Cargando…

Novel organization of mitochondrial minicircles and guide RNAs in the zoonotic pathogen Trypanosoma lewisi

Kinetoplastid flagellates are known for several unusual features, one of which is their complex mitochondrial genome, known as kinetoplast (k) DNA, composed of mutually catenated maxi- and minicircles. Trypanosoma lewisi is a member of the Stercorarian group of trypanosomes which is, based on human...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Su-Jin, Zhang, Xuan, Lukeš, Julius, Li, Bi-Qi, Wang, Ju-Feng, Qu, Liang-Hu, Hide, Geoff, Lai, De-Hua, Lun, Zhao-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7515712/
https://www.ncbi.nlm.nih.gov/pubmed/32853372
http://dx.doi.org/10.1093/nar/gkaa700
_version_ 1783586858693820416
author Li, Su-Jin
Zhang, Xuan
Lukeš, Julius
Li, Bi-Qi
Wang, Ju-Feng
Qu, Liang-Hu
Hide, Geoff
Lai, De-Hua
Lun, Zhao-Rong
author_facet Li, Su-Jin
Zhang, Xuan
Lukeš, Julius
Li, Bi-Qi
Wang, Ju-Feng
Qu, Liang-Hu
Hide, Geoff
Lai, De-Hua
Lun, Zhao-Rong
author_sort Li, Su-Jin
collection PubMed
description Kinetoplastid flagellates are known for several unusual features, one of which is their complex mitochondrial genome, known as kinetoplast (k) DNA, composed of mutually catenated maxi- and minicircles. Trypanosoma lewisi is a member of the Stercorarian group of trypanosomes which is, based on human infections and experimental data, now considered a zoonotic pathogen. By assembling a total of 58 minicircle classes, which fall into two distinct categories, we describe a novel type of kDNA organization in T. lewisi. RNA-seq approaches allowed us to map the details of uridine insertion and deletion editing events upon the kDNA transcriptome. Moreover, sequencing of small RNA molecules enabled the identification of 169 unique guide (g) RNA genes, with two differently organized minicircle categories both encoding essential gRNAs. The unprecedented organization of minicircles and gRNAs in T. lewisi broadens our knowledge of the structure and expression of the mitochondrial genomes of these human and animal pathogens. Finally, a scenario describing the evolution of minicircles is presented.
format Online
Article
Text
id pubmed-7515712
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-75157122020-09-30 Novel organization of mitochondrial minicircles and guide RNAs in the zoonotic pathogen Trypanosoma lewisi Li, Su-Jin Zhang, Xuan Lukeš, Julius Li, Bi-Qi Wang, Ju-Feng Qu, Liang-Hu Hide, Geoff Lai, De-Hua Lun, Zhao-Rong Nucleic Acids Res Genomics Kinetoplastid flagellates are known for several unusual features, one of which is their complex mitochondrial genome, known as kinetoplast (k) DNA, composed of mutually catenated maxi- and minicircles. Trypanosoma lewisi is a member of the Stercorarian group of trypanosomes which is, based on human infections and experimental data, now considered a zoonotic pathogen. By assembling a total of 58 minicircle classes, which fall into two distinct categories, we describe a novel type of kDNA organization in T. lewisi. RNA-seq approaches allowed us to map the details of uridine insertion and deletion editing events upon the kDNA transcriptome. Moreover, sequencing of small RNA molecules enabled the identification of 169 unique guide (g) RNA genes, with two differently organized minicircle categories both encoding essential gRNAs. The unprecedented organization of minicircles and gRNAs in T. lewisi broadens our knowledge of the structure and expression of the mitochondrial genomes of these human and animal pathogens. Finally, a scenario describing the evolution of minicircles is presented. Oxford University Press 2020-08-27 /pmc/articles/PMC7515712/ /pubmed/32853372 http://dx.doi.org/10.1093/nar/gkaa700 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Genomics
Li, Su-Jin
Zhang, Xuan
Lukeš, Julius
Li, Bi-Qi
Wang, Ju-Feng
Qu, Liang-Hu
Hide, Geoff
Lai, De-Hua
Lun, Zhao-Rong
Novel organization of mitochondrial minicircles and guide RNAs in the zoonotic pathogen Trypanosoma lewisi
title Novel organization of mitochondrial minicircles and guide RNAs in the zoonotic pathogen Trypanosoma lewisi
title_full Novel organization of mitochondrial minicircles and guide RNAs in the zoonotic pathogen Trypanosoma lewisi
title_fullStr Novel organization of mitochondrial minicircles and guide RNAs in the zoonotic pathogen Trypanosoma lewisi
title_full_unstemmed Novel organization of mitochondrial minicircles and guide RNAs in the zoonotic pathogen Trypanosoma lewisi
title_short Novel organization of mitochondrial minicircles and guide RNAs in the zoonotic pathogen Trypanosoma lewisi
title_sort novel organization of mitochondrial minicircles and guide rnas in the zoonotic pathogen trypanosoma lewisi
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7515712/
https://www.ncbi.nlm.nih.gov/pubmed/32853372
http://dx.doi.org/10.1093/nar/gkaa700
work_keys_str_mv AT lisujin novelorganizationofmitochondrialminicirclesandguidernasinthezoonoticpathogentrypanosomalewisi
AT zhangxuan novelorganizationofmitochondrialminicirclesandguidernasinthezoonoticpathogentrypanosomalewisi
AT lukesjulius novelorganizationofmitochondrialminicirclesandguidernasinthezoonoticpathogentrypanosomalewisi
AT libiqi novelorganizationofmitochondrialminicirclesandguidernasinthezoonoticpathogentrypanosomalewisi
AT wangjufeng novelorganizationofmitochondrialminicirclesandguidernasinthezoonoticpathogentrypanosomalewisi
AT qulianghu novelorganizationofmitochondrialminicirclesandguidernasinthezoonoticpathogentrypanosomalewisi
AT hidegeoff novelorganizationofmitochondrialminicirclesandguidernasinthezoonoticpathogentrypanosomalewisi
AT laidehua novelorganizationofmitochondrialminicirclesandguidernasinthezoonoticpathogentrypanosomalewisi
AT lunzhaorong novelorganizationofmitochondrialminicirclesandguidernasinthezoonoticpathogentrypanosomalewisi