Quantification of dominance for proteins pleiotropically affected by opaque-2 in maize
The maize opaque-2 (o2) mutation is known to have numerous pleiotropic effects. Using two different genetic backgrounds, endosperm proteins from isogenic lines of the o2 locus and their reciprocal hybrids were compared by high-resolution two-dimensional electrophoresis (2-D PAGE), and the 2-D gels s...
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Published in: | Heredity Vol. 70; no. 1; pp. 38 - 51 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
Basingstoke
Nature Publishing
1993
Nature Publishing Group |
Subjects: | |
Online Access: | Get full text |
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Summary: | The maize opaque-2 (o2) mutation is known to have numerous pleiotropic effects. Using two different genetic backgrounds, endosperm proteins from isogenic lines of the o2 locus and their reciprocal hybrids were compared by high-resolution two-dimensional electrophoresis (2-D PAGE), and the 2-D gels stained with Coomassie blue or silver were analysed using a computer-assisted system for quantification of polypeptide spots. The aim of this work was (i) to identify polypeptides, the amount of which is affected by the single gene substitution, and (ii) to assess the dominance relations for every affected polypeptide. This is an example where pleiotropically related characters display different inheritance, which could generate heterozygous phenotypes with original properties as compared to their homozygous parents. Because O2 belongs to the basic region-leucine zipper family of transcription activators, our results show that 2-D PAGE of isogenic lines represents a straightforward method to identify gene products affected by a transcription factor, whether they are products of its target genes, or products indirectly affected by far-reaching effects. This is a prerequisite to understanding the multiple molecular and physiological consequences of the action of such factors. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0018-067X 1365-2540 0018-067X |
DOI: | 10.1038/hdy.1993.6 |