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首页> 外文期刊>Eukaryotic cell >snRNA and Heterochromatin Formation Are Involved in DNA Excision during Macronuclear Development in Stichotrichous Ciliates
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snRNA and Heterochromatin Formation Are Involved in DNA Excision during Macronuclear Development in Stichotrichous Ciliates

机译:snRNA和异染色质形成参与在Stichotrichous纤毛虫的大核发育过程中的DNA切除。

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Several models for specific excision of micronucleus-specific DNA sequences during macronuclear development in ciliates exist. While the template-guided recombination model suggests recombination events resulting in specific DNA excision and reordering of macronucleus-destined sequences (MDS) guided by a template, there is evidence that an RNA interference-related mechanism is involved in DNA elimination in holotrichous ciliates. We describe that in the stichotrichous ciliate Stylonychia, snRNAs homologous to micronucleus-specific sequences are synthesized during macronuclear differentiation. Western and in situ analyses demonstrate that histone H3 becomes methylated at K9 de novo during macronuclear differentiation, and chromatin immunoprecipitation revealed that micronucleus-specific sequences are associated with methylated H3. To link both observations, expression of a PIWI homolog, member of the RNA-induced silencing complex, was silenced. In these cells, the methylated micronucleus-specific histone H3 variant “X” is still present in macronuclear anlagen and no K9 methylation of histone H3 is observed. We suggest that snRNA recruits chromatin-modifying enzymes to sequences to be excised. Based on our and earlier observations, we believe that this mechanism is not sufficient for specific excision of sequences and reordering of MDS in the developing macronucleus and propose a model for internal eliminated sequence excision and MDS reordering in stichotrichous ciliates.
机译:存在几种在纤毛虫的大核发育过程中特异性切除微核特异性DNA序列的模型。尽管模板指导的重组模型表明重组事件导致特定的DNA切除和模板指导的大核定序(MDS)的重新排序,但有证据表明,RNA干扰相关的机制参与了全纤毛纤毛DNA的消除。我们描述了在纤毛纤毛虫 Stylonychia 中,在大核分化过程中合成了与微核特异序列同源的snRNA。 Western和原位分析表明,组蛋白H3在大核分化过程中在K9从头甲基化,染色质免疫沉淀显示微核特异性序列与甲基化H3相关。为了将两个观察结果联系起来,沉默了RNA诱导的沉默复合体成员PIWI同源物的表达。在这些细胞中,甲基化的微核特异性组蛋白H3变体“ X”仍存在于大核胶原中,并且未观察到组蛋白H3的K9甲基化。我们建议snRNA募集染色质修饰酶来切除序列。根据我们和较早的观察,我们认为该机制不足以对发育中的大核中的序列进行特定的切除和MDS的重新排序,并为粘毛纤毛虫的内部消除的序列切除和MDS的重新排序提供了模型。

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