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Src激酶激活与功能的部分见解。

Selected glimpses into the activation and function of Src kinase.

作者信息

Bjorge J D, Jakymiw A, Fujita D J

机构信息

Cancer Biology Research Group, Department of Biochemistry and Molecular Biology, University of Calgary Medical Center, 3330 Hospital Dr. N.W., Calgary, Alberta T2N 4N1, Canada.

出版信息

Oncogene. 2000 Nov 20;19(49):5620-35. doi: 10.1038/sj.onc.1203923.

Abstract

Since the discovery of the v-src and c-src genes and their products, much progress has been made in the elucidation of the structure, regulation, localization, and function of the Src protein. Src is a non-receptor protein tyrosine kinase that transduces signals that are involved in the control of a variety of cellular processes such as proliferation, differentiation, motility, and adhesion. Src is normally maintained in an inactive state, but can be activated transiently during cellular events such as mitosis, or constitutively by abnormal events such as mutation (i.e. v-Src and some human cancers). Activation of Src occurs as a result of disruption of the negative regulatory processes that normally suppress Src activity, and understanding the various mechanisms behind Src activation has been a target of intense study. Src associates with cellular membranes, in particular the plasma membrane, and endosomal membranes. Studies indicate that the different subcellular localizations of Src could be important for the regulation of specific cellular processes such as mitogenesis, cytoskeletal organization, and/or membrane trafficking. This review will discuss the history behind the discovery and initial characterization of Src and the regulatory mechanisms of Src activation, in particular, regulation by modification of the carboxy-terminal regulatory tyrosine by phosphatases and kinases. Its focus will then turn to the different subcellular localizations of Src and the possible roles of nuclear and perinuclear targets of Src. Finally, a brief section will review some of our present knowledge regarding Src involvement in human cancers.

摘要

自从发现v-src和c-src基因及其产物以来,在阐明Src蛋白的结构、调控、定位和功能方面已经取得了很大进展。Src是一种非受体蛋白酪氨酸激酶,它转导参与多种细胞过程控制的信号,如增殖、分化、运动和黏附。Src通常保持无活性状态,但在有丝分裂等细胞事件期间可被短暂激活,或因突变等异常事件(即v-Src和某些人类癌症)而持续激活。Src的激活是由于通常抑制Src活性的负调控过程被破坏所致,了解Src激活背后的各种机制一直是深入研究的目标。Src与细胞膜相关,特别是质膜和内体膜。研究表明,Src不同的亚细胞定位对于有丝分裂、细胞骨架组织和/或膜运输等特定细胞过程的调控可能很重要。本综述将讨论Src发现和初步表征背后的历史以及Src激活的调控机制,特别是通过磷酸酶和激酶对羧基末端调控酪氨酸的修饰进行的调控。然后其重点将转向Src不同的亚细胞定位以及Src核内和核周靶点的可能作用。最后,简短部分将综述我们目前关于Src参与人类癌症的一些知识。

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