首页> 外文OA文献 >Analysis of Drosophila Cyclin EI and II function during development: Identification of an inhibitory zone within the morphogenetic furrow of the eye imaginal disc that blocks the function of Cyclin EI but not Cyclin EII
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Analysis of Drosophila Cyclin EI and II function during development: Identification of an inhibitory zone within the morphogenetic furrow of the eye imaginal disc that blocks the function of Cyclin EI but not Cyclin EII

机译:发育过程中果蝇Cyclin EI和II功能的分析:在成像细胞的形态发生沟中识别阻断细胞周期蛋白EI但不抑制细胞周期蛋白EII功能的抑制区

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摘要

The Drosophilacyclin E (DmcycE) gene gives rise to two transcripts encoding proteins that differ at their N termini, DmcycEII and DmcycEI. This study presents the first in vivo dissection of Cyclin E function. Ectopic expression studies using N- and C-terminal deletions of DmcycEI revealed that a region of 322 residues surrounding the cyclin box is sufficient to induce entry of G₁-arrested larval eye imaginal disc cells into S phase. Ectopic expression of DmcycEI in the eye disc has been previously shown to drive anterior, but not posterior, G₁-phase cells within the morphogenetic furrow (MF) into S phase. Significantly, ectopic expression of DmcycEII and N-terminal deletions of DmcycEI were able to drive all G₁ cells within the morphogenetic furrow into S phase, while a C-terminal deletion of DmcycEI could not. The p21 homolog Dacapo was shown by yeast two-hybrid, coimmunolocalization, and in vivo functional studies not to be the mediator of the DmcycEI inhibition in posterior part of the MF. Taken together, these results reveal a novel zone within the posterior region of the MF where DmcycEI but not DmcycEII function is inhibited, and suggest that DmcycEII is a more potent inducer of S phase.
机译:果蝇环素E(DmcycE)基因产生两个转录物,它们编码在其N末端不同的蛋白质,DmcycEII和DmcycEI。这项研究提出了Cyclin E功能的第一个体内解剖。使用DmcycEI的N-和C-末端缺失进行异位表达研究表明,细胞周期蛋白盒周围的322个残基区域足以诱导G-捕集的幼虫眼假想盘细胞进入S期。 DmcycEI在眼球盘中的异位表达已被证明可将形态发生犁沟(MF)内的前G₁期细胞驱动而不是后入G期细胞进入S期。值得注意的是,DmcycEII的异位表达和DmcycEI的N末端缺失能够将形态发生沟中的所有G₁细胞驱动到S期,而DmcycEI的C末端缺失则不能。酵母双杂交,共免疫定位和体内功能研究显示p21同源物Dacapo不是MF后部DmcycEI抑制的介体。综上所述,这些结果揭示了在MF的后部区域中的新区域,其中DmcycEI而不是DmcycEII功能被抑制,并且表明DmcycEII是S期的更有效的诱导剂。

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