Suppr超能文献

后期促进复合体

The anaphase promoting complex.

作者信息

Page A M, Hieter P

机构信息

Department of Molecular Biology and Genetics, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.

出版信息

Cancer Surv. 1997;29:133-50.

PMID:9338100
Abstract

We have proposed a preliminary model of how the anaphase promoting complex functions throughout the cell cycle, but despite the flurry of recent publications characterizing the APC--its components, regulation and substrate specificity--many fundamental questions remain to be answered. Firstly, the remaining components of the APC need to be identified and characterized. We do not know if all cyclosome components are conserved in all eukaryotes, or if higher eukaryotes, having a more complicated cell cycle machinery, maintain additional subunits for more sophisticated functional and regulatory control. In addition, we need to determine the identity of the various kinases and phosphatases that regulate the APC itself. The biochemistry of individual APC components is also a mystery, and a specific biochemical function has not been assigned to any known members of the complex. It is not at all clear which subunit(s) of the complex actually recognizes the E2 enzyme and which subunit(s) recognizes the cyclin destruction box. It is likely that many cyclosome substrates remain to be identified, and it will be interesting to determine whether all cyclosome substrates require a destruction box for their degradation or whether the APC recognizes other determinants of protein instability. Finally, we assume that the APC degrades mitotic cyclins in all proliferating cells, but whether it degrades unique cell cycle related substrates in specific tissues is unclear. Furthermore, nothing is known about APC function during meiosis, or whether the APC degrades other substrates that are not related to the cell cycle. This is an exciting and rapidly developing field in the exciting world of cell cycle biology. We expect that new findings will surely reveal many interesting surprises about this essential protein complex.

摘要

我们已经提出了一个关于后期促进复合体在整个细胞周期中如何发挥作用的初步模型,但是尽管最近有大量关于后期促进复合体(APC)的研究发表,包括其组成成分、调控机制和底物特异性等方面,但许多基本问题仍有待解答。首先,需要鉴定和表征后期促进复合体的其余组成成分。我们不知道所有的细胞周期体成分在所有真核生物中是否都保守,或者具有更复杂细胞周期机制的高等真核生物是否为了更精细的功能和调控控制而保留了额外的亚基。此外,我们需要确定调节后期促进复合体本身的各种激酶和磷酸酶的身份。单个后期促进复合体成分的生物化学性质也是一个谜,并且尚未为该复合体的任何已知成员赋予特定的生化功能。完全不清楚该复合体的哪些亚基实际上识别E2酶,哪些亚基识别细胞周期蛋白破坏框。很可能还有许多细胞周期体底物有待鉴定,确定所有细胞周期体底物的降解是否都需要破坏框,或者后期促进复合体是否识别蛋白质不稳定性的其他决定因素将会很有趣。最后,我们假设后期促进复合体在所有增殖细胞中降解有丝分裂细胞周期蛋白,但它是否在特定组织中降解独特的细胞周期相关底物尚不清楚。此外,关于后期促进复合体在减数分裂期间的功能,或者它是否降解与细胞周期无关的其他底物,我们一无所知。在令人兴奋的细胞周期生物学领域,这是一个令人兴奋且发展迅速的领域。我们预计新的发现肯定会揭示关于这个重要蛋白质复合体的许多有趣惊喜。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验