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RFLP mapping of the sugary enhancer1 gene in maize
Year:
1995
Source of publication :
Theoretical and Applied Genetics
Authors :
Tadmor, Yaakov
;
.
Volume :
91
Co-Authors:
Tadmor, Y., Department of Horticulture, University of Illinois, Urbana, 61801, IL, United States
Azanza, F., Department of Horticulture, University of Illinois, Urbana, 61801, IL, United States
Han, T., Department of Horticulture, University of Illinois, Urbana, 61801, IL, United States
Rocheford, T.R., Department of Agronomy, University of Illinois, Urbana, 61801, IL, United States
Juvik, J.A., Department of Horticulture, University of Illinois, Urbana, 61801, IL, United States
Facilitators :
From page:
489
To page:
494
(
Total pages:
6
)
Abstract:
RFLP marker data from an F2:3 population derived from a cross between a sugary1 (su1) and a sugary enhancer1 (su1, sel) inbred were used to construct a genetic linkage map of maize. This map includes 93 segregating marker loci distributed throughout the maize genome, providing a saturated linkage map that is suitable for linkage analysis with quantitative trait loci (QTL). This population, which has been immortalized in the form of sibbed F2:3 families, was derived from each of the 214 F2 plants and along with probe data are available to the scientific community. QTL analysis for kernel sucrose (the primary form of sugar) concentration at 20 days after pollination (DAP) uncovered the segregation of seven major QTL influencing sucrose concentration; a locus linked to umc36a described the greatest proportion of the variation (24.7%). Since maltose concentration has previously been reported to be associated with the se1 phenotype, an analysis of probe associations with maltose concentration at 40 DAP was also conducted. The highly significant association of umc36a with maltose and sucrose concentrations provided evidence that this probe is linked to se1. Phenotypic evaluation for the se1 genotype in each F2:3 family enabled us to map the gene 12.1 cM distal to umc36a. In contrast to previous work where se1 was reported to be located on chromosome four, our data strongly suggest that the sugary enhancer1 locus maps on the the distal portion of the long arm of chromosome 2 in the maize genome. © 1995 Springer-Verlag.
Note:
Related Files :
Genetics
maize
Quality
se1
sucrose
Sweet corn
Zea mays
Show More
Related Content
More details
DOI :
10.1007/BF00222978
Article number:
Affiliations:
Database:
Scopus
Publication Type:
article
;
.
Language:
English
Editors' remarks:
ID:
20761
Last updated date:
02/03/2022 17:27
Creation date:
16/04/2018 23:38
Scientific Publication
RFLP mapping of the sugary enhancer1 gene in maize
91
Tadmor, Y., Department of Horticulture, University of Illinois, Urbana, 61801, IL, United States
Azanza, F., Department of Horticulture, University of Illinois, Urbana, 61801, IL, United States
Han, T., Department of Horticulture, University of Illinois, Urbana, 61801, IL, United States
Rocheford, T.R., Department of Agronomy, University of Illinois, Urbana, 61801, IL, United States
Juvik, J.A., Department of Horticulture, University of Illinois, Urbana, 61801, IL, United States
RFLP mapping of the sugary enhancer1 gene in maize
RFLP marker data from an F2:3 population derived from a cross between a sugary1 (su1) and a sugary enhancer1 (su1, sel) inbred were used to construct a genetic linkage map of maize. This map includes 93 segregating marker loci distributed throughout the maize genome, providing a saturated linkage map that is suitable for linkage analysis with quantitative trait loci (QTL). This population, which has been immortalized in the form of sibbed F2:3 families, was derived from each of the 214 F2 plants and along with probe data are available to the scientific community. QTL analysis for kernel sucrose (the primary form of sugar) concentration at 20 days after pollination (DAP) uncovered the segregation of seven major QTL influencing sucrose concentration; a locus linked to umc36a described the greatest proportion of the variation (24.7%). Since maltose concentration has previously been reported to be associated with the se1 phenotype, an analysis of probe associations with maltose concentration at 40 DAP was also conducted. The highly significant association of umc36a with maltose and sucrose concentrations provided evidence that this probe is linked to se1. Phenotypic evaluation for the se1 genotype in each F2:3 family enabled us to map the gene 12.1 cM distal to umc36a. In contrast to previous work where se1 was reported to be located on chromosome four, our data strongly suggest that the sugary enhancer1 locus maps on the the distal portion of the long arm of chromosome 2 in the maize genome. © 1995 Springer-Verlag.
Scientific Publication
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