Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Trypanosoma cruzi strain and starvation-driven mitochondrial RNA editing and transcriptome variability

ES. Gerasimov, R. Ramirez-Barrios, V. Yurchenko, SL. Zimmer

. 2022 ; 28 (7) : 993-1012. [pub] 20220425

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc22017927
E-zdroje Online Plný text

NLK Free Medical Journals od 1995 do Před 6 měsíci
PubMed Central od 1995 do Před 1 rokem
Europe PubMed Central od 1995 do Před 1 rokem
Open Access Digital Library od 1995-03-01

Trypanosoma cruzi is a unicellular protistan parasitic species that is comprised of strains and isolates exhibiting high levels of genetic and metabolic variability. In the insect vector, it is known to be highly responsive to starvation, a signal for progression to a life stage in which it can infect mammalian cells. Most mRNAs encoded in its mitochondrion require the targeted insertion and deletion of uridines to become translatable transcripts. This study defined differences in uridine-insertion/deletion RNA editing among three strains and established the mechanism whereby abundances of edited (and, thus, translatable) mitochondrial gene products increase during starvation. Our approach utilized our custom T-Aligner toolkit to describe transcriptome-wide editing events and reconstruct editing products from high-throughput sequencing data. We found that the relative abundance of mitochondrial transcripts and the proportion of mRNAs that are edited varies greatly between analyzed strains, a characteristic that could potentially impact metabolic capacity. Starvation typically led to an increase in overall editing activity rather than affecting a specific step in the process. We also determined that transcripts CR3, CR4, and ND3 produce multiple open reading frames that, if translated, would generate different proteins. Finally, we quantitated the inherent flexibility of editing in T. cruzi and found it to be higher relative to that in a related trypanosomatid lineage. Over time, new editing domains or patterns could prove advantageous to the organism and become more widespread within individual transcriptomes or among strains.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc22017927
003      
CZ-PrNML
005      
20220804134451.0
007      
ta
008      
220720s2022 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1261/rna.079088.121 $2 doi
035    __
$a (PubMed)35470233
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Gerasimov, Evgeny S $u Faculty of Biology, M.V. Lomonosov Moscow State University, Moscow 119991, Russia $u Institute for Information Transmission Problems, Russian Academy of Sciences, Moscow 127051, Russia $1 https://orcid.org/0000000204971221
245    10
$a Trypanosoma cruzi strain and starvation-driven mitochondrial RNA editing and transcriptome variability / $c ES. Gerasimov, R. Ramirez-Barrios, V. Yurchenko, SL. Zimmer
520    9_
$a Trypanosoma cruzi is a unicellular protistan parasitic species that is comprised of strains and isolates exhibiting high levels of genetic and metabolic variability. In the insect vector, it is known to be highly responsive to starvation, a signal for progression to a life stage in which it can infect mammalian cells. Most mRNAs encoded in its mitochondrion require the targeted insertion and deletion of uridines to become translatable transcripts. This study defined differences in uridine-insertion/deletion RNA editing among three strains and established the mechanism whereby abundances of edited (and, thus, translatable) mitochondrial gene products increase during starvation. Our approach utilized our custom T-Aligner toolkit to describe transcriptome-wide editing events and reconstruct editing products from high-throughput sequencing data. We found that the relative abundance of mitochondrial transcripts and the proportion of mRNAs that are edited varies greatly between analyzed strains, a characteristic that could potentially impact metabolic capacity. Starvation typically led to an increase in overall editing activity rather than affecting a specific step in the process. We also determined that transcripts CR3, CR4, and ND3 produce multiple open reading frames that, if translated, would generate different proteins. Finally, we quantitated the inherent flexibility of editing in T. cruzi and found it to be higher relative to that in a related trypanosomatid lineage. Over time, new editing domains or patterns could prove advantageous to the organism and become more widespread within individual transcriptomes or among strains.
650    _2
$a zvířata $7 D000818
650    _2
$a savci $x genetika $7 D008322
650    _2
$a protozoální proteiny $x genetika $x metabolismus $7 D015800
650    _2
$a RNA $x metabolismus $7 D012313
650    _2
$a editace RNA $7 D017393
650    _2
$a messenger RNA $x genetika $x metabolismus $7 D012333
650    _2
$a RNA mitochondriální $x genetika $x metabolismus $7 D000077278
650    _2
$a RNA protozoální $x genetika $x metabolismus $7 D016053
650    _2
$a transkriptom $7 D059467
650    12
$a Trypanosoma brucei brucei $x genetika $7 D014346
650    12
$a Trypanosoma cruzi $x genetika $x metabolismus $7 D014349
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Ramirez-Barrios, Roger $u Department of Biomedical Sciences, University of Minnesota Medical School, Duluth Campus, Duluth, Minnesota 55812, USA $1 https://orcid.org/0000000247246724
700    1_
$a Yurchenko, Vyacheslav $u Life Science Research Centre, Faculty of Science, University of Ostrava, 710 00 Ostrava, Czech Republic $u Martsinovsky Institute of Medical Parasitology, Tropical and Vector Borne Diseases, Sechenov University, Moscow 119435, Russia $1 https://orcid.org/0000000347653263 $7 xx0234303
700    1_
$a Zimmer, Sara L $u Department of Biomedical Sciences, University of Minnesota Medical School, Duluth Campus, Duluth, Minnesota 55812, USA $1 https://orcid.org/0000000217071839
773    0_
$w MED00006007 $t RNA (New York, N.Y.) $x 1469-9001 $g Roč. 28, č. 7 (2022), s. 993-1012
856    41
$u https://pubmed.ncbi.nlm.nih.gov/35470233 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y p $z 0
990    __
$a 20220720 $b ABA008
991    __
$a 20220804134445 $b ABA008
999    __
$a ok $b bmc $g 1821834 $s 1169170
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2022 $b 28 $c 7 $d 993-1012 $e 20220425 $i 1469-9001 $m RNA $n RNA $x MED00006007
LZP    __
$a Pubmed-20220720

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...