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Lexis and Grammar of Mitochondrial RNA Processing in Trypanosomes. | LitMetric

AI Article Synopsis

  • Trypanosoma brucei species cause African sleeping sickness and other diseases, impacting health and economies in Africa.
  • These parasites possess a unique kinetoplast with two types of mitochondrial DNA that encode crucial components for cellular processes, including ribosomal RNAs and guide RNAs for mRNA editing.
  • Recent research highlights the complex RNA editing mechanisms in these parasites, focusing on the processing of primary transcripts into mature forms and how these processes are regulated.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083771PMC
http://dx.doi.org/10.1016/j.pt.2020.01.006DOI Listing

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