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光感受器细胞分化需要对转录抑制因子Tramtrack进行调控性蛋白水解。

Photoreceptor cell differentiation requires regulated proteolysis of the transcriptional repressor Tramtrack.

作者信息

Li S, Li Y, Carthew R W, Lai Z C

机构信息

Department of Biological Sciences, University of Pittsburgh, Pennsylvania 15260, USA.

出版信息

Cell. 1997 Aug 8;90(3):469-78. doi: 10.1016/s0092-8674(00)80507-3.

Abstract

The transcription repressor Tramtrack (TTK) is found in cone cells but not photoreceptor cells of the Drosophila eye. We show that down-regulation of TTK expression occurs in photoreceptor cells and is required for their fate determination. Down-regulation requires the presence of Phyllopod (PHYL), which is induced by the RAS pathway, and Seven In Absentia (SINA). Loss of either gene causes accumulation of TTK in photoreceptor cells, and TTK does not accumulate in cone cells if both PHYL and SINA are present. We report that SINA and PHYL promote ubiquitination and rapid degradation of TTK by the proteasome pathway in cell culture, and both SINA and PHYL bind to the N-terminal domain of TTK. These results argue that photoreceptor differentiation is regulated by the RAS pathway through targeted proteolysis of the TTK repressor.

摘要

转录抑制因子Tramtrack(TTK)存在于果蝇眼睛的视锥细胞中,但不存在于光感受器细胞中。我们发现,TTK表达的下调发生在光感受器细胞中,并且是其命运决定所必需的。下调需要由RAS途径诱导的叶足蛋白(PHYL)和无七蛋白(SINA)的存在。任何一个基因的缺失都会导致TTK在光感受器细胞中积累,如果同时存在PHYL和SINA,TTK则不会在视锥细胞中积累。我们报告称,在细胞培养中,SINA和PHYL通过蛋白酶体途径促进TTK的泛素化和快速降解,并且SINA和PHYL都与TTK的N端结构域结合。这些结果表明,光感受器的分化是由RAS途径通过对TTK抑制因子的靶向蛋白水解来调节的。

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