生物
劈理(地质)
细胞生物学
抄写(语言学)
积分器
调节器
核糖核酸
生物发生
基因
分子生物学
遗传学
物理
古生物学
量子力学
断裂(地质)
哲学
语言学
电压
作者
Kevin Sabath,Chunhong Qiu,Stefanie Jonas
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2024-07-19
卷期号:84 (15): 2882-2899.e10
被引量:3
标识
DOI:10.1016/j.molcel.2024.06.032
摘要
The modular Integrator complex is a transcription regulator that is essential for embryonic development. It attenuates coding gene expression via premature transcription termination and performs 3'-processing of non-coding RNAs. For both activities, Integrator requires endonuclease activity that is harbored by an RNA cleavage module consisting of INTS4-9-11. How correct assembly of Integrator modules is achieved remains unknown. Here, we show that BRAT1 and WDR73 are critical biogenesis factors for the human cleavage module. They maintain INTS9-11 inactive during maturation by physically blocking the endonuclease active site and prevent premature INTS4 association. Furthermore, BRAT1 facilitates import of INTS9-11 into the nucleus, where it is joined by INTS4. Final BRAT1 release requires locking of the mature cleavage module conformation by inositol hexaphosphate (IP
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