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Histone Chaperones Nap1 and Vps75 Regulate Histone Acetylation during Transcription Elongation

机译:组蛋白伴侣Nap1和Vps75调节转录延伸过程中组蛋白乙酰化。

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Histone chaperones function in chromatin assembly and disassembly, suggesting they have important regulatory roles in transcription elongation. The Saccharomyces cerevisiae proteins Nap1 and Vps75 are structurally related, evolutionarily conserved histone chaperones. We showed that Nap1 genetically interacts with several transcription elongation factors and that both Nap1 and Vps75 interact with the RNA polymerase II kinase, CTK1. Loss of NAP1 or VPS75 suppressed cryptic transcription within the open reading frame (ORF) observed when strains are deleted for the kinase CTK1. Loss of the histone acetyltransferase Rtt109 also suppressed ctk1-dependent cryptic transcription. Vps75 regulates Rtt109 function, suggesting that they function together in this process. Histone H3 K9 was found to be the important lysine that is acetylated by Rtt109 during ctk1-dependent cryptic transcription. We showed that both Vps75 and Nap1 regulate the relative level of H3 K9 acetylation in the STE11 ORF. This supports a model in which Nap1, like Vps75, directly regulates Rtt109 activity or regulates the assembly of acetylated chromatin. Although Nap1 and Vps75 share many similarities, due to their distinct interactions with SET2, Nap1 and Vps75 may also play separate roles during transcription elongation. This work sheds further light on the importance of histone chaperones as general regulators of transcription elongation.
机译:组蛋白伴侣在染色质组装和拆卸中起作用,表明它们在转录延伸中具有重要的调节作用。酿酒酵母蛋白Nap1和Vps75是与结构相关的,进化上保守的组蛋白伴侣。我们发现Nap1在遗传上与几个转录延伸因子相互作用,并且Nap1和Vps75都与RNA聚合酶II激酶 CTK1 相互作用。当缺失激酶 CTK1 的菌株时, NAP1 VPS75 的丢失抑制了开放阅读框(ORF)内的隐性转录。组蛋白乙酰转移酶Rtt109的丢失也抑制了 ctk1 依赖的隐性转录。 Vps75调节Rtt109功能,表明它们在此过程中一起起作用。发现组蛋白H3 K9是重要的赖氨酸,在 ctk1 依赖的隐性转录过程中被Rtt109乙酰化。我们发现Vps75和Nap1均调节 STE11 ORF中H3 K9乙酰化的相对水平。这支持了其中Nap1像Vps75一样直接调节Rtt109活性或调节乙酰化染色质组装的模型。尽管Nap1和Vps75具有许多相似之处,但是由于它们与 SET2 的独特相互作用,Nap1和Vps75在转录延伸过程中也可能起着不同的作用。这项工作进一步阐明了组蛋白伴侣作为转录延伸的一般调节剂的重要性。

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