| Literature DB >> 32191849 |
Inna Aphasizheva1, Juan Alfonzo2, Jason Carnes3, Igor Cestari4, Jorge Cruz-Reyes5, H Ulrich Göringer6, Stephen Hajduk7, Julius Lukeš8, Susan Madison-Antenucci9, Dmitri A Maslov10, Suzanne M McDermott3, Torsten Ochsenreiter11, Laurie K Read12, Reza Salavati4, Achim Schnaufer13, André Schneider14, Larry Simpson15, Kenneth Stuart3, Vyacheslav Yurchenko16, Z Hong Zhou15, Alena Zíková8, Liye Zhang17, Sara Zimmer18, Ruslan Aphasizhev19.
Abstract
Trypanosoma brucei spp. cause African human and animal trypanosomiasis, a burden on health and economy in Africa. These hemoflagellates are distinguished by a kinetoplast nucleoid containing mitochondrial DNAs of two kinds: maxicircles encoding ribosomal RNAs (rRNAs) and proteins and minicircles bearing guide RNAs (gRNAs) for mRNA editing. All RNAs are produced by a phage-type RNA polymerase as 3' extended precursors, which undergo exonucleolytic trimming. Most pre-mRNAs proceed through 3' adenylation, uridine insertion/deletion editing, and 3' A/U-tailing. The rRNAs and gRNAs are 3' uridylated. Historically, RNA editing has attracted major research effort, and recently essential pre- and postediting processing events have been discovered. Here, we classify the key players that transform primary transcripts into mature molecules and regulate their function and turnover.Entities:
Keywords: RNA decay; RNA editing; Trypanosoma; kinetoplast; mitochondria; polyadenylation
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Year: 2020 PMID: 32191849 PMCID: PMC7083771 DOI: 10.1016/j.pt.2020.01.006
Source DB: PubMed Journal: Trends Parasitol ISSN: 1471-4922