PRPF3

PRPF3
사용 가능한 구조물
PDB	직교 검색: PDBe RCSB
PDB ID 코드 목록
	1X4Q, 3JCR
식별자
별칭	PRPF3, 사전 mRNA 처리 인자 3, HPRP3, HPRP3P, PRP3, Prp3p, RP18, SNRNP90
외부 ID	OMIM: 607301 MGI: 1918017 호몰로진: 3447 GeneCard: PRPF3
유전자 위치(인간)
쳇.	염색체 1 (인간)
끝	150,353,233 bp
유전자 위치(마우스)
쳇.	3번 염색체(쥐)
끝	95,763,192 bp
RNA 표현 패턴
	표현된 상단
	수근신경; ; 갑상선; ; 뇌하수체;
	추가 참조 표현식 데이터
	추가 참조 표현식 데이터
유전자 온톨로지
분자함수	GO:0001948 단백질 결합; 동일한 단백질 결합; RNA 결합;
셀룰러 컴포넌트	카잘 보디; U4/U6 x U5 tri-snNP 복합체; 이음체 복합체; 핵의; 핵종의; 시토솔; 핵 반점; 단백질 함유 복합체; U2형 사전분석성 스플라이소솜;
생물학적 과정	트랜세스터화 반응을 통한 RNA 스플리싱; mRNA 스플라이싱, 스플라이소솜을 통해; mRNA처리; 스플라이소셜 트리-snNP 복합 어셈블리; RNA 스플라이싱;
	출처:아미고 / 퀵고
직교체
	9129
	70767
	ENSG00000117360
	ENSMUSG00000015748
	O4395
	Q922U1
	NM_004698; NM_001350529
	NM_027541; NM_001316751
	NP_004689; NP_001337458
	NP_001303680; NP_081817
	위키다타
인간 보기/편집	마우스 보기/편집

U4/U6 소형 핵 리보핵단백질 Prp3는 인간에서 PRPF3 유전자에 의해 암호화된 단백질이다.^[5]

함수

핵 프리 mRNA에서 인트론 제거는 4개의 작은 핵 리보뉴클레오프로틴(snRNP) 입자와 일시적으로 연관되지 않은 다수의 스플리싱 인자로 구성된 스플리소솜이라는 콤플렉스에서 발생한다.PRPF3는 U4 및 U6 snRNP와 관련된 여러 단백질 중 하나이다.[OMIM에 의해 제공]^[5]

상호작용

PRPF3는 DVL3와 상호작용하는 것으로 나타났다.^[6]

참조

^ ^a ^b ^c GRCh38: 앙상블 릴리스 89: ENSG00000117360 - 앙상블, 2017년 5월
^ ^a ^b ^c GRCm38: 앙상블 릴리스 89: ENSMUSG000015748 - 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.
^ ^a ^b "Entrez Gene: PRPF3 PRP3 pre-mRNA processing factor 3 homolog (S. cerevisiae)".
^ Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, et al. (Oct 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.

추가 읽기

Maruyama K, Sugano S (Jan 1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
Xu SY, Schwartz M, Rosenberg T, Gal A (Aug 1996). "A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentromeric region of chromosome 1". Human Molecular Genetics. 5 (8): 1193–7. doi:10.1093/hmg/5.8.1193. PMID 8842740.
Wang A, Forman-Kay J, Luo Y, Luo M, Chow YH, Plumb J, Friesen JD, Tsui LC, Heng HH, Woolford JL, Hu J (Nov 1997). "Identification and characterization of human genes encoding Hprp3p and Hprp4p, interacting components of the spliceosome". Human Molecular Genetics. 6 (12): 2117–26. doi:10.1093/hmg/6.12.2117. PMID 9328476.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (Oct 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
Horowitz DS, Kobayashi R, Krainer AR (Dec 1997). "A new cyclophilin and the human homologues of yeast Prp3 and Prp4 form a complex associated with U4/U6 snRNPs". RNA. 3 (12): 1374–87. PMC 1369579. PMID 9404889.
Heng HH, Wang A, Hu J (Mar 1998). "Mapping of the human HPRP3 and HPRP4 genes encoding U4/U6-associated splicing factors to chromosomes 1q21.1 and 9q31-q33". Genomics. 48 (2): 273–5. doi:10.1006/geno.1997.5181. PMID 9521884.
Xu SY, Rosenberg T, Gal A (Apr 1998). "Refined genetic mapping of autosomal dominant retinitis pigmentosa locus RP18 reduces the critical region to 2 cM between D1S442 and D1S2858 on chromosome 1q". Human Genetics. 102 (4): 493–4. doi:10.1007/s004390050728. PMID 9600251. S2CID 39815355.
Reidt U, Reuter K, Achsel T, Ingelfinger D, Lührmann R, Ficner R (Mar 2000). "Crystal structure of the human U4/U6 small nuclear ribonucleoprotein particle-specific SnuCyp-20, a nuclear cyclophilin" (PDF). The Journal of Biological Chemistry. 275 (11): 7439–42. doi:10.1074/jbc.275.11.7439. PMID 10713041. S2CID 20261807.
Chakarova CF, Hims MM, Bolz H, Abu-Safieh L, Patel RJ, Papaioannou MG, Inglehearn CF, Keen TJ, Willis C, Moore AT, Rosenberg T, Webster AR, Bird AC, Gal A, Hunt D, Vithana EN, Bhattacharya SS (Jan 2002). "Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa". Human Molecular Genetics. 11 (1): 87–92. doi:10.1093/hmg/11.1.87. PMID 11773002.
Horowitz DS, Lee EJ, Mabon SA, Misteli T (Feb 2002). "A cyclophilin functions in pre-mRNA splicing". The EMBO Journal. 21 (3): 470–80. doi:10.1093/emboj/21.3.470. PMC 125845. PMID 11823439.
Gonzalez-Santos JM, Wang A, Jones J, Ushida C, Liu J, Hu J (Jun 2002). "Central region of the human splicing factor Hprp3p interacts with Hprp4p". The Journal of Biological Chemistry. 277 (26): 23764–72. doi:10.1074/jbc.M111461200. PMID 11971898.
Nottrott S, Urlaub H, Lührmann R (Oct 2002). "Hierarchical, clustered protein interactions with U4/U6 snRNA: a biochemical role for U4/U6 proteins". The EMBO Journal. 21 (20): 5527–38. doi:10.1093/emboj/cdf544. PMC 129076. PMID 12374753.
Ajuh P, Chusainow J, Ryder U, Lamond AI (Dec 2002). "A novel function for human factor C1 (HCF-1), a host protein required for herpes simplex virus infection, in pre-mRNA splicing". The EMBO Journal. 21 (23): 6590–602. doi:10.1093/emboj/cdf652. PMC 136956. PMID 12456665.
Martínez-Gimeno M, Gamundi MJ, Hernan I, Maseras M, Millá E, Ayuso C, García-Sandoval B, Beneyto M, Vilela C, Baiget M, Antiñolo G, Carballo M (May 2003). "Mutations in the pre-mRNA splicing-factor genes PRPF3, PRPF8, and PRPF31 in Spanish families with autosomal dominant retinitis pigmentosa". Investigative Ophthalmology & Visual Science. 44 (5): 2171–7. doi:10.1167/iovs.02-0871. PMID 12714658.
Reidt U, Wahl MC, Fasshauer D, Horowitz DS, Lührmann R, Ficner R (Aug 2003). "Crystal structure of a complex between human spliceosomal cyclophilin H and a U4/U6 snRNP-60K peptide". Journal of Molecular Biology. 331 (1): 45–56. doi:10.1016/S0022-2836(03)00684-3. hdl:11858/00-001M-0000-0012-F238-B. PMID 12875835.
Wada Y, Itabashi T, Sato H, Tamai M (Nov 2004). "Clinical features of a Japanese family with autosomal dominant retinitis pigmentosa associated with a Thr494Met mutation in the HPRP3 gene". Graefe's Archive for Clinical and Experimental Ophthalmology = Albrecht von Graefes Archiv für Klinische und Experimentelle Ophthalmologie. 242 (11): 956–61. doi:10.1007/s00417-004-0923-x. PMID 15085354. S2CID 22773384.
Stanĕk D, Neugebauer KM (Sep 2004). "Detection of snRNP assembly intermediates in Cajal bodies by fluorescence resonance energy transfer". The Journal of Cell Biology. 166 (7): 1015–25. doi:10.1083/jcb.200405160. PMC 2172029. PMID 15452143.
Maita H, Kitaura H, Ariga H, Iguchi-Ariga SM (Jan 2005). "Association of PAP-1 and Prp3p, the products of causative genes of dominant retinitis pigmentosa, in the tri-snRNP complex". Experimental Cell Research. 302 (1): 61–8. doi:10.1016/j.yexcr.2004.08.022. PMID 15541726.

외부 링크

색소성 망막염 개요에 대한 GeneReviews/NIH/NCBI/UW 항목

인간 염색체 1번 유전자에 관한 이 기사는 단조롭다.위키피디아를 확장하여 도울 수 있다.

[refGRCh38Ensembl-1] GRCh38: 앙상블 릴리스 89: ENSG00000117360 - 앙상블, 2017년 5월

[refGRCm38Ensembl-2] GRCm38: 앙상블 릴리스 89: ENSMUSG000015748 - 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.

[entrez-5] "Entrez Gene: PRPF3 PRP3 pre-mRNA processing factor 3 homolog (S. cerevisiae)".

[pmid16189514-6] Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, et al. (Oct 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.

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PRPF3

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함수

상호작용

참조

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