Organization and Expression of the Mitochondrial Genome in the Nicotiana sylvestris CMSII Mutant
Author(s) -
Christine Lelandais,
Béatrice Albert,
Sophie Gutierres,
Rosine De Paepe,
Bernard Godelle,
F. Vedel,
Philippe Chétrit
Publication year - 1998
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1093/genetics/150.2.873
Subject(s) - biology , mitochondrial dna , genetics , genome , gene , mutant , cosmid , nuclear gene , microbiology and biotechnology
Previous analyses suggested that the Nicotiana sylvestris CMSII mutant carried a large deletion in its mitochondrial genome. Here, we show by cosmid mapping that the deletion is 60 kb in length and contains several mitochondrial genes or ORFs, including the complex I nad7 gene. However, due to the presence of large duplications in the progenitor mitochondrial genome, the only unique gene that appears to be deleted is nad7. RNA gel blot data confirm the absence of nad7 expression, strongly suggesting that the molecular basis for the CMSII abnormal phenotype, poor growth and male sterility, is the altered complex I structure. The CMSII mitochondrial genome appears to consist essentially of one of two subgenomes resulting from recombination between direct short repeats. In the progenitor mitochondrial genome both recombination products are detected by PCR and, reciprocally, the parental fragments are detected at the substoichiometric level in the mutant. The CMSII mtDNA organization has been maintained through six sexual generations.
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