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果蝇DOCK家族蛋白海绵在胸部发育过程中调节JNK信号通路。

Drosophila DOCK family protein sponge regulates the JNK pathway during thorax development.

作者信息

Morishita Kazushige, Ozasa Fumito, Eguchi Koichi, Yoshioka Yasuhide, Yoshida Hideki, Hiai Hiroshi, Yamaguchi Masamitsu

机构信息

Department of Applied Biology, Kyoto Institute of Technology.

出版信息

Cell Struct Funct. 2014;39(2):113-24. doi: 10.1247/csf.14008. Epub 2014 Oct 11.

Abstract

The dedicator of cytokinesis (DOCK) family proteins that are conserved in a wide variety of species are known as DOCK1-DOCK11 in mammals. The Sponge (Spg) is a Drosophila counterpart to the mammalian DOCK3. Specific knockdown of spg by pannir-GAL4 or apterous-GAL4 driver in wing discs induced split thorax phenotype in adults. Reduction of the Drosophila c-Jun N-terminal kinase (JNK), basket (bsk) gene dose enhanced the spg knockdown-induced phenotype. Conversely, overexpression of bsk suppressed the split thorax phenotype. Monitoring JNK activity in the wing imaginal discs by immunostaining with anti-phosphorylated JNK (anti-pJNK) antibody together with examination of lacZ expression in a puckered-lacZ enhancer trap line revealed the strong reduction of the JNK activity in the spg knockdown clones. This was further confirmed by Western immunoblot analysis of extracts from wing discs of spg knockdown fly with anti-pJNK antibody. Furthermore, the Duolink in situ Proximity Ligation Assay method detected interaction signals between Spg and Rac1 in the wing discs. Taken together, these results indicate Spg positively regulates JNK pathway that is required for thorax development and the regulation is mediated by interaction with Rac1.

摘要

在多种物种中保守的细胞分裂 dedicator(DOCK)家族蛋白在哺乳动物中被称为 DOCK1 - DOCK11。海绵体(Spg)是哺乳动物 DOCK3 在果蝇中的对应物。通过翼盘上的 pannir - GAL4 或无翅 - GAL4 驱动子特异性敲低 spg,会在成虫中诱导出胸部裂开的表型。果蝇 c - Jun N 末端激酶(JNK)、篮状蛋白(bsk)基因剂量的降低增强了 spg 敲低诱导的表型。相反,bsk 的过表达抑制了胸部裂开的表型。通过用抗磷酸化 JNK(抗 pJNK)抗体进行免疫染色并结合检查褶皱 - lacZ 增强子陷阱系中的 lacZ 表达来监测翼成虫盘中的 JNK 活性,结果显示在 spg 敲低克隆中 JNK 活性大幅降低。用抗 pJNK 抗体对 spg 敲低果蝇的翼盘提取物进行 Western 免疫印迹分析进一步证实了这一点。此外,Duolink 原位邻近连接分析方法检测到翼盘中 Spg 和 Rac1 之间的相互作用信号。综上所述,这些结果表明 Spg 正向调节胸部发育所需的 JNK 通路,并且这种调节是通过与 Rac1 的相互作用介导的。

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