TY - JOUR
T1 - Blastocrithidia nonstop mitochondrial genome and its expression are remarkably insulated from nuclear codon reassignment
AU - Afonin, Dmitry A.
AU - Gerasimov, Evgeny S.
AU - Škodová-Sveráková, Ingrid
AU - Záhonová, Kristína
AU - Gahura, Ondřej
AU - Albanaz, Amanda T.S.
AU - Myšková, Eva
AU - Bykova, Anastassia
AU - Paris, Zdeněk
AU - Lukeš, Julius
AU - Opperdoes, Fred R.
AU - Horváth, Anton
AU - Zimmer, Sara L.
AU - Yurchenko, Vyacheslav
N1 - Publisher Copyright:
© The Author(s) 2024. Published by Oxford University Press on behalf of Nucleic Acids Research.
PY - 2024/4/24
Y1 - 2024/4/24
N2 - The canonical stop codons of the nuclear genome of the trypanosomatid Blastocrithidia nonstop are recoded. Here, we investigated the effect of this recoding on the mitochondrial genome and gene expression. Trypanosomatids possess a single mitochondrion and protein-coding transcripts of this genome require RNA editing in order to generate open reading frames of many transcripts encoded as 'cryptogenes'. Small RNAs that can number in the hundreds direct editing and produce a mitochondrial transcriptome of unusual complexity. We find B. nonstop to have a typical trypanosomatid mitochondrial genetic code, which presumably requires the mitochondrion to disable utilization of the two nucleus-encoded suppressor tRNAs, which appear to be imported into the organelle. Alterations of the protein factors responsible for mRNA editing were also documented, but they have likely originated from sources other than B. nonstop nuclear genome recoding. The population of guide RNAs directing editing is minimal, yet virtually all genes for the plethora of known editing factors are still present. Most intriguingly, despite lacking complex I cryptogene guide RNAs, these cryptogene transcripts are stochastically edited to high levels.
AB - The canonical stop codons of the nuclear genome of the trypanosomatid Blastocrithidia nonstop are recoded. Here, we investigated the effect of this recoding on the mitochondrial genome and gene expression. Trypanosomatids possess a single mitochondrion and protein-coding transcripts of this genome require RNA editing in order to generate open reading frames of many transcripts encoded as 'cryptogenes'. Small RNAs that can number in the hundreds direct editing and produce a mitochondrial transcriptome of unusual complexity. We find B. nonstop to have a typical trypanosomatid mitochondrial genetic code, which presumably requires the mitochondrion to disable utilization of the two nucleus-encoded suppressor tRNAs, which appear to be imported into the organelle. Alterations of the protein factors responsible for mRNA editing were also documented, but they have likely originated from sources other than B. nonstop nuclear genome recoding. The population of guide RNAs directing editing is minimal, yet virtually all genes for the plethora of known editing factors are still present. Most intriguingly, despite lacking complex I cryptogene guide RNAs, these cryptogene transcripts are stochastically edited to high levels.
UR - https://www.scopus.com/pages/publications/85191398222
UR - https://www.scopus.com/pages/publications/85191398222#tab=citedBy
U2 - 10.1093/nar/gkae168
DO - 10.1093/nar/gkae168
M3 - Article
C2 - 38452217
AN - SCOPUS:85191398222
SN - 0305-1048
VL - 52
SP - 3870
EP - 3885
JO - Nucleic acids research
JF - Nucleic acids research
IS - 7
ER -