Department of Radiation Oncology, University of Utah School of Medicine, Salt Lake City, Utah 84112, USA.
Huntsman Cancer Institute, University of Utah School of Medicine, Salt Lake City, Utah 84112, USA.
Nat Commun. 2016 Jun 21;7:11949. doi: 10.1038/ncomms11949.
Histone H3K4 methylation is connected to gene transcription from yeast to humans, but its mechanistic roles in transcription and chromatin dynamics remain poorly understood. We investigated the functions for Set1 and Jhd2, the sole H3K4 methyltransferase and H3K4 demethylase, respectively, in S. cerevisiae. Here, we show that Set1 and Jhd2 predominantly co-regulate genome-wide transcription. We find combined activities of Set1 and Jhd2 via H3K4 methylation contribute to positive or negative transcriptional regulation. Providing mechanistic insights, our data reveal that Set1 and Jhd2 together control nucleosomal turnover and occupancy during transcriptional co-regulation. Moreover, we find a genome-wide co-regulation of chromatin structure by Set1 and Jhd2 at different groups of transcriptionally active or inactive genes and at different regions within yeast genes. Overall, our study puts forth a model wherein combined actions of Set1 and Jhd2 via modulating H3K4 methylation-demethylation together control chromatin dynamics during various facets of transcriptional regulation.
组蛋白 H3K4 甲基化与从酵母到人类的基因转录有关,但它在转录和染色质动力学中的机制作用仍知之甚少。我们研究了 Set1 和 Jhd2 的功能,它们分别是唯一的 H3K4 甲基转移酶和 H3K4 去甲基化酶,在 S. cerevisiae 中。在这里,我们表明 Set1 和 Jhd2 主要共同调节全基因组转录。我们发现 Set1 和 Jhd2 的联合活性通过 H3K4 甲基化有助于正或负转录调控。提供机制见解,我们的数据表明 Set1 和 Jhd2 共同控制转录共调控期间核小体周转和占据。此外,我们发现 Set1 和 Jhd2 在不同转录活跃或不活跃基因的不同组和酵母基因内的不同区域对染色质结构进行全基因组共同调控。总的来说,我们的研究提出了一个模型,其中 Set1 和 Jhd2 通过调节 H3K4 甲基化-去甲基化的联合作用共同控制转录调节的各个方面的染色质动力学。