AKT2
AKT2RAC-베타세린/스레오닌-단백질 키나아제라고도 알려진 AKT2는 인간에서 AKT2 유전자에 의해 암호화된 효소다.[5][6]인슐린 신호 전달 경로의 일부로서 대사물 저장에 영향을 미친다.[5]
함수
이 유전자는 SH2 유사(Src homology 2-like) 도메인을 포함하는 세린/트레오닌 키나제스의 AKT 하위 계열에 속하는 단백질을 인코딩하는 putive onceneine이다.암호화된 단백질은 알려진 여러 단백질을 인산화할 수 있는 일반적인 단백질 키나아제다.[7]
AKT2는 인슐린 신호 전달 경로의 일부로 글리코제네시스, 글루코네제네시스,[5] 포도당 전달을 제어하는 데 중요한 역할을 한다.
임상적 유의성
이 유전자는 8개의 난소암 세포 라인 중 2개와 15개의 1차 난소 종양 중 2개에서 증폭되고 과다압박되는 것으로 나타났다.과도한 압박은 인간 덕트 췌장암의 일부분에서 발생하는 악성 표현 유형의 원인이 된다.[7]
Akt2가 부족한 생쥐는 정상적인 체질량이지만 심오한 당뇨 표현형을 보여, Akt2가 인슐린 수용체 하류의 신호 전달에 핵심적인 역할을 하고 있음을 알 수 있다.Akt2가 부족한 생쥐는 큰 T항원뿐만 아니라 신경 종양에 의해 시작된 유방암에서 더 나쁜 결과를 보여준다.[8]
상호작용
AKT2는 다음과 상호 작용하는 것으로 나타났다.
참조
- ^ a b c GRCh38: 앙상블 릴리스 89: ENSG00000105221 - 앙상블, 2017년 5월
- ^ a b c GRCm38: 앙상블 릴리스 89: ENSMUSG00000004056 - 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 c Tsoukas, Michael A.; Mantzoros, Christos S. (2016-01-01), Jameson, J. Larry; De Groot, Leslie J; de Kretser, David M.; Giudice, Linda C. (eds.), "Chapter 37 - Lipodystrophy Syndromes", Endocrinology: Adult and Pediatric (Seventh Edition), Philadelphia: W.B. Saunders, pp. 648–661.e5, doi:10.1016/b978-0-323-18907-1.00037-8, ISBN 978-0-323-18907-1, retrieved 2020-12-18
- ^ Cheng JQ, Godwin AK, Bellacosa A, Taguchi T, Franke TF, Hamilton TC, Tsichlis PN, Testa JR (November 1992). "AKT2, a putative oncogene encoding a member of a subfamily of protein-serine/threonine kinases, is amplified in human ovarian carcinomas". Proc Natl Acad Sci U S A. 89 (19): 9267–71. doi:10.1073/pnas.89.19.9267. PMC 50107. PMID 1409633.
- ^ a b "Entrez Gene: AKT2 v-akt murine thymoma viral oncogene homolog 2".
- ^ Heron-Milhavet L, Khouya N, Fernandez A, Lamb NJ (2011). "Akt1 and Akt2: differentiating the aktion". Histol. Histopathol. 26 (5): 651–62. PMID 21432781.
- ^ Mitsuuchi Y, Johnson SW, Sonoda G, Tanno S, Golemis EA, Testa JR (September 1999). "Identification of a chromosome 3p14.3-21.1 gene, APPL, encoding an adaptor molecule that interacts with the oncoprotein-serine/threonine kinase AKT2". Oncogene. 18 (35): 4891–8. doi:10.1038/sj.onc.1203080. PMID 10490823.
- ^ Yuan ZQ, Feldman RI, Sun M, Olashaw NE, Coppola D, Sussman GE, Shelley SA, Nicosia SV, Cheng JQ (August 2002). "Inhibition of JNK by cellular stress- and tumor necrosis factor alpha-induced AKT2 through activation of the NF kappa B pathway in human epithelial Cells". J. Biol. Chem. 277 (33): 29973–82. doi:10.1074/jbc.M203636200. PMID 12048203.
- ^ Figueroa C, Tarras S, Taylor J, Vojtek AB (November 2003). "Akt2 negatively regulates assembly of the POSH-MLK-JNK signaling complex". J. Biol. Chem. 278 (48): 47922–7. doi:10.1074/jbc.M307357200. PMID 14504284.
- ^ Laine J, Künstle G, Obata T, Noguchi M (February 2002). "Differential regulation of Akt kinase isoforms by the members of the TCL1 oncogene family". J. Biol. Chem. 277 (5): 3743–51. doi:10.1074/jbc.M107069200. PMID 11707444.
- ^ Laine J, Künstle G, Obata T, Sha M, Noguchi M (August 2000). "The protooncogene TCL1 is an Akt kinase coactivator". Mol. Cell. 6 (2): 395–407. doi:10.1016/S1097-2765(00)00039-3. PMID 10983986.
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