Hirota Kouji, Mizuno Ken-ichi, Shibata Takehiko, Ohta Kunihiro
Shibata Distinguished Senior Scientist Laboratory, RIKEN Discovery Research Institute, Wako-shi, Saitama 351-0198, Japan.
Mol Biol Cell. 2008 Mar;19(3):1162-73. doi: 10.1091/mbc.e07-04-0377. Epub 2008 Jan 16.
Histone acetyltransferases (HATs) and ATP-dependent chromatin remodeling factors (ADCRs) regulate transcription and recombination via alteration of local chromatin configuration. The ade6-M26 allele of Schizosaccharomyces pombe creates a meiotic recombination hotspot that requires a cAMP-responsive element (CRE)-like sequence M26, the Atf1/Pcr1 heterodimeric ATF/CREB transcription factor, the Gcn5 HAT, and the Snf22 SWI2/SNF2 family ADCR. Chromatin alteration occurs meiotically around M26, leading to the activation of meiotic recombination. We newly report the roles of other chromatin remodeling factors that function positively and negatively in chromatin alteration at M26: two CHD-1 family ADCRs (Hrp1 and Hrp3), a Spt-Ada-Gcn5 acetyltransferase component (Ada2), and a member of Moz-Ybf2/Sas3-Sas2-Tip60 family (Mst2). Ada2, Mst2, and Hrp3 are required for the full activation of chromatin changes around M26 and meiotic recombination. Acetylation of histone H3 around M26 is remarkably reduced in gcn5Delta, ada2Delta and snf22Delta, suggesting cooperative functions of these HAT complexes and Snf22. Conversely, Hrp1, another CHD-1 family ADCR, maintains repressive chromatin configuration at ade6-M26. Interestingly, transcriptional initiation site is shifted to a site around M26 from the original initiation sites, in couple with the histone acetylation and meiotic chromatin alteration induced around 3' region of M26, suggesting a collaboration between these chromatin modulators and the transcriptional machinery to form accessible chromatin. These HATs and ADCRs are also required for the regulation of transcription and chromatin structure around M26 in response to osmotic stress. Thus, we propose that multiple chromatin modulators regulate chromatin structure reversibly and participate in the regulation of both meiotic recombination and stress-induced transcription around CRE-like sequences.
组蛋白乙酰转移酶(HATs)和ATP依赖的染色质重塑因子(ADCRs)通过改变局部染色质构型来调节转录和重组。粟酒裂殖酵母的ade6 - M26等位基因产生一个减数分裂重组热点,该热点需要一个cAMP反应元件(CRE)样序列M26、Atf1/Pcr1异二聚体ATF/CREB转录因子、Gcn5 HAT和Snf22 SWI2/SNF2家族ADCR。染色质改变在减数分裂时发生在M26周围,导致减数分裂重组的激活。我们首次报道了其他染色质重塑因子在M26处染色质改变中发挥正向和负向作用:两个CHD - 1家族ADCR(Hrp1和Hrp3)、一个Spt - Ada - Gcn5乙酰转移酶组分(Ada2)以及Moz - Ybf2/Sas3 - Sas2 - Tip60家族的一个成员(Mst2)。Ada2、Mst2和Hrp3是M26周围染色质变化和减数分裂重组完全激活所必需的。在gcn5Δ、ada2Δ和snf22Δ中,M26周围组蛋白H3的乙酰化显著降低,表明这些HAT复合物和Snf22具有协同功能。相反,另一个CHD - 1家族ADCR Hrp1在ade6 - M26处维持抑制性染色质构型。有趣的是,转录起始位点从原来的起始位点转移到了M26周围的一个位点,同时在M26的3'区域周围诱导了组蛋白乙酰化和减数分裂染色质改变,这表明这些染色质调节剂与转录机制之间存在协作以形成可及的染色质。这些HATs和ADCRs也是响应渗透胁迫调节M26周围转录和染色质结构所必需的。因此,我们提出多种染色质调节剂可逆地调节染色质结构,并参与CRE样序列周围减数分裂重组和应激诱导转录的调节。