Mitochondrial RNA editing in Trypanoplasma borreli: New tools, new revelations
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17310%2F22%3AA2402NBT" target="_blank" >RIV/61988987:17310/22:A2402NBT - isvavai.cz</a>
Alternative codes found
RIV/60077344:_____/22:00567811 RIV/60076658:12310/22:43906095
Result on the web
<a href="https://www.sciencedirect.com/science/article/pii/S2001037022005177" target="_blank" >https://www.sciencedirect.com/science/article/pii/S2001037022005177</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.csbj.2022.11.023" target="_blank" >10.1016/j.csbj.2022.11.023</a>
Alternative languages
Result language
angličtina
Original language name
Mitochondrial RNA editing in Trypanoplasma borreli: New tools, new revelations
Original language description
The kinetoplastids are unicellular flagellates that derive their name from the 'kinetoplast', a region within their single mitochondrion harboring its organellar genome of high DNA content, called kinetoplast (k) DNA. Some protein products of this mitochondrial genome are encoded as cryptogenes; their transcripts require editing to generate an open reading frame. This happens through RNA editing, whereby small regulatory guide (g)RNAs direct the proper insertion and deletion of one or more uridines at each editing site within specific transcript regions. An accurate perspective of the kDNA expansion and evolution of their unique uridine insertion/deletion editing across kinetoplastids has been difficult to achieve. Here, we resolved the kDNA structure and editing patterns in the early-branching kinetoplastid Trypanoplasma borreli and compare them with those of the well-studied trypanosomatids. We find that its kDNA consists of circular molecules of about 42 kb that harbor the rRNA and protein-coding genes, and 17 different contigs of approximately 70 kb carrying an average of 23 putative gRNA loci per contig. These contigs may be linear molecules, as they contain repetitive termini. Our analysis uncovered a putative gRNA population with unique length and sequence parameters that is massive relative to the editing needs of this parasite. We validated or determined the sequence identity of four edited mRNAs, including one coding for ATP synthase 6 that was previously thought to be missing. We utilized computational methods to show that the T. borreli transcriptome includes a substantial number of transcripts with inconsistent editing patterns, apparently products of non-canonical editing. This species utilizes the most extensive uridine deletion compared to other studied kinetoplastids to enforce amino acid conservation of cryptogene products, although insertions still remain more frequent.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10608 - Biochemistry and molecular biology
Result continuities
Project
<a href="/en/project/GA22-01026S" target="_blank" >GA22-01026S: RNA editing in non-model flagellates</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL
ISSN
2001-0370
e-ISSN
—
Volume of the periodical
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Issue of the periodical within the volume
2022
Country of publishing house
SE - SWEDEN
Number of pages
14
Pages from-to
6388-6402
UT code for WoS article
001043880900008
EID of the result in the Scopus database
2-s2.0-85142138566