TSBP1
Identifiers
AliasesTSBP1, TSBP, chromosome 6 open reading frame 10, testis expressed basic protein 1, C6orf10
External IDsOMIM: 618151 HomoloGene: 81753 GeneCards: TSBP1
Orthologs
SpeciesHumanMouse
Entrez

10665

n/a

Ensembl

n/a

UniProt

Q5SRN2

n/a

RefSeq (mRNA)

NM_001286474
NM_001286475
NM_006781

n/a

RefSeq (protein)

NP_001273403
NP_001273404
NP_006772

n/a

Location (UCSC)Chr 6: 32.29 – 32.37 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

TSBP1 is a protein that in humans is encoded by the TSBP1 gene.[3][4] C6orf10 is an open reading frame on chromosome 6 containing a protein that is ubiquitously expressed at low levels in the adult genome and may play a role during fetal development. C6orf10 has been found to be linked to both neurodegenerative and autoimmune diseases in adults. Expression of this gene is highest in the testis but is also seen in other tissue types such as the brain, lens of the eye and the medulla.[5][6][7] TSBP1 was previously known as C6orf10.

mRNA Transcript

Multiple sequence alignment of all C6orf10 human isoforms. This image was generated using Clustal W[8] and M view.[9]

C6orf10 contains seven human mRNA splice variants (a, b, c, X1, X2, X3, X4).

Conserved non-coding region

TSBP1 contains a highly conserved stem loop structure in the 3' UTR from bases 100–124.


Highly conserved stem loop structure from C6orf10 isoform a[10]

Protein

Composition

C6orf10 isoform a is rich in lysine (K), Glutamine (Q) and Glutamic acid (E) and poor in Histidine (H) and Phenylalanine(F)[11]]. Isoform a is a basic protein with an isoelectric point of 9 and a molecular weight of 62,000 kDa.[12]

This isoform contains two transmembrane regions near the beginning of the amino acid sequence.[13] The first transmembrane region spans from residue 6 to residue 25 (19 total residues) and has an isoelectric point of 5. The second transmembrane region spans from residue 100 to residue 119 (19 total residues) and has an isoelectric point of 8. Isoform a contains a PTZ00121 domain[14] starting with residue 221 and going until the end of the protein. There are several repetitive sequences within this domain.

Secondary Structure

TSBP1 consists mostly of alpha helices and random coils.[15] There are only a few regions that contain beta sheets.[16][17]

Subcellular Localization

TSBP1 is predicted to be localized to the Nucleus and the Endoplasmic Reticulum.[13] There is a signal peptide cleavage site between amino acid 30 and 31[18] which includes the first transmembrane domain. This N-terminal region of C6orf10 is likely localized to the endoplasmic reticulum. The C-terminal region of the protein contain two nuclear localization signals from amino acid 489-505 and 513-529 indicating that the section of the protein after the signal peptide cleavage site is localized to the nucleus.

Expression

TSBP1 is ubiquitously expressed at low levels in the adult human genome. In adults, expression of this gene is highest in the testis.[19] C6orf10 is expressed at higher levels in fetal and embryonic tissues. This indicates C6orf10 may play a role in development.

Tissue Expression profile of C6orf10 gene in preimplanted embryos
C6orf10 Tissue Expression Profile for adults. Orange dots indicate a very low level of expression while the blue bar indicates high expression.[19]

Regulation of expression

Transcriptional

TSBP1 has a promoter that is 1206 bases long.[20] This promoter overlaps with the 3' UTR but ends before the first codon. This promoter is fairly well conserved across primates except for a 136 nucleotide region midway through and the end of the promoter region.[21] Primates have insertions at these two regions that humans are missing. This may suggest that these regions of the promoter are not essential to humans.

Transcription factors

TSBP1 transcription is regulated by the binding of many transcription factors to the promoter region. The CCAAT binding protein and TATA box are highly conserved regions that are important in the initiation of transcription. Several of the transcription factors including EH1, NACA, NKX5-2, SIX4, VCR, etc. are involved in developmental pathways.[20]

Abbreviation Transcription Factor Full Name Matrix score Strand
CSRNP-1 Cytosine-Serine rich nuclear protein 1(AXUD1, AXIN1 up-regulated-1) 1.0 +
CCAAT Box CCAAT/enhancer binding protein (C/EBP), gamma 0.923 +
EH1 Engrailed Homeobox 1 0.862 +
Cart-1 Cartilage homeoprotein 1 0.997 -
ZFP 263 Zinc finger protein 263, ZKSCAN12 (Zinc finger protein with KRAB and SCAN domains 12) 0.921 +
SWI/SNF SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily, a member 3 0.999 -
TATA Box Vertebrate TATA binding protein factor 0.899 +
HSF2 Heat shock Factor 2 0.974 -
Hmx2/Nkx5-2 Hmx2/Nkx5-2 homeodomain transcription factor 0.933 +
Pdx1 Insulin promoter factor 1; pancreatic and duodenal homeobox 1 (Pdx1) 0.924 +
LMX1A LIM homeobox transcription factor 1 alpha 1.0 +
NACA Nascent polypeptide-associated complex subunit alpha 1 1.0 -
Oct1 Octamer binding factor 1 0.921 +
POU6F1 POU class 6 homeobox 1 0.973 +
STAT 5B Signal transducer and activator of transcription 5B 0.973 +
SIX 4 Sine oculis homeobox homolog 4 0.96 -
NMP4 Nuclear matrix protein 4 0.971 +
MSX Homeodomain proteins MSX-1 and MSX-2 0.989 -
AREB6 Atp1a1 regulatory element binding factor 6 1.0 -
VCR Vertebrate caudal related homeodomain protein 0.963 +

Protein Interactions

Most of the predicted protein interactions with C6orf10 are based solely on text mining and information gathered from genome-wide association studies. The two proteins with the highest interaction scores were Butyrophilin-like protein 2 (BTNL2) and Tetratricopeptide repeat domain containing TTC32.[22] BTNL2 is a negative regulator of T-cell activity and member of the immunoglobulin superfamily. BTNL2 is located in the C6orf10 gene neighborhood. TTC32 is from a protein family of structural repeat motifs that mediate protein-protein interactions in the formation of protein-protein complexes.[23] This may indicate the potential for C6orf10 to interact with another protein for form a complex.

Clinical significance

C6orf10 has been found to be associated with both neurodegenerative diseases and autoimmune diseases. These associations are mostly obtained from genome wide association studies. Common neurodegenerative diseases associated with C6orf10 include frontotemporal dementia, Parkinson's disease,[24] and Alzheimer's disease.[24] Autoimmune diseases associated with C6orf10 include Rheumatoid arthritis,[25][26][24][27] psoriasis,[28][27] multiple sclerosis,[29][24] Grave's disease[24] and lupus.

Homologs

Orthologs

By searching the NCBI BLAST database[30] for protein-protein interactions, it was found that C6orf10 is a protein only found in mammals. The BLAST database found the highest number of homologs in the Primates, Artiodactyla, and Carnivora. There were only a couple of homologs in the taxonomic orders of Rodentia, Chiroptera, and Perissodactyla. In the orders of Scandentia, Eulipotyphyla, Tubulidentata and sirenia there was only one complete homolog, but a few partial sequences do exist. There were partial protein sequences in Lagomorpha, Dermoptera, and Macroscelidea and there were no orthologs in Diprotodontia, Didelphimorphia, Cetacea, Dasyuromorphia, Pilosa, Monotremata, and Proboscidea. No homologs were found outside of mammals.

C6orf10 Isoform X4 Orthologs

Latin Name Common Name Identity Median Date of divergence (MYA)
Primates Homo sapiens Human 100% 0
Primates Gorilla gorilla gorilla Gorilla 83.36% 8.61
Primates Pongo abelii Sumatran Orangutan 82.81% 15.2
Carnivora Canis lupus familiaris Dog 49.79% 94
Carnivora Canis lupus dingo Australian Dog 49.33% 94
Artiodactyla Bubalus bubalis Water Buffalo 49.16% 94
Artiodactyla Equus caballus Horse 49.00% 94
Artiodactyla Odocoileus virginianus texanus White Tailed Deer 44.59% 94
Rodentia Chinchilla lanigera Chinchilla 41.99% 88
Rodentia Mus caroli Ryuku mouse 41.06% 88
Carnivora Felis catus Cat 40.77% 94
Rodentia Rattus norvegicus Brown Rat 37.45% 88

Paralogs

C6orf10 has one paralog that diverged about 135.6 million years ago. This paralog is called Thioredoxin domain containing protein 2 (TXNDC2).[30]

[1] BLAST: Basic Local Alignment Search Tool. National Center for Biotechnology InformationAvailable at: https://blast.ncbi.nlm.nih.gov/Blast.cgi. Accessdate 4 March 2019.

References

  1. 1 2 3 ENSG00000236672, ENSG00000204296, ENSG00000206310, ENSG00000234280, ENSG00000237881, ENSG00000232106, ENSG00000226892 GRCh38: Ensembl release 89: ENSG00000206245, ENSG00000236672, ENSG00000204296, ENSG00000206310, ENSG00000234280, ENSG00000237881, ENSG00000232106, ENSG00000226892 - Ensembl, May 2017
  2. ↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ↑ Stammers M, Rowen L, Rhodes D, Trowsdale J, Beck S (April 2000). "BTL-II: a polymorphic locus with homology to the butyrophilin gene family, located at the border of the major histocompatibility complex class II and class III regions in human and mouse". Immunogenetics. 51 (4–5): 373–82. doi:10.1007/s002510050633. PMID 10803852. S2CID 31938388.
  4. ↑ "Entrez Gene: C6orf10 chromosome 6 open reading frame 10".
  5. ↑ "AceView: Gene:C6orf10, a comprehensive annotation of human, mouse and worm genes with mRNAs or ESTsAceView". www.ncbi.nlm.nih.gov. Retrieved 25 February 2019.
  6. ↑ "TSBP1 testis expressed basic protein 1 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 25 February 2019.
  7. ↑ "Tissue expression of C6orf10 - Summary - The Human Protein Atlas". www.proteinatlas.org. Retrieved 25 February 2019.
  8. ↑ "Clustal Omega < Multiple Sequence Alignment < EMBL-EBI". www.ebi.ac.uk. Retrieved 6 May 2019.
  9. ↑ "MView < Multiple Sequence Alignment < EMBL-EBI". www.ebi.ac.uk. Retrieved 6 May 2019.
  10. ↑ "The Mfold Web Server | mfold.rit.albany.edu". unafold.rna.albany.edu. Retrieved 5 May 2019.
  11. ↑ "SAPS < Sequence Statistics < EMBL-EBI". www.ebi.ac.uk. Retrieved 6 May 2019.
  12. ↑ "ExPASy - Compute pI/Mw tool". web.expasy.org. Retrieved 6 May 2019.
  13. 1 2 "PSORT II Prediction". psort.hgc.jp. Retrieved 6 May 2019.
  14. ↑ "NCBI CDD CDD Conserved Protein Domain Neuromodulin_N". www.ncbi.nlm.nih.gov. Retrieved 6 May 2019.
  15. ↑ "Coils output". embnet.vital-it.ch. Retrieved 6 May 2019.
  16. ↑ "CFSSP: Chou & Fasman Secondary Structure Prediction Server". www.biogem.org. Retrieved 6 May 2019.
  17. ↑ "Archived". Archived from the original on 6 May 2019. Retrieved 30 May 2023.
  18. ↑ "ProP 1.0 Server - prediction results". www.cbs.dtu.dk. Retrieved 6 May 2019.
  19. 1 2 "TSBP1 testis expressed basic protein 1 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 6 May 2019.
  20. 1 2 "Genomatix - NGS Data Analysis & Personalized Medicine". www.genomatix.de. Retrieved 6 May 2019.
  21. ↑ "Human BLAT Search". genome.ucsc.edu. Retrieved 6 May 2019.
  22. ↑ "STRING: functional protein association networks". string-db.org. Retrieved 6 May 2019.
  23. ↑ Zeytuni N, Zarivach R (March 2012). "Structural and functional discussion of the tetra-trico-peptide repeat, a protein interaction module". Structure. 20 (3): 397–405. doi:10.1016/j.str.2012.01.006. PMID 22404999.
  24. 1 2 3 4 5 Zhang M, Ferrari R, Tartaglia MC, Keith J, Surace EI, Wolf U, et al. (October 2018). "A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers". Brain. 141 (10): 2895–2907. doi:10.1093/brain/awy238. PMC 6158742. PMID 30252044.
  25. ↑ Verma A, Basile AO, Bradford Y, Kuivaniemi H, Tromp G, Carey D, Gerhard GS, Crowe JE, Ritchie MD, Pendergrass SA (2016). "Phenome-Wide Association Study to Explore Relationships between Immune System Related Genetic Loci and Complex Traits and Diseases". PLOS ONE. 11 (8): e0160573. Bibcode:2016PLoSO..1160573V. doi:10.1371/journal.pone.0160573. PMC 4980020. PMID 27508393.
  26. ↑ Zheng W, Rao S (August 2015). "Knowledge-based analysis of genetic associations of rheumatoid arthritis to inform studies searching for pleiotropic genes: a literature review and network analysis". Arthritis Research & Therapy. 17 (1): 202. doi:10.1186/s13075-015-0715-1. PMC 4529690. PMID 26253105.
  27. 1 2 Malavia TA, Chaparala S, Wood J, Chowdari K, Prasad KM, McClain L, Jegga AG, Ganapathiraju MK, Nimgaonkar VL (2017). "Generating testable hypotheses for schizophrenia and rheumatoid arthritis pathogenesis by integrating epidemiological, genomic, and protein interaction data". npj Schizophrenia. 3: 11. doi:10.1038/s41537-017-0010-z. PMC 5441529. PMID 28560257.
  28. ↑ Feng BJ, Sun LD, Soltani-Arabshahi R, Bowcock AM, Nair RP, Stuart P, Elder JT, Schrodi SJ, Begovich AB, Abecasis GR, Zhang XJ, Callis-Duffin KP, Krueger GG, Goldgar DE (August 2009). "Multiple Loci within the major histocompatibility complex confer risk of psoriasis". PLOS Genetics. 5 (8): e1000606. doi:10.1371/journal.pgen.1000606. PMC 2718700. PMID 19680446.
  29. ↑ Lin X, Deng FY, Mo XB, Wu LF, Lei SF (January 2015). "Functional relevance for multiple sclerosis-associated genetic variants". Immunogenetics. 67 (1): 7–14. doi:10.1007/s00251-014-0803-4. PMID 25308886. S2CID 16113524.
  30. 1 2 "BLAST: Basic Local Alignment Search Tool". blast.ncbi.nlm.nih.gov. Retrieved 6 May 2019.

Further reading

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