Aronica Lucia, Bednenko Janna, Noto Tomoko, DeSouza Leroi V, Siu K W Michael, Loidl Josef, Pearlman Ronald E, Gorovsky Martin A, Mochizuki Kazufumi
Institute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna, Austria.
Genes Dev. 2008 Aug 15;22(16):2228-41. doi: 10.1101/gad.481908.
Tetrahymena eliminates micronuclear-limited sequences from the developing macronucleus during sexual reproduction. Homology between the sequences to be eliminated and approximately 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.
四膜虫在有性生殖过程中会从发育中的大核中消除微核限制序列。待消除序列与一种与AGO蛋白家族蛋白Twi1p相关的约28个核苷酸的小RNA(scnRNAs)之间的同源性可能是这一消除过程的基础。然而,Twi1p - scnRNA复合物识别微核限制序列的机制尚不清楚。我们发现,一种与Twi1p相关的假定RNA解旋酶Ema1p是Twi1p与染色质相互作用所必需的。这一需求解释了EMA1基因敲除菌株的表型,包括与大核注定序列同源的scnRNAs选择性下调的丧失、发育中的新大核中H3K9和K27甲基化的丧失以及DNA消除失败。我们进一步证明,Twi1p与来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减少。我们提出,Ema1p通过刺激亲代和发育中的新大核中scnRNAs与非编码转录本之间的碱基配对相互作用来发挥DNA消除功能。