Department of Biochemistry and Molecular Biology, University of Medicine and Dentistry of New Jersey, New Jersey Medical School, 185 South Orange Avenue, Newark, NJ 07103, USA.
FEBS Lett. 2012 Aug 14;586(17):2615-8. doi: 10.1016/j.febslet.2012.04.040. Epub 2012 May 2.
Since their discovery as cellular counterparts of viral oncogenes more than two decades ago, enormous progress has been made in unraveling the complex regulatory pathways of signal transduction initiated by the Crk family of proteins. New structural and biochemical studies have uncovered novel insights into both negative and positive regulation of Crk mediated by its atypical carboxyl-terminal SH3 domain (SH3C). Moreover, SH3C is tyrosine phosphorylated by receptor tyrosine kinases and non-receptor tyrosine kinases, thereby permitting assemblages of other SH2/PTB domain containing proteins. Such non-canonical signaling by the Crk SH3C reveals new regulatory strategies for adaptor proteins.
自二十多年前发现作为病毒癌基因的细胞对应物以来,人们在揭示 Crk 蛋白家族启动的信号转导的复杂调节途径方面取得了巨大进展。新的结构和生化研究揭示了 Crk 的非典型羧基末端 SH3 结构域 (SH3C) 对其介导的负调控和正调控的新见解。此外,Crk 的 SH3C 被受体酪氨酸激酶和非受体酪氨酸激酶磷酸化酪氨酸,从而允许其他含有 SH2/PTB 结构域的蛋白质组装。Crk SH3C 的这种非典型信号转导揭示了衔接蛋白的新调控策略。