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Identification of SRSF3 target mRNAs using inducible TRIBE.

Authors :
Jin, Siqian
Xue, Ziwei
Zhang, Jinchun
Wang, Ziqi
Zhang, Jin
Chen, Di
Liu, Wanlu
Lin, Junxin
Source :
Biochemical & Biophysical Research Communications. Nov2021, Vol. 578, p21-27. 7p.
Publication Year :
2021

Abstract

Serine and arginine-rich splicing factor 3 (SRSF3), the smallest member of the Ser/Arg-rich (SR) RNA-binding protein family, regulates multiple aspects of post-transcriptional gene expression program. Although SRSF3 is essential for early embryo development, reprogramming, and pluripotency maintenance, the RNA targets and specificity of RNA recognition of SRSF3 are not well understood in human pluripotent stem cells. In this study, we used inducible TRIBE (targets of RNA binding sites by editing) to identify RNA targets and binding motifs of SRSF3 in human embryonic stem cells (hESCs). We identified 3888 confident binding sites of SRSF3, corresponding to 1222 gene targets. Our results showed that nearly half of the binding sites were distributed in exons, reflecting the alternative splicing function of SRSF3. Motif analysis demonstrated that two of the SRSF3 recognition sequences were the same as the motifs identified in mouse embryonic stem cells, suggesting the recognition sequences of SRSF3 may be conserved in mammals. Overall, our analyses revealed the RNA targets of SRSF3 and uncovered its RNA recognition specificity, providing a valuable resource for understanding the function of SRSF3 in human embryonic stem cells. SRSF3 shows the characteristics of exon-specific binding preference. SRSF3 binds to pluripotency-related genes, indicating it important for hESC pluripotency maintenance. The motif of SRSF3 shows conservation between human and mouse. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0006291X
Volume :
578
Database :
Academic Search Index
Journal :
Biochemical & Biophysical Research Communications
Publication Type :
Academic Journal
Accession number :
152814722
Full Text :
https://doi.org/10.1016/j.bbrc.2021.09.019