Vicent Guillermo P, Zaurin Roser, Ballaré Cecilia, Nacht A Silvina, Beato Miguel
Centre de Regulació Genòmica (CRG), Universitat Pompeu Fabra, Parc de Recerca Biomèdica (PRBB), Barcelona, Spain.
Nucl Recept Signal. 2009 Oct 2;7:e008. doi: 10.1621/nrs.07008.
Transcription from the mouse mammary tumor virus (MMTV) promoter can be induced by progestins. The progesterone receptor (PR) binds to a cluster of five hormone responsive elements (HREs) and activates the promoter by synergistic interactions with the ubiquitous transcription factor, nuclear factor 1 (NF1). Progesterone treatment of cells in culture leads to activation of the Src/Ras/Erk/Msk1 cascade. Selective inhibition of Erk, or its target kinase Msk1, interferes with chromatin remodeling and blocks MMTV activation. A complex of activated PR, Erk and Msk1 is recruited to promoter after 5 min of hormone treatment and phosphorylates histone H3 at serine 10. This modification promotes the displacement of HP1gamma and subsequent chromatin remodeling. Progestin treatment leads to the recruitment of the BAF complex, which selectively displaces histones H2A and H2B from the nucleosome containing the HREs. The acetyltransferase PCAF is also required for induction of progesterone target genes and acetylates histone H3 at K14, an epigenetic mark, which interacts with Brg1 and Brm, anchoring the BAF complex to chromatin. In nucleosomes assembled on either MMTV or mouse rDNA promoter sequences, SWI/SNF displaces histones H2A and H2B from MMTV, but not from the rDNA nucleosome. Thus, the outcome of nucleosome remodeling by purified SWI/SNF depends on DNA sequence. The resultant H3/H4 tetramer particle is then the substrate for subsequent events in induction. Thus, initial activation of the MMTV promoter requires activation of several kinases and PCAF leading to phosphoacetylation of H3, and recruitment of BAF with subsequent removal of H2A/H2B.
小鼠乳腺肿瘤病毒(MMTV)启动子的转录可被孕激素诱导。孕激素受体(PR)与五个激素反应元件(HREs)簇结合,并通过与普遍存在的转录因子核因子1(NF1)的协同相互作用激活启动子。在培养细胞中用孕激素处理会导致Src/Ras/Erk/Msk1级联反应的激活。对Erk或其靶激酶Msk1的选择性抑制会干扰染色质重塑并阻断MMTV的激活。激素处理5分钟后,活化的PR、Erk和Msk1复合物被募集到启动子上,并使组蛋白H3的丝氨酸10位点磷酸化。这种修饰促进了HP1γ的置换和随后的染色质重塑。孕激素处理导致BAF复合物的募集,该复合物选择性地从含有HREs的核小体中置换组蛋白H2A和H2B。乙酰转移酶PCAF对于孕激素靶基因的诱导也是必需的,并且在K14位点使组蛋白H3乙酰化,这是一种表观遗传标记,它与Brg1和Brm相互作用,将BAF复合物锚定到染色质上。在MMTV或小鼠rDNA启动子序列上组装的核小体中,SWI/SNF从MMTV中置换组蛋白H2A和H2B,但不从rDNA核小体中置换。因此,纯化的SWI/SNF进行核小体重塑的结果取决于DNA序列。由此产生的H3/H4四聚体颗粒随后成为诱导过程中后续事件的底物。因此,MMTV启动子的初始激活需要几种激酶和PCAF的激活,导致H3的磷酸乙酰化,并募集BAF,随后去除H2A/H2B。