4.8 Article

Systematically fragmented genes in a multipartite mitochondrial genome

期刊

NUCLEIC ACIDS RESEARCH
卷 39, 期 3, 页码 979-988

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkq883

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资金

  1. Canadian Institute for Health Research [MOP-79309]
  2. Czech Ministry of Education, Youth and Sports [1M0520, 6007665801]
  3. Grant Agency of the Czech Republic [204/09/1667]
  4. Premium Academiae award

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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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