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The splicing factor SRp20 modifies splicing of its own mRNA and ASF/SF2 antagonizes this regulation.
Jumaa, H; Nielsen, P J.
Affiliation
  • Jumaa H; Max Planck Institute for Immunobiology, Freiburg, Germany.
EMBO J ; 16(16): 5077-85, 1997 Aug 15.
Article in En | MEDLINE | ID: mdl-9305649
ABSTRACT
SRp20 is a member of the highly conserved SR family of splicing regulators. Using a variety of reporter gene constructs, we show that SRp20 regulates alternative splicing of its own mRNA. Overexpression of SRp20 results in a reduction in the level of exon 4-skipped SRp20 transcripts and activates the production of transcripts containing exon 4. These exon 4-included transcripts encode a truncated protein lacking the C-terminal RS domain. We provide evidence that SRp20 probably enhances the recognition of the otherwise unused, weak splice acceptor of exon 4. The recognition of exons with weak splice acceptor sites may be a general activity of SRp20. Unexpectedly, ASF/SF2, another member of the SR family, antagonizes the effect of SRp20 on SRp20 pre-mRNA splicing and suppresses the production of the exon 4-included form. Our results indicate that ASF/SF2 suppresses the use of the alternative exon 4, most likely by inhibiting the recognition of the splice donor of exon 4. These results demonstrate, for the first time, an auto-regulatory activity of an SR protein which is antagonized by a second SR protein.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: RNA, Messenger / Nuclear Proteins / RNA-Binding Proteins / Alternative Splicing Limits: Animals Language: En Year: 1997 Type: Article

Full text: 1 Database: MEDLINE Main subject: RNA, Messenger / Nuclear Proteins / RNA-Binding Proteins / Alternative Splicing Limits: Animals Language: En Year: 1997 Type: Article