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RNF12/RLIM E3 泛素连接酶对染色质的靶向作用控制转录反应。

Chromatin targeting of the RNF12/RLIM E3 ubiquitin ligase controls transcriptional responses.

机构信息

https://ror.org/01zg1tt02 MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, UK.

https://ror.org/018906e22 Department of Developmental Biology, Erasmus University Medical Center, Rotterdam, Netherlands.

出版信息

Life Sci Alliance. 2024 Jan 10;7(3). doi: 10.26508/lsa.202302282. Print 2024 Mar.

Abstract

Protein ubiquitylation regulates key biological processes including transcription. This is exemplified by the E3 ubiquitin ligase RNF12/RLIM, which controls developmental gene expression by ubiquitylating the REX1 transcription factor and is mutated in an X-linked intellectual disability disorder. However, the precise mechanisms by which ubiquitylation drives specific transcriptional responses are not known. Here, we show that RNF12 is recruited to specific genomic locations via a consensus sequence motif, which enables co-localisation with REX1 substrate at gene promoters. Surprisingly, RNF12 chromatin recruitment is achieved via a non-catalytic basic region and comprises a previously unappreciated N-terminal autoinhibitory mechanism. Furthermore, RNF12 chromatin targeting is critical for REX1 ubiquitylation and downstream RNF12-dependent gene regulation. Our results demonstrate a key role for chromatin in regulation of the RNF12-REX1 axis and provide insight into mechanisms by which protein ubiquitylation enables programming of gene expression.

摘要

蛋白质泛素化调节包括转录在内的关键生物过程。E3 泛素连接酶 RNF12/RLIM 就是一个很好的例子,它通过泛素化 REX1 转录因子来控制发育基因的表达,并且在 X 连锁智力障碍疾病中发生突变。然而,泛素化驱动特定转录反应的确切机制尚不清楚。在这里,我们表明 RNF12 通过一个共识序列基序被招募到特定的基因组位置,这使得它能够与 REX1 底物在基因启动子处共定位。令人惊讶的是,RNF12 的染色质募集是通过一个非催化的碱性区域实现的,并且包含了一个以前未被认识到的 N 端自动抑制机制。此外,RNF12 染色质靶向对于 REX1 的泛素化和下游 RNF12 依赖的基因调控至关重要。我们的研究结果表明染色质在 RNF12-REX1 轴的调控中起着关键作用,并为蛋白质泛素化如何实现基因表达编程的机制提供了深入的了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd1/10781586/d555d1ae8341/LSA-2023-02282_Fig1.jpg

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