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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...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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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. |
format | Text |
id | pubmed-3035467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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