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Study of an RNA helicase implicates small RNA–noncoding RNA interactions in programmed DNA elimination in Tetrahymena

机译:RNA解旋酶的研究牵扯到四膜虫在计划的DNA消除中的小RNA非编码RNA相互作用。

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摘要

Tetrahymena eliminates micronuclear-limited sequences from the developing macronucleus during sexual reproduction. Homology between the sequences to be eliminated and ∼28-nucleotide small RNAs (scnRNAs) associated with an Argonaute family protein Twi1p likely underlies this elimination process. However, the mechanism by which Twi1p–scnRNA complexes identify micronuclear-limited sequences is not well understood. We show that a Twi1p-associated putative RNA helicase Ema1p is required for the interaction between Twi1p and chromatin. This requirement explains the phenotypes of EMA1 KO strains, including loss of selective down-regulation of scnRNAs homologous to macronuclear-destined sequences, loss of H3K9 and K27 methylation in the developing new macronucleus, and failure to eliminate DNA. We further demonstrate that Twi1p interacts with noncoding transcripts derived from parental and developing macronuclei and this interaction is greatly reduced in the absence of Ema1p. We propose that Ema1p functions in DNA elimination by stimulating base-pairing interactions between scnRNAs and noncoding transcripts in both parental and developing new macronuclei.
机译:在有性生殖过程中,四膜虫从发育中的大核消除了微核限制的序列。要消除的序列与与Argonaute家族蛋白Twi1p相关的〜28个核苷酸的小RNA(scnRNA)之间的同源性很可能是这一消除过程的基础。但是,关于Twi1p–scnRNA复合物识别微核限制序列的机制尚不清楚。我们显示,Twi1p和染色质之间的相互作用需要Twi1p相关推定的RNA解旋酶Ema1p。该要求解释了EMA1 KO菌株的表型,包括与大核定序同源的scnRNA选择性下调的丧失,正在发育的新大核中H3K9和K27甲基化的丧失,以及无法消除DNA的现象。我们进一步证明,Twi1p与衍生自亲代和发育中的大核的非编码转录本相互作用,并且在没有Ema1p的情况下这种相互作用大大降低。我们提出,Ema1p在DNA消除中的功能是通过刺激亲本和正在发育的新大核中scnRNA和非编码转录本之间的碱基配对相互作用。

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