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Internal ribosome entry segment-mediated translation during apoptosis: the role of IRES-trans-acting factors.

机译:内部核糖体进入片段介导的细胞凋亡过程中的翻译:IRES反式作用因子的作用。

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摘要

During apoptosis, there is a reduction in translation initiation caused by caspase cleavage of several of the factors required for the cap-dependent scanning mechanism. Under these circumstances, many proteins that are required for apoptosis are instead translated by the alternative method of internal ribosome entry. This mechanism requires the formation of a complex RNA structural element and in the presence of internal ribosome entry segment (IRES)-trans-acting factors (ITAFs), the ribosome is recruited to the RNA. The interactions of several ITAFs with IRESs have been investigated in detail, and several mechanisms of action have been noted, including acting as chaperones, stabilising and remodelling the RNA structure. Structural remodelling by PTB in particular will be discussed, and how this protein is able to facilitate recruitment of the ribosome to several IRESs by causing previously occluded sites to become more accessible.Cell Death and Differentiation (2005) 12, 585-591. doi:10.1038/sj.cdd.4401642.
机译:在凋亡过程中,由半胱天冬酶裂解引起的依赖于帽的扫描机制所需的几种因素导致翻译起始的减少。在这种情况下,细胞凋亡所需的许多蛋白质反而通过内部核糖体进入的替代方法进行翻译。该机制需要形成复杂的RNA结构元件,并且在存在内部核糖体进入片段(IRES)反式作用因子(ITAF)的情况下,核糖体会被募集到RNA中。已经详细研究了几种ITAF与IRES的相互作用,并注意到了几种作用机理,包括充当分子伴侣,稳定和重塑RNA结构。特别是将讨论PTB的结构重塑,以及该蛋白如何通过使先前被阻塞的位点变得更易接近而促进核糖体向多个IRES的募集。CellDeath and Differentiation(2005)12,585-591。 doi:10.1038 / sj.cdd.4401642。

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