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Systematically fragmented genes in a multipartite mitochondrial genome

Arguably, the most bizarre mitochondrial DNA (mtDNA) is that of the euglenozoan eukaryote Diplonema papillatum. The genome consists of numerous small circular chromosomes none of which appears to encode a complete gene. For instance, the cox1 coding sequence is spread out over nine different chromos...

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Detalles Bibliográficos
Autores principales: Vlcek, Cestmir, Marande, William, Teijeiro, Shona, Lukeš, Julius, Burger, Gertraud
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3035467/
https://www.ncbi.nlm.nih.gov/pubmed/20935050
http://dx.doi.org/10.1093/nar/gkq883
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author Vlcek, Cestmir
Marande, William
Teijeiro, Shona
Lukeš, Julius
Burger, Gertraud
author_facet Vlcek, Cestmir
Marande, William
Teijeiro, Shona
Lukeš, Julius
Burger, Gertraud
author_sort Vlcek, Cestmir
collection PubMed
description Arguably, the most bizarre mitochondrial DNA (mtDNA) is that of the euglenozoan eukaryote Diplonema papillatum. The genome consists of numerous small circular chromosomes none of which appears to encode a complete gene. For instance, the cox1 coding sequence is spread out over nine different chromosomes in non-overlapping pieces (modules), which are transcribed separately and joined to a contiguous mRNA by trans-splicing. Here, we examine how many genes are encoded by Diplonema mtDNA and whether all are fragmented and their transcripts trans-spliced. Module identification is challenging due to the sequence divergence of Diplonema mitochondrial genes. By employing most sensitive protein profile search algorithms and comparing genomic with cDNA sequence, we recognize a total of 11 typical mitochondrial genes. The 10 protein-coding genes are systematically chopped up into three to 12 modules of 60–350 bp length. The corresponding mRNAs are all trans-spliced. Identification of ribosomal RNAs is most difficult. So far, we only detect the 3′-module of the large subunit ribosomal RNA (rRNA); it does not trans-splice with other pieces. The small subunit rRNA gene remains elusive. Our results open new intriguing questions about the biochemistry and evolution of mitochondrial trans-splicing in Diplonema.
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spelling pubmed-30354672011-02-08 Systematically fragmented genes in a multipartite mitochondrial genome Vlcek, Cestmir Marande, William Teijeiro, Shona Lukeš, Julius Burger, Gertraud Nucleic Acids Res Genomics Arguably, the most bizarre mitochondrial DNA (mtDNA) is that of the euglenozoan eukaryote Diplonema papillatum. The genome consists of numerous small circular chromosomes none of which appears to encode a complete gene. For instance, the cox1 coding sequence is spread out over nine different chromosomes in non-overlapping pieces (modules), which are transcribed separately and joined to a contiguous mRNA by trans-splicing. Here, we examine how many genes are encoded by Diplonema mtDNA and whether all are fragmented and their transcripts trans-spliced. Module identification is challenging due to the sequence divergence of Diplonema mitochondrial genes. By employing most sensitive protein profile search algorithms and comparing genomic with cDNA sequence, we recognize a total of 11 typical mitochondrial genes. The 10 protein-coding genes are systematically chopped up into three to 12 modules of 60–350 bp length. The corresponding mRNAs are all trans-spliced. Identification of ribosomal RNAs is most difficult. So far, we only detect the 3′-module of the large subunit ribosomal RNA (rRNA); it does not trans-splice with other pieces. The small subunit rRNA gene remains elusive. Our results open new intriguing questions about the biochemistry and evolution of mitochondrial trans-splicing in Diplonema. Oxford University Press 2011-02 2010-10-08 /pmc/articles/PMC3035467/ /pubmed/20935050 http://dx.doi.org/10.1093/nar/gkq883 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genomics
Vlcek, Cestmir
Marande, William
Teijeiro, Shona
Lukeš, Julius
Burger, Gertraud
Systematically fragmented genes in a multipartite mitochondrial genome
title Systematically fragmented genes in a multipartite mitochondrial genome
title_full Systematically fragmented genes in a multipartite mitochondrial genome
title_fullStr Systematically fragmented genes in a multipartite mitochondrial genome
title_full_unstemmed Systematically fragmented genes in a multipartite mitochondrial genome
title_short Systematically fragmented genes in a multipartite mitochondrial genome
title_sort systematically fragmented genes in a multipartite mitochondrial genome
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3035467/
https://www.ncbi.nlm.nih.gov/pubmed/20935050
http://dx.doi.org/10.1093/nar/gkq883
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