Suppr超能文献

RNA聚合酶II羧基末端结构域(CTD)的磷酸化调控

Regulated phosphorylation of the RNA polymerase II C-terminal domain (CTD).

作者信息

Bensaude O, Bonnet F, Cassé C, Dubois M F, Nguyen V T, Palancade B

机构信息

Laboratoire de génétique moléculaire, Ecole normale supérieure, Paris, France.

出版信息

Biochem Cell Biol. 1999;77(4):249-55.

Abstract

The largest subunit of RNA polymerase II has an intriguing feature in its carboxyl-terminal domain (CTD) that consists of multiple repeats of an evolutionary conserved motif of seven amino acids. CTD phosphorylation plays a pivotal role in controlling mRNA synthesis and maturation. In exponentially growing cells, the phosphate turnover on the CTD is fast; it is blocked by common inhibitors of transcription, such as 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole and actinomycin D. Transcription-independent changes in CTD phosphorylation are observed at critical developmental stages, such as meiosis and early development.

摘要

RNA聚合酶II的最大亚基在其羧基末端结构域(CTD)具有一个有趣的特征,该结构域由一个七氨基酸进化保守基序的多个重复序列组成。CTD磷酸化在控制mRNA合成和成熟过程中起关键作用。在指数生长的细胞中,CTD上的磷酸周转很快;它被转录的常见抑制剂如5,6-二氯-1-β-D-呋喃核糖基苯并咪唑和放线菌素D所阻断。在关键的发育阶段,如减数分裂和早期发育过程中,可观察到CTD磷酸化的转录非依赖性变化。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验