GERASIMOV, E.S., A.A. GASPARYAN, I. KAUROV, Boris TICHÝ, M.D. LOGACHEVA, A.A. KOLESNIKOV, J. LUKES, V. YURCHENKO, S.L. ZIMMER and P. FLEGONTOV. Trypanosomatid mitochondrial RNA editing: dramatically complex transcript repertoires revealed with a dedicated mapping tool. Nucleic Acids Research. Oxford: Oxford University Press, 2018, vol. 46, No 2, p. 765-781. ISSN 0305-1048. Available from: https://dx.doi.org/10.1093/nar/gkx1202.
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Basic information
Original name Trypanosomatid mitochondrial RNA editing: dramatically complex transcript repertoires revealed with a dedicated mapping tool
Authors GERASIMOV, E.S. (643 Russian Federation), A.A. GASPARYAN (643 Russian Federation), I. KAUROV (643 Russian Federation), Boris TICHÝ (203 Czech Republic, guarantor, belonging to the institution), M.D. LOGACHEVA (643 Russian Federation), A.A. KOLESNIKOV (643 Russian Federation), J. LUKES (203 Czech Republic), V. YURCHENKO (203 Czech Republic), S.L. ZIMMER (840 United States of America) and P. FLEGONTOV (643 Russian Federation).
Edition Nucleic Acids Research, Oxford, Oxford University Press, 2018, 0305-1048.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10608 Biochemistry and molecular biology
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 11.147
RIV identification code RIV/00216224:14740/18:00102931
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1093/nar/gkx1202
UT WoS 000423812300027
Keywords in English AUG INITIATION CODONS; MESSENGER-RNA; INSECT TRYPANOSOMATIDS; LEISHMANIA-TARENTOLAE; LEPTOMONAS-PYRRHOCORIS; CRITHIDIA-FASCICULATA; GENE-EXPRESSION; BRUCEI; EVOLUTION; CRYPTOGENE
Tags rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Pavla Foltynová, Ph.D., učo 106624. Changed: 13/3/2019 11:36.
Abstract
RNA editing by targeted insertion and deletion of uridine is crucial to generate translatable mRNAs from the cryptogenes of the mitochondrial genome of kinetoplastids. This type of editing consists of a stepwise cascade of reactions generally proceeding from 3' to 5' on a transcript, resulting in a population of partially edited as well as pre-edited and completely edited molecules for each mitochondrial cryptogene of these protozoans. Often, the number of uridines inserted and deleted exceed the number of nucleotides that are genome-encoded. Thus, analysis of kinetoplastid mitochondrial transcriptomes has proven frustratingly complex. Here we present our analysis of Leptomonas pyrrhocoris mitochondrial cDNA deep sequencing reads using T-Aligner, our new tool which allows comprehensive characterization of RNA editing, not relying on targeted transcript amplification and on prior knowledge of final edited products. T-Aligner implements a pipeline of read mapping, visualization of all editing states and their coverage, and assembly of canonical and alternative translatable mRNAs. We also assess T-Aligner functionality on a more challenging deep sequencing read input from Trypanosoma cruzi. The analysis reveals that transcripts of cryptogenes of both species undergo very complex editing that includes the formation of alternative open reading frames and whole categories of truncated editing products.
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