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Volume 270, Number 37, Issue of September 15, pp. 21813-21819, 1995
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
RNA Trans-splicing in Flatworms
ANALYSIS OF TRANS-SPLICED mRNAs AND GENES IN THE HUMAN PARASITE, SCHISTOSOMA MANSONI

(Received for publication, April 14, 1995; and in revised form, June 28, 1995)

Richard E. Davis Cara Hardwick Paul Tavernier ,&nbsp;<WBR> Scott Hodgson Hardeep Singh

Characteristics of trans-splicing in Schistosoma mansoni were examined to explore the significance and determinants of spliced leader (SL) addition in flatworms. Only a small subset of mRNAs acquire the SL. Analysis of 30 trans-spliced mRNAs and four genes revealed no discernable patterns or common characteristics in the genes, mRNAs, or their encoded proteins that might explain the functional significance of SL addition. While the mRNA encoding the glycolytic enzyme enolase is trans-spliced, mRNAs encoding four other glycolytic enzymes are not, indicating trans-splicing is not prevalent throughout this metabolic pathway. Although the 3` end of flatworm SLs contribute an AUG to mRNAs, the SL AUG does not typically serve to provide a methionine for translation initiation of reading frames in recipient mRNAs. SL RNA expression exhibits no apparent sex, tissue, or cell specificity. Trans-spliced genes undergo both cis- and trans-splicing, and the sequence contexts for these respective acceptor sites are very similar. These results suggest trans-splicing in flatworms is most likely associated either with some property conferred on recipient mRNAs by SL addition or related to some characteristic of the primary transcripts or transcription of trans-spliced genes.




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