Analysis of genetic factors influencing the developmental rate of globally important CIMMYT wheat cultivars
Material type: ArticleLanguage: English Publication details: USA : CSSA : Wiley, 2005.ISSN:- 1435-0653 (Online)
- 0011-183X
Item type | Current library | Collection | Call number | Copy number | Status | Date due | Barcode | Item holds | |
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Article | CIMMYT Knowledge Center: John Woolston Library | CIMMYT Staff Publications Collection | CIS-4554 (Browse shelf(Opens below)) | 1 | Available | 633364 |
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Peer review
Peer-review: Yes - Open Access: Yes|http://science.thomsonreuters.com/cgi-bin/jrnlst/jlresults.cgi?PC=MASTER&ISSN=0011-183X
The rate at which wheat (Triticum aestivum L.) reaches anthesis and other developmental stages depends largely on the variation of three major factors: vernalization (Vrn), photoperiod (Ppd), and earliness per se (Eps). The objectives of this study were to characterize a set of genotypes for the presence of developmental genes and their potential association to adaptability and to identify diagnostic molecular markers for the vernalization gene Vrn-D1. Fifty-one genotypes were crossed with testers containing known Vrn and Ppd genes. To determine earliness per se and its interaction with temperature, genotypes were vernalized for 8 wk and placed in a 24-h photoperiod regime at two temperatures. To validate molecular markers for Vrn-D1, the cultivars were genotyped with closely linked SSR markers Xgwm292-5D and Xgwm212-5D. Segregation analysis on F2 populations of field-grown plants showed that Vrn-D1 was present in 66% of the cultivars, while Vrn-A1, Vrn-B1, and Vrn4 were found in 41, 39, and 8% of the lines, respectively, either solely or in combination with other Vrn genes. A low percentage of cultivars appeared to have a constitutive genetic character for early flowering (Eps), while most of the cultivars may have temperature-sensitive genes that respond to local environmental changes. Vrn-D1 was reliably detected in 76.5% of the genotypes using the 215-bp allele of microsatellite marker Xgwm292-5D, whereas Xgwm212-5D did not reveal sufficient allelic variation within the tested wheats.
Genetic Resources Program
Text in English
Crop Science Society of America (CSSA)|0009
CCJL01