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Molecular and Cellular Biology, August 2002, p. 5337-5346, Vol. 22, No. 15
0270-7306/02/$04.00+0 DOI: 10.1128/MCB.22.15.5337-5346.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Center for RNA Molecular Biology, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106
Received 4 March 2002/ Returned for modification 17 April 2002/ Accepted 24 April 2002
The trans-splicing reaction involves the association of 5'; and 3'; splice sites contained on separate transcripts. The mechanism by which these splice sites are juxtaposed during trans-spliceosome assembly and the role of SR proteins at each stage in this process have not been determined. Utilizing a system that allows for the separation of the RNA binding and RS domains of SR proteins, we have found that SR proteins are required for at least two stages of the trans-splicing reaction. They are important both prior to and subsequent to the addition of U2 snRNP to the 3'; acceptor. In addition, we have demonstrated a role for RS domain phosphorylation in both of these activities. Dephosphorylation of the RS domain led to a block in U2 snRNP binding to the substrate. In a separate experiment, RS domain phosphorylation was also determined to be necessary for trans splicing to proceed on a substrate that had U2 snRNP already bound. This newly identified role for phosphorylated SR proteins post-U2-snRNP addition coincides with the recruitment of the 5'; splice site contained on the SL RNP, suggesting a role for SR proteins in splice site communication in trans splicing.
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