Kim Mijin, Kim Tae-Hee, Lee Hae-Hyeog
Department of Interdisciplinary Program in Biomedical Science, Soonchunhyang University, Asan, Korea.
Department of Obstetrics and Gynecology, Soonchunhyang University College of Medicine, Bucheon, Korea.
J Menopausal Med. 2016 Apr;22(1):6-8. doi: 10.6118/jmm.2016.22.1.6. Epub 2016 Apr 26.
The Jun activation-domain binding protein 1 (Jab1) recognize a potential coactivator of activator protein 1 (AP-1) such as c-fos, c-jun transcription factor and the fifth subunit of the COP9 signalosome complex. Also, Jab1 activate the c-jun gene resulted cell proliferation. Not only a powerful tumor suppressor but also regulator of apoptosis negative cdk inhibitor p27(kip1) are involved in the cell cycle. This is Jab1 and p27(kip1) interact with each other, Jab1 accelerate p27(kip1) from nuclear to cytoplasm through ubiquitin/proteasome pathway. However, information about the relationship between Jab1 and p27(kip1) is not known much. Taken together, the results of this study identify function and structure of Jab1 and p27(kip1) were described in a recent article on the basis of relevant. Besides Jab1 and p27(kip1) will organize the relationship between the disease and women.
Jun激活域结合蛋白1(Jab1)可识别激活蛋白1(AP-1)的潜在共激活因子,如c-fos、c-jun转录因子以及COP9信号体复合物的第五亚基。此外,Jab1激活c-jun基因导致细胞增殖。不仅强大的肿瘤抑制因子而且细胞周期负性调控因子凋亡抑制因子p27(kip1)也参与细胞周期。这是因为Jab1与p27(kip1)相互作用,Jab1通过泛素/蛋白酶体途径加速p27(kip1)从细胞核转运至细胞质。然而,关于Jab1与p27(kip1)之间关系的信息知之甚少。综上所述,本研究结果确定了Jab1和p27(kip1)的功能和结构,最近一篇相关文章对此进行了描述。此外,Jab1和p27(kip1)将梳理疾病与女性之间的关系。