Suppr超能文献

人细胞周期蛋白A保守细胞周期蛋白框内的序列足以与cdc2激酶结合并激活该激酶。

Sequences within the conserved cyclin box of human cyclin A are sufficient for binding to and activation of cdc2 kinase.

作者信息

Lees E M, Harlow E

机构信息

Massachusetts General Hospital Cancer Center, Charlestown 02129.

出版信息

Mol Cell Biol. 1993 Feb;13(2):1194-201. doi: 10.1128/mcb.13.2.1194-1201.1993.

Abstract

Cyclins are pivotal in the coordinate regulation of the cell cycle. By physical association, they are able to activate at least one of the cyclin-dependent kinases, cdc2. How this association between the catalytic moiety and cyclins leads to subsequent activation of the kinase remains unclear. In this report, we describe experiments to investigate this event at a physical level. Our approach was to map the regions required on the cyclin A molecule for interaction with cdc2. We have mapped the contact regions to two small noncontiguous stretches of amino acids, residues 189 to 241 and 275 to 320, both located within the conserved cyclin box domain of the protein. We have further shown that this region not only represents a contact site for cdc2 but apparently represents an intact functional domain with respect to cdc2 activation. This region alone is sufficient to stimulate maturation when injected into immature Xenopus laevis oocytes. This observation implies that events leading to the activation of cdc2 kinase can be mediated through small regions of the cyclin molecule that are located in the cyclin box. These regions contain some of the most highly conserved residues found between all the cyclin members so far identified. This suggests that the cyclin family members may have conserved a similar mechanism to bind and activate cyclin-dependent kinases.

摘要

细胞周期蛋白在细胞周期的协调调控中起着关键作用。通过物理结合,它们能够激活至少一种细胞周期蛋白依赖性激酶,即cdc2。催化部分与细胞周期蛋白之间的这种结合如何导致激酶随后的激活仍不清楚。在本报告中,我们描述了在物理层面研究这一事件的实验。我们的方法是绘制细胞周期蛋白A分子上与cdc2相互作用所需的区域。我们已将接触区域定位到两个不连续的小氨基酸片段,即第189至241位残基和第275至320位残基,它们都位于该蛋白保守的细胞周期蛋白框结构域内。我们进一步表明,该区域不仅代表cdc2的接触位点,而且就cdc2激活而言显然代表一个完整的功能结构域。当注入未成熟的非洲爪蟾卵母细胞时,仅该区域就足以刺激成熟。这一观察结果表明,导致cdc2激酶激活的事件可以通过位于细胞周期蛋白框内的细胞周期蛋白分子的小区域介导。这些区域包含了迄今为止在所有已鉴定的细胞周期蛋白成员之间发现的一些高度保守的残基。这表明细胞周期蛋白家族成员可能保留了一种类似的结合和激活细胞周期蛋白依赖性激酶的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/041d/359004/28933c668ea9/molcellb00014-0480-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验