D-loop replication is a proposed process by which circular DNA like chloroplasts and mitochondria replicate their genetic material. An important component of understanding D-loop replication is that many chloroplasts and mitochondria have a single circular chromosome like bacteria instead of the linear chromosomes found in eukaryotes. However, many chloroplasts and mitochondria have a linear chromosome, and D-loop replication is not important in these organelles. Also, not all circular genomes use D-loop replication as the process of replicating its genome.[1]

In many organisms, one strand of DNA in the plasmid comprises heavier nucleotides (relatively more purines: adenine and guanine). This strand is called the H (heavy) strand. The L (light) strand comprises lighter nucleotides (pyrimidines: thymine and cytosine). Replication begins with replication of the heavy strand starting at the D-loop (also known as the control region). A D-loop is a short portion in circular DNA that has three strands instead of two. The middle strand, which is complementary to the light strand, displaces the heavy strand and forms a displacement loop (D-loop).[2] Circular DNA is stable with this small D-loop and can remain in this formation, but the middle strand, or the displacing strand, is replaced frequently due to its short half-life, and is very energetically expensive to the cell.[3][4] When diagramed, the resulting structure looks like the letter D. The D-loop was first discovered in 1971 when researchers noticed that many DNA in the mitochondria they were examining under microscope contained a short segment that was tripled stranded.[2]

Replication process

Each D-loop contains an origin of replication for the heavy strand. Full circular DNA replication is initiated at that origin and replicates in only one direction. The middle strand in the D-loop can be removed and a new one will be synthesized that is not terminated until the heavy strand is fully replicated, or the middle strand can serve as a primer for the heavy strand replication. As the heavy strand replication reaches the origin of replication for the light strand, a new light strand will be synthesized in the opposite direction as the heavy strand.[3][5][6] There is more than one proposed process through which D-loop replication occurs, but in all of the models, these steps are agreed upon. The portions not agreed upon are what is the importance of maintaining a D-loop when replication is not in progress, because it is energetically expensive to the cell, and what mechanisms, during replication, preserve the detached strand of DNA that is waiting to be replicated.[7][8][9]

Importance

The D-loop region is important for phylogeographic studies. Because the region does not code for any genes, it is not imperative for this region to remain conserved over time, therefore, it is free to mutate with only a few selective limitations on size and heavy/light strand factors. The mutation rate is among the fastest of anywhere in either the nuclear or mitochondrial genomes in animals. Using these mutations in the D-loop, recent and rapid evolutionary changes can effectively be tracked such as within species and among very closely related species. Due to the high mutation rate, it is not effective in tracking evolutionary changes that are not recent. This is a very common use of the D-loop in genomics.[10]

One example of the use of D-loop mutations in phylogeographic studies was the phylogeny assembled using the highly unstudied red deer on the Iberian peninsula. Scientist tracked the D-loop polymorphisms within these red deer and determined the genetic relationship that these deer had among each other. They were also able to determine the relationships, based on D-loop similarities and differences, between these red deer and other deer throughout Europe.[11] In another example, scientist used the variations in the D-loop, along with microsatellite markers, to study and map out the genetic diversity among goats in Sri Lanka.[12]

See also

References

  1. ↑ Russell, P. J. 2002. iGenetics.Benjamin Cummings, San Francisco
  2. 1 2 Kasamatsu, Harumi; Robberson, Donald L.; Vinograd, Jerome (1971). "A novel closed-circular mitochondrial DNA with properties of a replicating intermediate". Proceedings of the National Academy of Sciences. 68 (9): 2252–2257. Bibcode:1971PNAS...68.2252K. doi:10.1073/pnas.68.9.2252. PMC 389395. PMID 5289384.
  3. 1 2 Nicholls, Thomas J.; Minczuk, Michal (2014). "In D-loop: 40 years of mitochondrial 7S DNA". Experimental Gerontology. 56: 175–181. doi:10.1016/j.exger.2014.03.027. PMID 24709344. S2CID 140205074.
  4. ↑ Doda, Jackie N.; Wright, Catharine T.; Clayton, David A. (1981). "Elongation of displacement-loop strands in human and mouse mitochondrial DNA is arrested near specific template sequences". Proceedings of the National Academy of Sciences. 78 (10): 6116–6120. Bibcode:1981PNAS...78.6116D. doi:10.1073/pnas.78.10.6116. PMC 348988. PMID 6273850.
  5. ↑ Clayton, David A (1982). "Replication of animal mitochondrial DNA". Cell. 28 (4): 693–705. doi:10.1016/0092-8674(82)90049-6. PMID 6178513. S2CID 12682150.
  6. ↑ Chang, D. D.; Clayton, D. A. (1985-01-01). "Priming of human mitochondrial DNA replication occurs at the light-strand promoter". Proceedings of the National Academy of Sciences. 82 (2): 351–355. Bibcode:1985PNAS...82..351C. doi:10.1073/pnas.82.2.351. ISSN 0027-8424. PMC 397036. PMID 2982153.
  7. ↑ Leslie, Mitch (2007-01-15). "Thrown for a D-loop". The Journal of Cell Biology. 176 (2): 129a. doi:10.1083/jcb.1762iti3. ISSN 0021-9525. PMC 2063944.
  8. ↑ He, Jiuya; Mao, Chih-Chieh; Reyes, Aurelio; Sembongi, Hiroshi; Re, Miriam Di; Granycome, Caroline; Clippingdale, Andrew B.; Fearnley, Ian M.; Harbour, Michael (2007-01-15). "The AAA+ protein ATAD3 has displacement loop binding properties and is involved in mitochondrial nucleoid organization". The Journal of Cell Biology. 176 (2): 141–146. doi:10.1083/jcb.200609158. ISSN 0021-9525. PMC 2063933. PMID 17210950.
  9. ↑ Fish, Jennifer; Raule, Nicola; Attardi, Giuseppe (2004-12-17). "Discovery of a Major D-Loop Replication Origin Reveals Two Modes of Human mtDNA Synthesis" (PDF). Science. 306 (5704): 2098–2101. Bibcode:2004Sci...306.2098F. doi:10.1126/science.1102077. ISSN 0036-8075. PMID 15604407. S2CID 36033690.
  10. ↑ Burger; et al. (2003). "Unique mitochondrial genome architecture in unicellular relatives of animals". PNAS. 100 (3): 892–897. Bibcode:2003PNAS..100..892B. doi:10.1073/pnas.0336115100. PMC 298697. PMID 12552117.
  11. ↑ Fernández-García, J. L.; Carranza, J.; Martínez, J. G.; Randi, E. (2014-03-01). "Mitochondrial D-loop phylogeny signals two native Iberian red deer (Cervus elaphus) Lineages genetically different to Western and Eastern European red deer and infers human-mediated translocations". Biodiversity and Conservation. 23 (3): 537–554. doi:10.1007/s10531-013-0585-2. ISSN 0960-3115. S2CID 14719183.
  12. ↑ Silva; et al. (2016). "Genetic diversity analysis of major Sri Lankan goat populations using microsatellite and mitochondrial DNA D-loop variations". Small Ruminant Research. 148: 51–61. doi:10.1016/j.smallrumres.2016.12.030. hdl:11449/178557.
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