Biochemical methods for analysis of kinetoplastid RNA editing.


Publication Type:

Journal Article

Source:

Methods, Volume 15, Issue 1, p.15-26 (1998)

Keywords:

Animals, Cell Fractionation, Dimerization, DNA, Kinetoplast, Endonucleases, Genetic Techniques, Ligases, Mitochondria, Ribonucleoproteins, RNA Editing, RNA Helicases, RNA Nucleotidyltransferases, RNA, Protozoan, Transcription, Genetic, Trypanosoma brucei brucei, Uridine Triphosphate

Abstract:

<p>RNA editing is a posttranscriptional process involving mRNAs [reviewed by K. Stuart et al. (1997) Microbiol. Mol. Biol. Rev. 61, 105-120; G. J. Arts and R. Benne (1996) Biochim. Biophys. Acta 1307, 39-54; and S. L. Hajduk and R. S. Sabatini (1996) in Molecular Biology of Parasitic Protozoa (Smith, D. S., and Parsons, M., Eds.), pp. 134-158, Oxford Univ. Press, Oxford] and tRNAs [K. M. Lonergan and M. Gray (1993) Science 259, 812-816] that has now been described in an increasing number of eukaryotic organisms. In this process sequences differ from their gene sequences by the addition, removal, or conversion of specific ribonucleotides. RNA editing was first described within the mitochondrion of kinetoplastid protozoa. Several of the mitochondrial mRNAs in these flagellates have uridine residues inserted and deleted at specific sites. In some cases, more than 50% of the mRNA is created by RNA editing. In this article, we describe some of the biochemical methods used in analyzing the process of RNA editing in kinetoplastid mitochondria.</p>