ArticleMolecular & general genetics : MGG1995
Pulsed-field gel mapping of maize mitochondrial chromosomes.
Article in Molecular & general genetics : MGG, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 24 citations in OpenAlex.
- Characterization of the structure and DNA complexity of mung bean mitochondrial nucleoids.Molecules and cells · 2011Article
- Flow cytometric analysis of mitochondrial populations in HL-CMS systems of rice under H2O2 stress.Protoplasma · 2010Article
- Flow cytometric identification of two different rhodamine-123-stained mitochondrial populations in maize leaves.Protoplasma · 2007Article
- Structural and functional characterizations of mung bean mitochondrial nucleoids.Nucleic acids research · 2005Article
- The mitochondrial DNA of land plants: peculiarities in phylogenetic perspective.Current genetics · 2004Review
- High content, size and distribution of single-stranded DNA in the mitochondria of Chenopodium album (L.).Plant molecular biology · 1997Article
- Electron microscopic investigation of mitochondrial DNA from Chenopodium album (L.).Current genetics · 1996Article
- Size and Structure of Replicating Mitochondrial DNA in Cultured Tobacco Cells.The Plant cell · 1996Article
- Investigation of plant organellar DNAs by pulsed-field gel electrophoresis.Current genetics · 1995Article
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Authors and funding
2 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pulsed-field gel electrophoresis (PFGE) in combination with infrequently cutting restriction enzymes was used to investigate the structure of the mitochondrial (mt) genome of the maize variety Black Mexican Sweet (BMS). The mt genome of this variety was found to resemble that of the closely related B37N variety, with one recombination and five insertion/deletion events being sufficient to account for the differences observed between the two genomes. The majority of the BMS genome is organized as a number of subgenomic chromosomes with circular restriction maps. Several large repeated sequences are found in the BMS mt genome, but not all appear to be in recombinational equilibrium. No molecules large enough to contain the entire mt genome were discernible using these techniques. The mapping approach described here provides a means of quickly analyzing the large and complex mt genomes of plants.
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