Divergence towards a dead end? Cleavage of the divergent domains of ribosomal RNA in apoptosis.

Experientia Pub Date : 1996-10-31 DOI:10.1007/BF01920105
G Houge, S O Døskeland
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引用次数: 22

Abstract

In several cases of apoptotic death the large ribosomal subunit 28S rRNA is specifically cleaved. The cleavages appear at specific sites within those domains of the rRNA molecule that have shown exceptional high divergence in evolution (D domains). The cleavages accompany rather than precede apoptosis, and there is a positive, but not complete, correlation between rRNA cleavage and internucleosomal DNA fragmentation. Most cell types studied so far show two alternative cleavage pathways that are mutually exclusive. Cleavage can either start in the D8 domain with secondary cuts within a subdomain of D2 (D2c), or in the D2 domain with subsequent excision of the D2c subdomain. The latter pathway is of particular interest since D2 (unlike D8) is normally inaccessible for RNase attack. That apoptosis specifically affects the ribosomal divergent domains suggests that these domains, which make up roughly 25% of total cellular RNA, might have evolved to serve functions related to apoptosis. Future studies will be directed to test the hypothesis that rRNA fragmentation may be part of an apoptotic program directed against the elimination of illegitimate (viral?) polynucleotides.

分歧走向死胡同?细胞凋亡中核糖体RNA不同结构域的分裂。
在一些凋亡性死亡病例中,大核糖体亚基28S rRNA被特异性切割。这些切割出现在rRNA分子的特定位点上,这些区域在进化中表现出异常的高度分化(D区域)。切割伴随着细胞凋亡而不是先于细胞凋亡,rRNA切割与核小体间DNA断裂之间存在正相关,但不完全相关。迄今为止研究的大多数细胞类型都显示出两种互斥的分裂途径。切割可以从D8结构域开始,在D2的一个子结构域(D2c)内进行二次切割,或者在D2结构域开始,随后切除D2c子结构域。后一种途径是特别有趣的,因为D2(与D8不同)通常是RNase攻击无法进入的。细胞凋亡特别影响核糖体发散结构域,这表明这些结构域大约占细胞总RNA的25%,可能已经进化为与细胞凋亡相关的功能域。未来的研究将旨在验证rRNA断裂可能是针对消除非法(病毒?)多核苷酸的凋亡程序的一部分的假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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