30 (43): 10523–8. doi:10.1021/bi00107a022. PMID 1931974.
  42. ↑ Kalebic N, Sorrentino S, Perlas E, Bolasco G, Martinez C, Heppenstall PA (2013-06-10). "αTAT1 is the major α-tubulin acetyltransferase in mice". Nature Communications. 4: 1962. Bibcode:2013NatCo...4.1962K. doi:10.1038/ncomms2962. PMID 23748901.
  43. ↑ Hubbert C, Guardiola A, Shao R, Kawaguchi Y, Ito A, Nixon A, Yoshida M, Wang XF, Yao TP (May 2002). "HDAC6 is a microtubule-associated deacetylase". Nature. 417 (6887): 455–8. Bibcode:2002Natur.417..455H. doi:10.1038/417455a. PMID 12024216. S2CID 4373254.
  44. ↑ Carmona, Bruno; Marinho, H. Susana; Matos, Catarina Lopes; Nolasco, Sofia; Soares, Helena (2023). "Tubulin Post-Translational Modifications: The Elusive Roles of Acetylation". Biology. 12 (4): 561. doi:10.3390/biology12040561. ISSN 2079-7737. PMC 10136095. PMID 37106761.
  45. ↑ Audebert S, Desbruyères E, Gruszczynski C, Koulakoff A, Gros F, Denoulet P, Eddé B (June 1993). "Reversible polyglutamylation of alpha- and beta-tubulin and microtubule dynamics in mouse brain neurons". Molecular Biology of the Cell. 4 (6): 615–26. doi:10.1091/mbc.4.6.615. PMC 300968. PMID 8104053.
  46. ↑ Ganguly A, Yang H, Cabral F (November 2010). "Paclitaxel-dependent cell lines reveal a novel drug activity". Molecular Cancer Therapeutics. 9 (11): 2914–23. doi:10.1158/1535-7163.MCT-10-0552. PMC 2978777. PMID 20978163.
  47. 1 2 Yang H, Ganguly A, Cabral F (October 2010). "Inhibition of cell migration and cell division correlates with distinct effects of microtubule inhibiting drugs". The Journal of Biological Chemistry. 285 (42): 32242–50. doi:10.1074/jbc.M110.160820. PMC 2952225. PMID 20696757.
  48. ↑ Altonsy, Mohammed; Ganguly, Anutosh; Amrein, Matthias; Surmanowicz, Philip; Li, Shu; Lauzon, Gilles (Mar 2020). "Beta3-Tubulin Is Critical for Microtubule Dynamics, Cell Cycle Regulation, and Spontaneous Release of Microvesicles in Human Malignant Melanoma Cells (A375)". International Journal of Molecular Sciences. 21 (5): 1656. doi:10.3390/ijms21051656. PMC 7084453. PMID 32121295.
  49. ↑ Ganguly, Anutosh; Yang, Hailing; Fernando, Gabral (May 2011). "Class III β-Tubulin Counteracts the Ability of Paclitaxel to Inhibit Cell Migration". Oncotarget. 2 (5): 368–377. doi:10.18632/oncotarget.250. PMC 3248193. PMID 21576762.
  50. ↑ Burgess J, Northcote DH (September 1969). "Action of colchicine and heavy water on the polymerization of microtubules in wheat root meristem". Journal of Cell Science. 5 (2): 433–51. doi:10.1242/jcs.5.2.433. PMID 5362335.
  51. ↑ Mandelkow E, Mandelkow EM (February 1995). "Microtubules and microtubule-associated proteins". Current Opinion in Cell Biology. 7 (1): 72–81. doi:10.1016/0955-0674(95)80047-6. PMID 7755992.
  52. ↑ Bramblett GT, Goedert M, Jakes R, Merrick SE, Trojanowski JQ, Lee VM (June 1993). "Abnormal tau phosphorylation at Ser396 in Alzheimer's disease recapitulates development and contributes to reduced microtubule binding". Neuron. 10 (6): 1089–99. doi:10.1016/0896-6273(93)90057-X. PMID 8318230. S2CID 23180847.
  53. ↑ "The Human Protein Atlas". www.proteinatlas.org. Archived from the original on 2017-05-01. Retrieved 2017-04-27.
  54. ↑ Hirokawa, N (1994). "The neuronal cytoskeleton: roles in neuronal morphogenesis and organelle transport". Molecular Neurobiology: Mechanisms Common to Brain, Skin and Immune System. Series: Progress in Clinical and Biological Research. Willey-Liss, Inc. 390: 117–143. PMID 7536943.
  55. ↑ Hirokawa N, Noda Y, Tanaka Y, Niwa S (October 2009). "Kinesin superfamily motor proteins and intracellular transport". Nature Reviews. Molecular Cell Biology. 10 (10): 682–96. doi:10.1038/nrm2774. PMID 19773780. S2CID 18129292.
  56. ↑ Marshall WF, Rosenbaum JL (March 1999). "Cell division: The renaissance of the centriole". Current Biology. 9 (6): R218–20. doi:10.1016/s0960-9822(99)80133-x. PMID 10209087. S2CID 16951268.
  57. ↑ Pereira G, Schiebel E (February 1997). "Centrosome-microtubule nucleation". Journal of Cell Science. 110 (Pt 3): 295–300. doi:10.1242/jcs.110.3.295. PMID 9057082.
  58. ↑ Hinchcliffe EH, Sluder G (May 2001). ""It takes two to tango": understanding how centrosome duplication is regulated throughout the cell cycle". Genes & Development. 15 (10): 1167–81. doi:10.1101/gad.894001. PMID 11358861.
  59. ↑ Forth S, Kapoor TM (June 2017). "The mechanics of microtubule networks in cell division". The Journal of Cell Biology. 216 (6): 1525–1531. doi:10.1083/jcb.201612064. PMC 5461028. PMID 28490474.
  60. ↑ Khodjakov, A., Cole, R. W., Oakley, B. R. and Rieder, C. L. (2000). "Centrosome-independent mitotic spindle formation in vertebrates". Curr. Biol. 10, 59–67. doi:10.1016/S0960-9822(99)00276-6.
  61. ↑ Rosenblatt J (March 2005). "Spindle assembly: asters part their separate ways". Nature Cell Biology. 7 (3): 219–22. doi:10.1038/ncb0305-219. PMID 15738974. S2CID 8082479.
  62. ↑ Knoblich JA (December 2010). "Asymmetric cell division: recent developments and their implications for tumour biology". Nature Reviews. Molecular Cell Biology. 11 (12): 849–60. doi:10.1038/nrm3010. PMC 3941022. PMID 21102610.
  63. ↑ Zhai Y, Kronebusch PJ, Borisy GG (November 1995). "Kinetochore microtubule dynamics and the metaphase-anaphase transition". The Journal of Cell Biology. 131 (3): 721–34. doi:10.1083/jcb.131.3.721. PMC 2120628. PMID 7593192.
  64. ↑ Cai S, O'Connell CB, Khodjakov A, Walczak CE (July 2009). "Chromosome congression in the absence of kinetochore fibres". Nature Cell Biology. 11 (7): 832–8. doi:10.1038/ncb1890. PMC 2895821. PMID 19525938.
  65. ↑ Bakhoum SF, Thompson SL, Manning AL, Compton DA (January 2009). "Genome stability is ensured by temporal control of kinetochore-microtubule dynamics". Nature Cell Biology. 11 (1): 27–35. doi:10.1038/ncb1809. PMC 2614462. PMID 19060894.
  66. 1 2 Meunier S, Vernos I (June 2012). "Microtubule assembly during mitosis - from distinct origins to distinct functions?". Journal of Cell Science. 125 (Pt 12): 2805–14. doi:10.1242/jcs.092429. PMID 22736044.
  67. ↑ Mikhailov A, Gundersen GG (1998). "Relationship between microtubule dynamics and lamellipodium formation revealed by direct imaging of microtubules in cells treated with nocodazole or taxol". Cell Motility and the Cytoskeleton. 41 (4): 325–40. doi:10.1002/(SICI)1097-0169(1998)41:4<325::AID-CM5>3.0.CO;2-D. PMID 9858157.
  68. ↑ Ren XD, Kiosses WB, Schwartz MA (February 1999). "Regulation of the small GTP-binding protein Rho by cell adhesion and the cytoskeleton". The EMBO Journal. 18 (3): 578–85. doi:10.1093/emboj/18.3.578. PMC 1171150. PMID 9927417.
  69. ↑ Waterman-Storer CM, Worthylake RA, Liu BP, Burridge K, Salmon ED (May 1999). "Microtubule growth activates Rac1 to promote lamellipodial protrusion in fibroblasts". Nature Cell Biology. 1 (1): 45–50. doi:10.1038/9018. PMID 10559863. S2CID 26321103.
  70. ↑ Ezratty EJ, Partridge MA, Gundersen GG (June 2005). "Microtubule-induced focal adhesion disassembly is mediated by dynamin and focal adhesion kinase". Nature Cell Biology. 7 (6): 581–90. doi:10.1038/ncb1262. PMID 15895076. S2CID 37153935.
  71. ↑ Ganguly A, Yang H, Sharma R, Patel KD, Cabral F (December 2012). "The role of microtubules and their dynamics in cell migration". The Journal of Biological Chemistry. 287 (52): 43359–69. doi:10.1074/jbc.M112.423905. PMC 3527923. PMID 23135278.
  72. ↑ van Eeden F, St Johnston D (August 1999). "The polarisation of the anterior-posterior and dorsal-ventral axes during Drosophila oogenesis". Current Opinion in Genetics & Development. 9 (4): 396–404. doi:10.1016/S0959-437X(99)80060-4. PMID 10449356.
  73. ↑ Beddington RS, Robertson EJ (January 1999). "Axis development and early asymmetry in mammals". Cell. 96 (2): 195–209. doi:10.1016/S0092-8674(00)80560-7. PMID 9988215. S2CID 16264083.
  74. ↑ Tucker RP (1990). "The roles of microtubule-associated proteins in brain morphogenesis: a review". Brain Research. Brain Research Reviews. 15 (2): 101–20. doi:10.1016/0165-0173(90)90013-E. PMID 2282447. S2CID 12641708.
  75. ↑ Rosette C, Karin M (March 1995). "Cytoskeletal control of gene expression: depolymerization of microtubules activates NF-kappa B". The Journal of Cell Biology. 128 (6): 1111–9. doi:10.1083/jcb.128.6.1111. PMC 2120413. PMID 7896875.
  76. ↑ Ott C, Iwanciw D, Graness A, Giehl K, Goppelt-Struebe M (November 2003). "Modulation of the expression of connective tissue growth factor by alterations of the cytoskeleton". The Journal of Biological Chemistry. 278 (45): 44305–11. doi:10.1074/jbc.M309140200. PMID 12951326.
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