Juranek Stefan A, Rupprecht Sina, Postberg Jan, Lipps Hans J
Institute of Cell Biology, University Witten/Herdecke, Stockumer Str. 10, D-58453 Witten, Germany.
Eukaryot Cell. 2005 Nov;4(11):1934-41. doi: 10.1128/EC.4.11.1934-1941.2005.
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.
在纤毛虫的大核发育过程中,存在几种针对微核特异性DNA序列进行特异性切除的模型。虽然模板引导的重组模型表明重组事件会导致在模板引导下对大核目的序列(MDS)进行特异性DNA切除和重新排序,但有证据表明,一种与RNA干扰相关的机制参与了全毛类纤毛虫的DNA消除过程。我们描述了在毛口目纤毛虫游仆虫中,与微核特异性序列同源的小核仁RNA(snRNA)在大核分化过程中合成。蛋白质免疫印迹和原位分析表明,组蛋白H3在大核分化过程中从头在赖氨酸9位点发生甲基化,染色质免疫沉淀显示微核特异性序列与甲基化的H3相关联。为了将这两个观察结果联系起来,RNA诱导沉默复合体成员PIWI同源物的表达被沉默。在这些细胞中,甲基化的微核特异性组蛋白H3变体“X”仍存在于大核原基中,且未观察到组蛋白H3的赖氨酸9甲基化。我们认为,snRNA会将染色质修饰酶招募到待切除的序列上。基于我们和早期的观察结果,我们认为这种机制不足以在发育中的大核中对序列进行特异性切除和MDS重新排序,并提出了一个关于毛口目纤毛虫内部消除序列切除和MDS重新排序的模型。