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

被引:1
|
作者
Espejo-Serrano, Carmen [1 ]
Aitken, Catriona [1 ]
Tan, Beatrice F. [2 ]
May, Danielle G. [3 ]
Chrisopulos, Rachel J. [3 ]
Roux, Kyle J. [3 ,4 ]
Demmers, Jeroen A. A. [5 ,6 ]
Mackintosh, Samuel G. [7 ]
Gribnau, Joost [2 ]
Bustos, Francisco [4 ,8 ]
Gontan, Cristina [2 ]
Findlay, Greg M. [3 ]
机构
[1] Univ Dundee, Sch Life Sci, MRC Prot Phosphorylat & Ubiquitylat Unit, Dundee, Scotland
[2] Erasmus MC, Dept Dev Biol, Rotterdam, Netherlands
[3] Sanford Res, Enabling Technol Grp, Sioux Falls, SD 57104 USA
[4] Univ South Dakota, Sanford Sch Med, Dept Pediat, Sioux Falls, SD USA
[5] Erasmus MC, Prote Ctr, Rotterdam, Netherlands
[6] Erasmus MC, Dept Biochem, Rotterdam, Netherlands
[7] Univ Arkansas Med Sci, Dept Biochem & Mol Biol, Little Rock, AR USA
[8] Sanford Res, Pediat & Rare Dis Grp, Sioux Falls, SD USA
基金
英国惠康基金; 荷兰研究理事会; 美国国家卫生研究院;
关键词
X-CHROMOSOME INACTIVATION; UBIQUITYLATION; RLIM/RNF12;
D O I
10.26508/lsa.202302282
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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收藏
页数:19
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