Studies on genetic variability in male fertility restorer lines of sunflower (Helianthus annuus L. ) using molecular markers
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Title |
Studies on genetic variability in male fertility restorer lines of sunflower (Helianthus annuus L. ) using molecular markers
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Creator |
Neyol, Esha
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Contributor |
Boora, K.S.
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Subject |
Genetic variability, Helianthus annuus, Molecular markers, Male fertility restoration
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Description |
Sunflower is currently one of the most important oil producing crops in large parts of the worlds. Cytoplasmic Male Sterility (CMS) and genetic fertility restoration have been used for commercial production of hybrids. The present study was conducted to estimate genetic variability among thirty three male fertility restorer lines of sunflower. DNA extraction protocol and PCR amplification condition were standardized with required modifications. As a result, the highest quantity of DNA was extracted form AK-l-R (2545μg/ml) whereas the genotypes RHA-298 yielded lowest quantity of DNA (6825μg/ml). Agarose gel electro-phoresis and U.V. spectropholometer were used to test quality of DNA. The DNA samples were of good quality and the ratio of absorbance ranged from 1.74-1.96. For the optimum amplification of DNA in PCR 100ng genomic DNA, 3U of Taq DNA Poly., 1.5mM MgCl2, 1mM dNTPs, 1ml of 10X Taq DNA poly reaction buffer, 10um of primer and 400C annealing temperature were used. Out of thirty randum primers screened, twenty two produced amplification while eight produced no amplification. All twenty two premiers showed polymorphism among different genotypes. A total of sixty four amplified products were obtained and all were polymorphic. For all the genotypes evaluated, 1-6 bands were obtained with an average of 2.90 per primer. All the genotypes were distinguishable with combination of polymorphic bands produced by various primers. Estimates of genetic similarity based on Nei and Li equation ranged from five per cent to forty seven per cent indicating very high genetic variability among the male fertility restorer lines of sunflower. Based on cluster analysis using UPGMA, all genotypes could be divided into tow clusters. One cluster contained two genotypes (HB-375 and NDR-1) and second cluster had rest thirty one lines. Second cluster was further divided into two sub-clusters, comprising eighteen and thirteen genotypes each. These results indicate that RAPDs can be used for identification and discrimination of male fertility restorer lines of sunflower. These highly diverse lines may be further used for production of hybrids of sunflower. |
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Date |
2016-11-29T14:52:43Z
2016-11-29T14:52:43Z 2005 |
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Type |
Thesis
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Identifier |
http://krishikosh.egranth.ac.in/handle/1/88165
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Language |
en
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Format |
application/pdf
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Publisher |
CCSHAU
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