Splicing factor U2AF2 promotes inclusion of exons with poor nucleosome phasing
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA1126206 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR33155610_1.fastq.gz | Fastqsanger.gz | |||
| SRR33155610_2.fastq.gz | Fastqsanger.gz | |||
| SRR33155611_1.fastq.gz | Fastqsanger.gz | |||
| SRR33155611_2.fastq.gz | Fastqsanger.gz | |||
| SRR33155612_1.fastq.gz | Fastqsanger.gz |
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Project description:Alternative splicing drives transcriptome and proteome diversification. While splicing regulatory proteins govern this process, their global mechanisms remain enigmatic. We generated high resolution transcriptome-wide protein-RNA interaction maps to determine how the splicing repressor hnRNPA1 influences the global association of spliceosome assembly factor U2AF2 and SRSF1 with pre-mRNA. We observed changes in the distribution of U2AF2 crosslinking sites relative to the 3’ splice sites of cassette exons but not constitutive exons upon hnRNPA1 overexpression. By contrast, SRSF1 crosslinking patterns relative to splice sites are independent of hnRNPA1 expression levels. We also observed an hnRNPA1-dependent increase in U2AF2 but not SRSF1 crosslinking to exon proximal antisense Alu elements. Thus Alu elements can serve as splicing factor-responsive sinks for U2AF2. These results not only demonstrate a novel mechanism for alternative splicing regulation but also implicate retrotransposon-derived sequences in the evolution of species-specific alternative splicing.
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