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(Received for publication, April 14, 1995; and in revised form, June 28,
1995) 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.
Volume 270,
Number 37,
Issue of September 15, pp. 21813-21819, 1995
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
ANALYSIS OF TRANS-SPLICED mRNAs AND GENES IN THE HUMAN PARASITE, SCHISTOSOMA MANSONI
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