PMS1

PMS1
사용 가능한 구조물
PDB	휴먼 유니프로트 검색: PDBe RCSB
PDB ID 코드 목록
	2CS1
식별자
별칭	PMS1, HNPCC3, PMSL1, hMLH2, PMS1 호몰로고 1, 수리 시스템 구성 요소 불일치
외부 ID	OMIM: 600258 MGI: 1202302 HomoloGene: 449 GeneCard: PMS1
유전자 위치(인간)
쳇.	염색체 2 (인간)
끝	189,877,629 bp
유전자 위치(마우스)
쳇.	1번 염색체(쥐)
끝	53,297,018 bp
RNA 표현 패턴
	표현된 상단
	고환; ; 콩팥을; ; 자궁내막; ; 폐를 끼치다; ; 뱃속; ; 하트; ; 아킬레스건;
	추가 참조 표현식 데이터
	추가 참조 표현식 데이터
유전자 온톨로지
분자함수	단일 가닥의 DNA 결합; DNA 결합; ATP 바인딩; 일치하지 않는 DNA 결합; ATPase 활동; 효소 결합;
셀룰러 컴포넌트	뮤틀알파 콤플렉스; 핵의; 불일치 수리 복합체;
생물학적 과정	DNA 수리; DNA 손상 자극에 대한 세포 반응; 수리 불일치;
	출처:아미고 / 퀵고
직교체
	5378
	227099
	ENSG00000064933
	ENSMUSG00000026098
	P54277; Q5FBZ4
	n/a
NM_000534; NM_001128143; NM_001128144; NM_001289408; NM_001289409;
	NM_001321044; NM_001321045; NM_001321046; NM_001321047; NM_001321048; NM_001321049; NM_001321051
	NM_153556
NP_000525; NP_001121615; NP_0011216; NP_001276337; NP_001276338;
	NP_001307973; NP_001307974; NP_001307975; NP_001307976; NP_001307977; NP_001307978; NP_001307980
	n/a
	위키다타
인간 보기/편집	마우스 보기/편집

PMS1 단백질 호몰로로그 1은 인간에서 PMS1 유전자에 의해 암호화된 단백질이다.^[5]^[6]

함수

이 유전자에 의해 암호화된 단백질은 DNA 불일치 수리에 관련된 효모 단백질에 대한 호몰로 확인되었다. 이 단백질의 불일치 수리에 대한 역할은 입증되지 않았다. 그러나 이 단백질은 DNA 불일치 치료 단백질인 MLH1과 헤테로디메이터를 형성하고 있으며, 일부 유전성 비폴리페스 대장암 사례에서 이 유전자에 돌연변이가 있는 것으로 밝혀졌다.^[6]

참조

^ ^a ^b ^c GRCh38: 앙상블 릴리스 89: ENSG000064933 - 앙상블, 2017년 5월
^ ^a ^b ^c GRCm38: 앙상블 릴리스 89: ENSMUSG000026098 - 앙상블, 2017년 5월
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Nicolaides NC, Papadopoulos N, Liu B, Wei YF, Carter KC, Ruben SM, Rosen CA, Haseltine WA, Fleischmann RD, Fraser CM (Sep 1994). "Mutations of two PMS homologues in hereditary nonpolyposis colon cancer". Nature. 371 (6492): 75–80. doi:10.1038/371075a0. PMID 8072530. S2CID 4244907.
^ ^a ^b "Entrez Gene: PMS1 PMS1 postmeiotic segregation increased 1 (S. cerevisiae)".

추가 읽기

Kolodner R (1996). "Biochemistry and genetics of eukaryotic mismatch repair". Genes Dev. 10 (12): 1433–42. doi:10.1101/gad.10.12.1433. PMID 8666228.
Horii A, Han HJ, Sasaki S, Shimada M, Nakamura Y (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.
Papadopoulos N, Nicolaides NC, Wei YF, Ruben SM, Carter KC, Rosen CA, Haseltine WA, Fleischmann RD, Fraser CM, Adams MD (1994). "Mutation of a mutL homolog in hereditary colon cancer". Science. 263 (5153): 1625–9. doi:10.1126/science.8128251. PMID 8128251.
Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
Yanagisawa Y, Ito E, Iwahashi Y, Akiyama Y, Yuasa Y, Maruyama K (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, Dengler H, Droese M, Berger H (1999). "Expression of DNA mismatch repair genes in naevi". In Vivo. 13 (3): 251–4. PMID 10459502.
Wang Q, Lasset C, Desseigne F, Saurin JC, Maugard C, Navarro C, Ruano E, Descos L, Trillet-Lenoir V, Bosset JF, Puisieux A (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. doi:10.1007/s004390051067. 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. doi:10.1159/000015546. PMID 10828585. S2CID 84779733.
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. doi:10.1093/nar/29.8.1695. PMC 31313. PMID 11292842.
Plotz G, Raedle J, Brieger A, Trojan J, Zeuzem S (2002). "hMutSα forms an ATP-dependent complex with hMutLα and hMutLβ on DNA". Nucleic Acids Res. 30 (3): 711–8. doi:10.1093/nar/30.3.711. PMC 100294. PMID 11809883.
Kotoula V, Hytiroglou P, Kaloutsi V, Barbanis S, Kouidou S, Papadimitriou CS (2003). "Mismatch repair gene expression in malignant lymphoproliferative disorders of B-cell origin". Leuk. Lymphoma. 43 (2): 393–9. doi:10.1080/10428190290006215. PMID 11999575. S2CID 19755282.
Plotz G, Raedle J, Brieger A, Trojan J, Zeuzem S (2003). "N-terminus of hMLH1 confers interaction of hMutLα and hMutLβ with hMutSα". Nucleic Acids Res. 31 (12): 3217–26. doi:10.1093/nar/gkg420. PMC 162253. 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. PMC 434232. PMID 15226443.
Okada T, Noji S, Goto Y, Iwata T, Fujita T, Okada T, Matsuzaki Y, Kuwana M, Hirakata M, Horii A, Matsuno S, Sunamura M, Kawakami Y (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. S2CID 880049.
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 (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.
Cannavo E, Gerrits B, Marra G, Schlapbach R, Jiricny J (2007). "Characterization of the interactome of the human MutL homologues MLH1, PMS1, and PMS2" (PDF). J. Biol. Chem. 282 (5): 2976–86. doi:10.1074/jbc.M609989200. PMID 17148452. S2CID 25279332.

인간 염색체 2의 유전자에 관한 이 기사는 단조롭다. 위키피디아를 확장하여 도울 수 있다.

[refGRCh38Ensembl-1] GRCh38: 앙상블 릴리스 89: ENSG000064933 - 앙상블, 2017년 5월

[refGRCm38Ensembl-2] GRCm38: 앙상블 릴리스 89: ENSMUSG000026098 - 앙상블, 2017년 5월

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid8072530-5] Nicolaides NC, Papadopoulos N, Liu B, Wei YF, Carter KC, Ruben SM, Rosen CA, Haseltine WA, Fleischmann RD, Fraser CM (Sep 1994). "Mutations of two PMS homologues in hereditary nonpolyposis colon cancer". Nature. 371 (6492): 75–80. doi:10.1038/371075a0. PMID 8072530. S2CID 4244907.

[entrez-6] "Entrez Gene: PMS1 PMS1 postmeiotic segregation increased 1 (S. cerevisiae)".

[1]

[2]

[3]

[4]

[5]

[6]

Search

PMS1

네임스페이스

더

함수

참조

추가 읽기