Indian Institute of Science, Bangalore, India.
BMC Genomics. 2009 Dec 22;10:622. doi: 10.1186/1471-2164-10-622.
Protein kinases are involved in diverse spectrum of cellular processes. Availability of draft version of the human genomic data in the year 2001 enabled recognition of repertoire of protein kinases. However, over the years the human genomic data is being refined and the current release of human genomic data has helped us to recognize a larger repertoire of over 900 human protein kinases represented mainly by splice variants.
Many of these identified protein kinases are alternatively spliced products. Interestingly, some of the human kinase splice variants appear to be significantly diverged in terms of their functional properties as represented by incorporation or absence of one or more domains. Many sets of protein kinase splice variants have substantially different domain organization and in a few sets of splice variants kinase domains belong to different subfamilies of kinases suggesting potential participation in different signal transduction pathways.
Addition or deletion of a domain between splice variants of multi-domain kinases appears to be a means of generating differences in the functional features of otherwise similar kinases. It is intriguing that marked sequence diversity within the catalytic regions of some of the splice variant kinases result in kinases belonging to different subfamilies. These human kinase splice variants with different functions might contribute to diversity of eukaryotic cellular signaling.
蛋白激酶参与多种细胞过程。2001 年人类基因组数据草案的出现,使人们能够识别蛋白激酶的组成。然而,多年来,人类基因组数据不断得到完善,目前发布的人类基因组数据帮助我们识别了 900 多种主要由剪接变异体组成的人类蛋白激酶。
许多这些鉴定的蛋白激酶是选择性剪接的产物。有趣的是,一些人类激酶剪接变异体在功能特性上似乎有很大的差异,表现为一个或多个结构域的存在或缺失。许多蛋白激酶剪接变异体的结构域组织有很大的不同,在一些剪接变异体中,激酶结构域属于不同的激酶亚家族,表明它们可能参与不同的信号转导途径。
多结构域激酶的剪接变异体之间添加或缺失一个结构域似乎是产生功能特征差异的一种方式,而在一些剪接变异体激酶的催化区域内存在显著的序列多样性,导致它们属于不同的激酶亚家族,这令人着迷。这些具有不同功能的人类激酶剪接变异体可能有助于真核细胞信号的多样性。