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The PWWP2A Histone Deacetylase Complex Represses Intragenic Spurious Transcription Initiation in mESCs

机译:PWWP2A组蛋白脱乙酰酶复合物抑制了MESCS中的腺体杂散转录

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摘要

Transcriptional fidelity depends on accurate promoter selection and initiation from the correct sites. In yeast, H3K36me3-mediated recruitment of the Rpd3S HDAC complex to gene bodies suppresses spurious transcription initiation. Here we describe an equivalent pathway in metazoans. PWWP2A/B is an H3K36me3 reader that forms a stable complex with HDAC1/2. We used CAGE-seq to profile all transcription initiation sites in wild-type mESCs and cells lacking PWWP2A/B. Loss of PWWP2A/B enhances spurious initiation from intragenic sites present in wild-type mESCs, and this effect is associated with increased levels of initiating Pol-II and histone acetylation. Spurious initiation events in Pwwp2a/b DKO mESCs do not overlap in genomic location or chromatin features with spurious sites that arise in Dnmt3b KO mESCs, previously reported to function in the suppression of intragenic transcriptional initiation, suggesting these pathways function cooperatively in maintaining the fidelity of transcription initiation in metazoans.
机译:转录保真度取决于准确的启动子选择和从正确部位开始。在酵母中,H3K36ME3介导的RPD3S HDAC复合物对基因体的募集抑制了杂散的转录起始。在这里,我们描述了美唑烷的等同途径。 PWWP2A / B是H3K36ME3读卡器,其与HDAC1 / 2形成稳定的复合物。我们使用笼式SEQ进行野生型MESC的所有转录起始位点和缺乏PWWP2A / B的细胞。 PWWP2A / B的丧失增强了野生型MESC中存在的腺体位点的寄生发育,并且这种效果与引发POL-II和组蛋白乙酰化的水平增加有关。 PWWP2A / B DKO MESCS中的杂散启动事件在基因组位置或染色质特征中不重叠,其在DNMT3B KO MESCS中出现的杂散部位,以前据报道抑制腺体转录启动,表明这些途径函数在保持保真度美唑烷转录启动。

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