POT1

POT1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
Aliases POT1, CMM10, HGLM9, protection of telomeres 1
External IDs MGI: 2141503 HomoloGene: 32263 GeneCards: POT1
Genetically Related Diseases
chronic lymphocytic leukemia[1]
RNA expression pattern


More reference expression data
Orthologs
Species Human Mouse
Entrez

25913

101185

Ensembl

ENSG00000128513

ENSMUSG00000029676

UniProt

Q9NUX5

Q91WC1

RefSeq (mRNA)

NM_001042594
NM_015450

NM_133931

RefSeq (protein)

NP_001036059.1
NP_056265.2
NP_001036059.1

NP_598692.1

Location (UCSC) Chr 7: 124.82 – 124.93 Mb Chr 6: 25.74 – 25.81 Mb
PubMed search [2] [3]
Wikidata
View/Edit HumanView/Edit Mouse

Protection of telomeres protein 1 is a protein that in humans is encoded by the POT1 gene.[4][5][6]

Function

This gene is a member of the telombin family and encodes a nuclear protein involved in telomere maintenance. Specifically, this protein functions as a member of a multi-protein complex known as shelterin, that binds to the TTAGGG repeats of telomeres, regulating telomere length and protecting chromosome ends from illegitimate recombination, catastrophic chromosome instability, and abnormal chromosome segregation. Alternatively spliced transcript variants have been described.[6]

Interactions

POT1 has been shown to interact with ACD[7][8][9] and TINF2.[8][9][10]

Pathology

References

  1. "Diseases that are genetically associated with POT1 view/edit references on wikidata".
  2. "Human PubMed Reference:".
  3. "Mouse PubMed Reference:".
  4. Baumann P, Cech TR (May 2001). "Pot1, the putative telomere end-binding protein in fission yeast and humans". Science. 292 (5519): 1171–5. doi:10.1126/science.1060036. PMID 11349150.
  5. Baumann P, Podell E, Cech TR (Oct 2002). "Human Pot1 (Protection of Telomeres) Protein: Cytolocalization, Gene Structure, and Alternative Splicing". Mol Cell Biol. 22 (22): 8079–87. doi:10.1128/MCB.22.22.8079-8087.2002. PMC 134737Freely accessible. PMID 12391173.
  6. 1 2 "Entrez Gene: POT1 POT1 protection of telomeres 1 homolog (S. pombe)".
  7. Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (Oct 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
  8. 1 2 Ye JZ, Hockemeyer D, Krutchinsky AN, Loayza D, Hooper SM, Chait BT, de Lange T (Jul 2004). "POT1-interacting protein PIP1: a telomere length regulator that recruits POT1 to the TIN2/TRF1 complex". Genes Dev. 18 (14): 1649–54. doi:10.1101/gad.1215404. PMC 478187Freely accessible. PMID 15231715.
  9. 1 2 Liu D, Safari A, O'Connor MS, Chan DW, Laegeler A, Qin J, Songyang Z (Jul 2004). "PTOP interacts with POT1 and regulates its localization to telomeres". Nat. Cell Biol. 6 (7): 673–80. doi:10.1038/ncb1142. PMID 15181449.
  10. Loayza D, De Lange T (Jun 2003). "POT1 as a terminal transducer of TRF1 telomere length control". Nature. 423 (6943): 1013–8. doi:10.1038/nature01688. PMID 12768206.
  11. Ramsay AJ, Quesada V, Foronda M, Conde L, Martínez-Trillos A, Villamor N, Rodríguez D, Kwarciak A, Garabaya C, Gallardo M, López-Guerra M, López-Guillermo A, Puente XS, Blasco MA, Campo E, López-Otín C (2013). "POT1 mutations cause telomere dysfunction in chronic lymphocytic leukemia". Nat. Genet. 45 (5): 526–30. doi:10.1038/ng.2584. PMID 23502782.
  12. Robles-Espinoza CD, Harland M, Ramsay AJ, Aoude LG, Quesada V, Ding Z, Pooley KA, Pritchard AL, Tiffen JC, Petljak M, Palmer JM, Symmons J, Johansson P, Stark MS, Gartside MG, Snowden H, Montgomery GW, Martin NG, Liu JZ, Choi J, Makowski M, Brown KM, Dunning AM, Keane TM, López-Otín C, Gruis NA, Hayward NK, Bishop DT, Newton-Bishop JA, Adams DJ (2014). "POT1 loss-of-function variants predispose to familial melanoma". Nat. Genet. 46 (5): 478–81. doi:10.1038/ng.2947. PMC 4266105Freely accessible. PMID 24686849.
  13. Bainbridge MN, Armstrong GN, Gramatges MM, Bertuch AA, Jhangiani SN, Doddapaneni H, Lewis L, Tombrello J, Tsavachidis S, Liu Y, Jalali A, Plon SE, Lau CC, Parsons DW, Claus EB, Barnholtz-Sloan J, Il'yasova D, Schildkraut J, Ali-Osman F, Sadetzki S, Johansen C, Houlston RS, Jenkins RB, Lachance D, Olson SH, Bernstein JL, Merrell RT, Wrensch MR, Walsh KM, Davis FG, Lai R, Shete S, Aldape K, Amos CI, Thompson PA, Muzny DM, Gibbs RA, Melin BS, Bondy ML (2015). "Germline mutations in shelterin complex genes are associated with familial glioma". J. Natl. Cancer Inst. 107 (1). doi:10.1093/jnci/dju384. PMID 25482530.

Further reading


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