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染色质重塑因子CHD8与延伸中的RNA聚合酶II相互作用,并调控细胞周期蛋白E2基因的表达。

The chromatin remodeling factor CHD8 interacts with elongating RNA polymerase II and controls expression of the cyclin E2 gene.

作者信息

Rodríguez-Paredes M, Ceballos-Chávez M, Esteller M, García-Domínguez M, Reyes J C

机构信息

Centro Andaluz de Biología Molecular y Medicina Regenerativa (CABIMER), CSIC, Américo Vespucio s/n, E-41092 Sevilla, Spain.

出版信息

Nucleic Acids Res. 2009 May;37(8):2449-60. doi: 10.1093/nar/gkp101. Epub 2009 Mar 2.

DOI:10.1093/nar/gkp101
PMID:19255092
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2677868/
Abstract

CHD8 is a chromatin remodeling ATPase of the SNF2 family. We found that depletion of CHD8 impairs cell proliferation. In order to identify CHD8 target genes, we performed a transcriptomic analysis of CHD8-depleted cells, finding out that CHD8 controls the expression of cyclin E2 (CCNE2) and thymidylate synthetase (TYMS), two genes expressed in the G1/S transition of the cell cycle. CHD8 was also able to co-activate the CCNE2 promoter in transient transfection experiments. Chromatin immunoprecipitation experiments demonstrated that CHD8 binds directly to the 5' region of both CCNE2 and TYMS genes. Interestingly, both RNA polymerase II (RNAPII) and CHD8 bind constitutively to the 5' promoter-proximal region of CCNE2, regardless of the cell-cycle phase and, therefore, of the expression of CCNE2. The tandem chromodomains of CHD8 bind in vitro specifically to histone H3 di-methylated at lysine 4. However, CHD8 depletion does not affect the methylation levels of this residue. We also show that CHD8 associates with the elongating form of RNAPII, which is phosphorylated in its carboxy-terminal domain (CTD). Furthermore, CHD8-depleted cells are hypersensitive to drugs that inhibit RNAPII phosphorylation at serine 2, suggesting that CHD8 is required for an early step of the RNAPII transcription cycle.

摘要

CHD8是SNF2家族的一种染色质重塑ATP酶。我们发现CHD8的缺失会损害细胞增殖。为了鉴定CHD8的靶基因,我们对CHD8缺失的细胞进行了转录组分析,发现CHD8控制细胞周期蛋白E2(CCNE2)和胸苷酸合成酶(TYMS)的表达,这两个基因在细胞周期的G1/S转换期表达。在瞬时转染实验中,CHD8也能够共激活CCNE2启动子。染色质免疫沉淀实验表明,CHD8直接结合CCNE2和TYMS基因的5'区域。有趣的是,无论细胞周期阶段如何,因此无论CCNE2的表达如何,RNA聚合酶II(RNAPII)和CHD8都组成性地结合到CCNE2的5'启动子近端区域。CHD8的串联色域在体外特异性结合赖氨酸4二甲基化的组蛋白H3。然而,CHD8的缺失并不影响该残基的甲基化水平。我们还表明,CHD8与RNAPII的延伸形式相关,该延伸形式在其羧基末端结构域(CTD)中被磷酸化。此外,CHD8缺失的细胞对抑制丝氨酸2处RNAPII磷酸化的药物高度敏感,这表明CHD8是RNAPII转录周期早期步骤所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa73/2677868/9f416e48c26b/gkp101f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa73/2677868/2c0bb173fbfe/gkp101f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa73/2677868/c7a8776169be/gkp101f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa73/2677868/47e8d1606d16/gkp101f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa73/2677868/029f963fb5aa/gkp101f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa73/2677868/75b3c8c7d37a/gkp101f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa73/2677868/9f416e48c26b/gkp101f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa73/2677868/2c0bb173fbfe/gkp101f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa73/2677868/c7a8776169be/gkp101f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa73/2677868/47e8d1606d16/gkp101f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa73/2677868/029f963fb5aa/gkp101f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa73/2677868/75b3c8c7d37a/gkp101f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa73/2677868/9f416e48c26b/gkp101f6.jpg

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