A novel interaction between RNA m6A methyltransferase METTL3 and RREB1

被引:0
|
作者
Xu, Jing [1 ]
Sivakumar, Charukesi [1 ,2 ]
Ryan, Charles W. [3 ]
Rao, Rajesh C. [1 ,2 ,4 ,5 ,6 ,7 ,8 ,9 ]
机构
[1] Univ Michigan, WK Kellogg Eye Ctr, Dept Ophthalmol & Visual Sci, Ann Arbor, MI 48105 USA
[2] Univ Michigan, Dept Pathol, Ann Arbor, MI 48105 USA
[3] Univ Michigan, Med Sch, Med Scientist Training Program, Ann Arbor, MI 48105 USA
[4] Univ Michigan, Dept Human Genet, Ann Arbor, MI 48105 USA
[5] Univ Michigan, Rogel Canc Ctr, Ann Arbor, MI 48105 USA
[6] Univ Michigan, Ctr Computat Med & Bioinformat, Ann Arbor, MI 48105 USA
[7] Univ Michigan, Ctr RNA Biomed, Ann Arbor, MI 48105 USA
[8] Univ Michigan, A Alfred Taubman Med Res Inst, Ann Arbor, MI 48105 USA
[9] Vet Adm Ann Arbor Healthcare Syst, Surg Serv, Sect Ophthalmol, Ann Arbor, MI 48105 USA
关键词
TRANSCRIPTION FACTOR RREB1; ZINC-FINGER PROTEIN; RAS; TRANSLATION; GENE;
D O I
10.1016/j.bbrc.2024.150668
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Regulation of gene expression is achieved through the modulation of regulatory inputs both pre- and post-transcriptionally. Methyltransferase-like 3 (METTL3) is a key player in pre-mRNA processing, actively catalyzing N6-methyladenosine (m6A). Among the most enriched mRNA targets of METTL3 is the Ras Responsive Element Binding Protein 1 (RREB1), a transcription factor which functions to govern cell fate, proliferation and DNA repair. Here, we show a novel interaction between METTL3 and RREB1. Further examination of this interaction indicates that METTL3's N-terminus is the primary interacting domain. Our findings uncover a novel interacting partner of METTL3, providing further insights into METTL3's regulatory network.
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页数:5
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