Central European Institute of Technology (CEITEC), Masaryk University, Brno, Czech Republic.
The Francis Crick Institute, London, UK.
Nat Struct Mol Biol. 2020 May;27(5):500-510. doi: 10.1038/s41594-020-0406-8. Epub 2020 May 4.
Replication-dependent histones (RDH) are required for packaging of newly synthetized DNA into nucleosomes during the S phase when their expression is highly upregulated. However, the mechanisms of this upregulation in metazoan cells remain poorly understood. Using iCLIP and ChIP-seq, we found that human cyclin-dependent kinase 11 (CDK11) associates with RNA and chromatin of RDH genes primarily in the S phase. Moreover, its amino-terminal region binds FLASH, an RDH-specific 3'-end processing factor, which keeps the kinase on the chromatin. CDK11 phosphorylates serine 2 (Ser2) of the carboxy-terminal domain of RNA polymerase II (RNAPII), which is initiated when RNAPII reaches the middle of RDH genes and is required for further RNAPII elongation and 3'-end processing. CDK11 depletion leads to decreased number of cells in S phase, likely owing to the function of CDK11 in RDH gene expression. Thus, the reliance of RDH expression on CDK11 could explain why CDK11 is essential for the growth of many cancers.
复制依赖性组蛋白(RDH)在 S 期时高度上调,在该时期,它们将新合成的 DNA 包装到核小体中。然而,真核细胞中这种上调的机制仍知之甚少。通过 iCLIP 和 ChIP-seq,我们发现人类周期蛋白依赖性激酶 11(CDK11)主要在 S 期与 RDH 基因的 RNA 和染色质结合。此外,其氨基末端区域与 FLASH 结合,FLASH 是一种 RDH 特异性的 3'末端加工因子,它使激酶保持在染色质上。CDK11 磷酸化 RNA 聚合酶 II(RNAPII)羧基末端结构域的丝氨酸 2(Ser2),当 RNAPII 到达 RDH 基因的中间时,该磷酸化就开始发生,并且是进一步的 RNAPII 延伸和 3'末端加工所必需的。CDK11 的耗竭导致 S 期细胞数量减少,这可能归因于 CDK11 在 RDH 基因表达中的功能。因此,RDH 表达对 CDK11 的依赖可以解释为什么 CDK11 对许多癌症的生长至关重要。