| Literature DB >> 26727667 |
Henrik Koch1, Monika Raabe2, Henning Urlaub2,3, Albrecht Bindereif1, Christian Preußer1.
Abstract
The generation of mature mRNA in the protozoan parasite Trypanosoma brucei requires coupled polyadenylation and trans splicing. In contrast to other eukaryotes, we still know very little on components, mechanisms, and dynamics of the 3' end-processing machinery in trypanosomes. To characterize the catalytic core of the polyadenylation complex in T. brucei, we first identified the poly(A) polymerase [Tb927.7.3780] as the major functional, nuclear-localized enzyme in trypanosomes. In contrast, another poly(A) polymerase, encoded by an intron-containing gene [Tb927.3.3160], localizes mainly in the cytoplasm and appears not to be functional in general 3' end processing of mRNAs. Based on tandem-affinity purification with tagged CPSF160 and mass spectrometry, we identified ten associated components of the trypanosome polyadenylation complex, including homologues to all four CPSF subunits, Fip1, CstF50/64, and Symplekin, as well as two hypothetical proteins. RNAi-mediated knockdown revealed that most of these factors are essential for growth and required for both in vivo polyadenylation and trans splicing, arguing for a general coupling of these two mRNA-processing reactions.Entities:
Keywords: CPSF; Trypanosoma brucei; mRNA processing; poly(A) polymerase; polyadenylation; trans splicing
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Year: 2016 PMID: 26727667 PMCID: PMC4829303 DOI: 10.1080/15476286.2015.1130208
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.652