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The maize NCS2 abnormal growth mutant has a chimeric nad4-nad7 mitochondrial gene and is associated with reduced complex I function.
Marienfeld, J R; Newton, K J.
Affiliation
  • Marienfeld JR; Division of Biological Sciences, University of Missouri, Columbia 65211.
Genetics ; 138(3): 855-63, 1994 Nov.
Article in En | MEDLINE | ID: mdl-7851780
ABSTRACT
The molecular basis of the maternally inherited, heteroplasmic NCS2 mutant of maize was investigated. Analysis of the NCS2 mtDNA showed that it closely resembles the progenitor cmsT mitochondrial genome, except that the mutant genome contains a fused nad4-nad7 gene and is deleted for the small fourth exon of nad4. The rearrangement has occurred at a 16-bp repeat present in the third intron of the nad4 gene and in the second intron of the nad7 gene. Transcripts containing exon 4 of the nad4 gene are greatly reduced in mtRNA preparations from heteroplasmic NCS2 plants; larger transcripts are associated with the first three nad4 exons. Identical 5' ends of the nad4 transcripts have been mapped 396 and 247 bp upstream of the start codon in mtRNAs from both NCS2 and related non-NCS plants. The putative transcription termination signal of nad4 is deleted in mutant DNA, resulting in the production of the unique longer transcripts. The complex transcript pattern associated with nad7 is also altered in the mutant. Both nad4 and nad7 encode subunits of complex I (NADH dehydrogenase) of the mitochondrial electron transfer chain. Oxygen uptake experiments show that the functioning of complex I is specifically reduced in mitochondria isolated from NCS2 mutant plants.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / NAD(P)H Dehydrogenase (Quinone) / Genes, Plant / Zea mays Type of study: Risk_factors_studies Language: En Journal: Genetics Year: 1994 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / NAD(P)H Dehydrogenase (Quinone) / Genes, Plant / Zea mays Type of study: Risk_factors_studies Language: En Journal: Genetics Year: 1994 Document type: Article