DNA sequences of fatty acid elongase 1 genes FAE1.1 (EA) and FAE1.2 (Ec) were isolated and characterized for 30 com- mercialized low erucic acid rapeseed (LEAR) cultivars in China. Four types of independent muta...DNA sequences of fatty acid elongase 1 genes FAE1.1 (EA) and FAE1.2 (Ec) were isolated and characterized for 30 com- mercialized low erucic acid rapeseed (LEAR) cultivars in China. Four types of independent mutation leading to low erucic acid trait were found, i.e., a single-base transition (eAl), a two-base deletion (ec2) and four-base deletion (eC4) as well as single-base transition with a four-base deletion (eA.). Three genotypes, i.e., eA1eA1eC2eC2, eA1eA1eC4eC4 and eA.eA.ec4ec4 were responsible for LEA content in storage Iipids of different rapeseed cultivars. Most of the LEAR cultivars had a genotype of eA1eA1ec2ec2, which were descended from the first LEAR cultivar, Oro. Yeast expression analysis revealed that two-base-pair (AA) deletion (ec2) at the base sites of 1 422-1 423 in the C genome FAE1 gene resulted in the absence of the condensing enzyme and led to the failure to produce erucic acid. Coexpression of FAE1 and ketoacyI-CoA reductase (KCR) or enoyI-CoA reductase (ECR) was found in high erucic acid rapeseed (HEAR) but not in LEAR (eA1eA1ec2ec2oreA1eA1ec4ec4). Moreover, KCR and ECR were still coordinately regulated in eA1eA1ec2ec2 or eA1eA1ec4ec4 genotypes, suggesting that the expression of two genes was tightly linked. In addition, specific detection methods were developed by high-resolution melting curve analysis in order to detect eA1 and ec4.展开更多
基金financially supported by the National Natural Science Foundation of China (30471099)the National High Technology and Development Program of China (2006AA10A113)
文摘DNA sequences of fatty acid elongase 1 genes FAE1.1 (EA) and FAE1.2 (Ec) were isolated and characterized for 30 com- mercialized low erucic acid rapeseed (LEAR) cultivars in China. Four types of independent mutation leading to low erucic acid trait were found, i.e., a single-base transition (eAl), a two-base deletion (ec2) and four-base deletion (eC4) as well as single-base transition with a four-base deletion (eA.). Three genotypes, i.e., eA1eA1eC2eC2, eA1eA1eC4eC4 and eA.eA.ec4ec4 were responsible for LEA content in storage Iipids of different rapeseed cultivars. Most of the LEAR cultivars had a genotype of eA1eA1ec2ec2, which were descended from the first LEAR cultivar, Oro. Yeast expression analysis revealed that two-base-pair (AA) deletion (ec2) at the base sites of 1 422-1 423 in the C genome FAE1 gene resulted in the absence of the condensing enzyme and led to the failure to produce erucic acid. Coexpression of FAE1 and ketoacyI-CoA reductase (KCR) or enoyI-CoA reductase (ECR) was found in high erucic acid rapeseed (HEAR) but not in LEAR (eA1eA1ec2ec2oreA1eA1ec4ec4). Moreover, KCR and ECR were still coordinately regulated in eA1eA1ec2ec2 or eA1eA1ec4ec4 genotypes, suggesting that the expression of two genes was tightly linked. In addition, specific detection methods were developed by high-resolution melting curve analysis in order to detect eA1 and ec4.