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果蝇C端结合蛋白dCtBP是感觉器官前模式所必需的,并能增强GATA因子Pnr的原神经转录活性。

Drosophila C-terminal binding protein, dCtBP is required for sensory organ prepattern and sharpens proneural transcriptional activity of the GATA factor Pnr.

作者信息

Biryukova Inna, Heitzler Pascal

机构信息

Department of Developmental Biology, Institut de Génétique et de Biologie, Moléculaire et Cellulaire, Illkirch Cedex, BP 10142, France.

出版信息

Dev Biol. 2008 Nov 1;323(1):64-75. doi: 10.1016/j.ydbio.2008.08.014. Epub 2008 Aug 22.

Abstract

The peripheral nervous system is required for animals to detect and to relay environmental stimuli to central nervous system for the information processing. In Drosophila, the precise spatial and temporal expression of two proneural genes achaete (ac) and scute (sc), is necessary for development of the sensory organs. Here we present an evidence that the transcription co-repressor, dCtBP acts as a negative regulator of sensory organ prepattern. Loss of dCtBP function mutant exhibits ectopic sensory organs, while overexpression of dCtBP results in a dramatic loss of sensory organs. These phenotypes are correlated with mis-emerging of sensory organ precursors and perturbated expression of proneural transcription activator Ac. Mammalian CtBP-1 was identified via interaction with the consensus motif PXDLSX(K/R) of adenovirus E1A oncoprotein. We demonstrated that dCtBP binds directly to PLDLS motif of Drosophila Friend of GATA-1 protein, U-shaped and sharpens the adult sensory organ development. Moreover, we found that dCtBP mediates multivalent interaction with the GATA transcriptional activator Pannier and acts as a direct co-repressor of the Pannier-mediated activation of proneural genes. We demonstrated that Pannier genetically interacts with dCtBP-interacting protein HDAC1, suggesting that the dCtBP-dependent regulation of Pannier activity could utilize a repressive mechanism involving alteration of local chromatine structure.

摘要

动物需要外周神经系统来检测环境刺激并将其传递给中枢神经系统进行信息处理。在果蝇中,两个原神经基因achaete(ac)和scute(sc)精确的时空表达对于感觉器官的发育是必需的。在此,我们提供证据表明转录共抑制因子dCtBP作为感觉器官前模式的负调节因子。dCtBP功能缺失突变体表现出异位感觉器官,而dCtBP的过表达导致感觉器官显著缺失。这些表型与感觉器官前体的错误出现以及原神经转录激活因子Ac的表达紊乱相关。哺乳动物CtBP-1是通过与腺病毒E1A癌蛋白的共有基序PXDLSX(K/R)相互作用而被鉴定出来的。我们证明dCtBP直接与果蝇GATA-1蛋白的Friend、U-shaped的PLDLS基序结合,并使成虫感觉器官发育更加精确。此外,我们发现dCtBP介导与GATA转录激活因子Pannier的多价相互作用,并作为Pannier介导的原神经基因激活的直接共抑制因子。我们证明Pannier与dCtBP相互作用蛋白HDAC1存在遗传相互作用,这表明dCtBP依赖的Pannier活性调节可能利用了一种涉及局部染色质结构改变的抑制机制。

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