PMS1

From Wikipedia, the free encyclopedia

PMS1 postmeiotic segregation increased 1 (S. cerevisiae)

PDB rendering based on 2cs1.

Available structures: 2cs1

Identifiers

Symbol(s)

PMS1; DKFZp781M0253; HNPCC3; PMSL1; hPMS1

External IDs

OMIM: 600258 MGI: 1202302 HomoloGene: 449

Gene ontology
Molecular Function:	• nucleotide binding • DNA binding • ATP binding • GTP binding
Cellular Component:	• nucleus
Biological Process:	• mismatch repair • regulation of transcription, DNA-dependent • cell cycle • negative regulation of progression through cell cycle

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

n/a

Refseq

NM_000534 (mRNA)
NP_000525 (protein)

NM_153556 (mRNA)
NP_705784 (protein)

Location

Chr 2: 190.36 - 190.45 Mb

Chr 1: 53.13 - 53.24 Mb

Pubmed search

[1]

[2]

PMS1 postmeiotic segregation increased 1 (S. cerevisiae), also known as PMS1, is a human gene.^[1]

The protein encoded by this gene was identified by its homology to a yeast protein involved in DNA mismatch repair. A role for this protein in mismatch repair has not been proven. However, the protein forms heterodimers with MLH1, a DNA mismatch repair protein, and some cases of hereditary nonpolyposis colorectal cancer have been found to have mutations in this gene.^[1]

[edit] References

^ ^a ^b Entrez Gene: PMS1 PMS1 postmeiotic segregation increased 1 (S. cerevisiae).

[edit] Further reading

Kolodner R (1996). "Biochemistry and genetics of eukaryotic mismatch repair.". Genes Dev. 10 (12): 1433–42. PMID 8666228.
Horii A, Han HJ, Sasaki S, et al. (1994). "Cloning, characterization and chromosomal assignment of the human genes homologous to yeast PMS1, a member of mismatch repair genes.". Biochem. Biophys. Res. Commun. 204 (3): 1257–64. doi:10.1006/bbrc.1994.2598. PMID 7980603.
Nicolaides NC, Papadopoulos N, Liu B, et al. (1994). "Mutations of two PMS homologues in hereditary nonpolyposis colon cancer.". Nature 371 (6492): 75–80. doi:10.1038/371075a0. PMID 8072530.
Papadopoulos N, Nicolaides NC, Wei YF, et al. (1994). "Mutation of a mutL homolog in hereditary colon cancer.". Science 263 (5153): 1625–9. PMID 8128251.
Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery.". Genome Res. 6 (9): 791–806. PMID 8889548.
Yanagisawa Y, Ito E, Iwahashi Y, et al. (1998). "Isolation and characterization of the 5' region of the human mismatch repair gene hPMS1.". Biochem. Biophys. Res. Commun. 243 (3): 738–43. doi:10.1006/bbrc.1998.8165. PMID 9500994.
Korabiowska M, Brinck U, Ruschenburg I, et al. (1999). "Expression of DNA mismatch repair genes in naevi.". In Vivo 13 (3): 251–4. PMID 10459502.
Wang Q, Lasset C, Desseigne F, et al. (1999). "Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer.". Hum. Genet. 105 (1-2): 79–85. PMID 10480359.
Matton N, Simonetti J, Williams K (2000). "Identification of mismatch repair protein complexes in HeLa nuclear extracts and their interaction with heteroduplex DNA.". J. Biol. Chem. 275 (23): 17808–13. doi:10.1074/jbc.M909794199. PMID 10748159.
Alvarez Soria MA, Justesen J, Hansen LL (2000). "Assignment of the human postmeiotic segregation increased (S. cerevisiae) 1 (PMS1) to chromosome 2q31.1 by radiation hybrid mapping.". Cytogenet. Cell Genet. 88 (3-4): 200–1. PMID 10828585.
Kondo E, Horii A, Fukushige S (2001). "The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2.". Nucleic Acids Res. 29 (8): 1695–702. PMID 11292842.
Plotz G, Raedle J, Brieger A, et al. (2002). "hMutSalpha forms an ATP-dependent complex with hMutLalpha and hMutLbeta on DNA.". Nucleic Acids Res. 30 (3): 711–8. PMID 11809883.
Kotoula V, Hytiroglou P, Kaloutsi V, et al. (2003). "Mismatch repair gene expression in malignant lymphoproliferative disorders of B-cell origin.". Leuk. Lymphoma 43 (2): 393–9. PMID 11999575.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.
Plotz G, Raedle J, Brieger A, et al. (2003). "N-terminus of hMLH1 confers interaction of hMutLalpha and hMutLbeta with hMutSalpha.". Nucleic Acids Res. 31 (12): 3217–26. PMID 12799449.
Luo Y, Lin FT, Lin WC (2004). "ATM-mediated stabilization of hMutL DNA mismatch repair proteins augments p53 activation during DNA damage.". Mol. Cell. Biol. 24 (14): 6430–44. doi:10.1128/MCB.24.14.6430-6444.2004. PMID 15226443.
Okada T, Noji S, Goto Y, et al. (2005). "Immune responses to DNA mismatch repair enzymes hMSH2 and hPMS1 in patients with pancreatic cancer, dermatomyositis and polymyositis.". Int. J. Cancer 116 (6): 925–33. doi:10.1002/ijc.21118. PMID 15856462.
Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network.". Nature 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
Cannavo E, Gerrits B, Marra G, et al. (2007). "Characterization of the interactome of the human MutL homologues MLH1, PMS1, and PMS2.". J. Biol. Chem. 282 (5): 2976–86. doi:10.1074/jbc.M609989200. PMID 17148452.