Key result
Polyadenylation of the PARP mRNA precursor in Trypanosoma brucei is coupled to downstream trans-splicing, with cryptic signals functioning only when dominant ones are deleted.
Polyadenylation in trypanosomes is coupled to downstream trans splicing, with a hierarchy of processing signals determining the site.
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No immediate implications for cardiovascular practice; leaves open whether similar mRNA processing hierarchies operate in human cells.
Nearly all trypanosome mRNAs are synthesized as polycistronic precursors, from which mature mRNAs are excised by trans splicing and polyadenylation. Polyadenylation of a procyclic acidic repetitive protein (PARP, or procyclin) transcript was studied by transient transfection of constructs bearing a chloramphenicol acetyltransferase gene linked to the PARP intergenic region. Polyadenylation usually occurred at A residues, about 100 bases upstream of a trans-splicing acceptor signal. The wild-type polyadenylation site has a cryptic trans-splicing signal about 100 bp downstream: deletion or inversion of this signal results in polyadenylation at multiple sites, upstream of other cryptic trans-splicing signals. The PARP mRNA precursor appears to contain a hierarchy of possible processing signals, the function of cryptic ones being revealed only when the dominant ones are deleted or moved. Correct polyadenylation can be restored by addition of trans-splicing signals from other loci. The results indicate that polyadenylation is coupled to downstream trans splicing but that the products of the trans-splicing reaction are not necessarily functional mRNAs.
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Hug et al. (1994) studied this question. Plasmid constructs with PARP intergenic region was evaluated on Polyadenylation site usage. Polyadenylation of the PARP mRNA precursor in Trypanosoma brucei is coupled to downstream trans-splicing, with cryptic signals functioning only when dominant ones are deleted.
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