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Many trypanosome messenger RNAs share a common 5′ terminal sequence
Author(s) -
Titia de Lange,
Paul A.M. Michels,
Hary J.G. Veerman,
Albert W.C.A. Cornelissen,
Piet Borst
Publication year - 1984
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/12.9.3777
Subject(s) - biology , exon , exon trapping , genetics , polyadenylation , gene , nucleic acid sequence , microbiology and biotechnology , repeated sequence , alu element , exon shuffling , tandem exon duplication , rna , alternative splicing , human genome , genome
The mRNAs for different variant surface antigens of Trypanosoma brucei start with the same 35 nucleotides. This sequence is encoded by a separate mini-exon, located in a 1.35-kb repetitive element. We have reported that trypanosomes contain many transcripts that hybridize to mini-exon probes, even if they do not make the surface antigens. We show here that these transcripts have the mini-exon sequence at their 5' end; they do not contain other sequences from the mini-exon repeat element and are polyadenylated. We have cloned DNA complementary to trypanosome mRNAs and randomly selected 17 clones containing mini-exon sequences. Thirteen of these are derived from different genes that do not code for surface antigens. We conclude that the mini-exon sequence is a common element at the 5' end of many trypanosome mRNAs. As the 200 genes for mini-exons are highly clustered, linkage of the mini-exon sequence to the remainder of most mRNAs may require discontinuous transcription.

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