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J. Biol. Chem., Vol. 262, Issue 33, 16192-16199, Nov, 1987
A Gabriel, SS Sisodia and DW Cleveland
In an effort to exploit the advantages of Crithidia fasciculata for
detailed analysis of the mechanisms of discontinuous transcription in the
trypanosomatid family, we have cloned, sequenced, and characterized the
mini-exon gene repeat in Crithidia and mapped the termini of its primary
transcript. We find that Crithidia contains approximately 500 mini-exon
genes, present almost exclusively as tandemly repeated arrays on a single
chromosome. Transcripts derived from these genes are approximately 90 bases
in length with heterogeneity at both the 5' and 3' ends. Primer extension
experiments reveal a putative splicing intermediate. Specific inhibition of
in vitro translation of Crithidia mRNAs by an oligonucleotide complementary
to the mini-exon suggests that all Crithidia mRNAs contain the mini-exon at
their 5' termini. Comparison of mini-exon gene sequences from various
trypanosomatids reveals several regions of conservation that imply
functional constraints on the transcription of mini-exon genes and the
processing of their transcripts.
Evidence of discontinuous transcription in the trypanosomatid Crithidia fasciculata
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
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