首页> 外文期刊>Journal of Plant Biochemistry and Biotechnology >Sequence variation in 3'UTR region of crtRB1 gene and its effect on beta-carotene accumulation in maize kernel.
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Sequence variation in 3'UTR region of crtRB1 gene and its effect on beta-carotene accumulation in maize kernel.

机译:crtRB1基因3'UTR区域的序列变异及其对玉米籽粒中β-胡萝卜素积累的影响。

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beta-carotene fortification of maize has emerged as a potential, long-term and sustainable approach to alleviate vitamin A deficiency in humans. Among the several genes involved in the carotenoid biosynthetic pathway, the 543 bp allele at crtRB1 3'TE (Transposable Element) gene (allele 1, without insertion) is associated with higher beta-carotene accumulation. Estimation of beta-carotene through high performance liquid chromatography showed that the CIMMYT genotypes with allele 1 had high kernel beta-carotene content whereas the Indian inbreds with the same allele had low beta-carotene content. To know the reason for this variation, allele 1 of crtRB1 3'TE gene was sequenced from a set of 11 diverse maize inbreds collected from CIMMYT and Indian germplasm. The sequence data of the allele 1 revealed the presence of 13 single nucleotide polymorphisms (SNPs) and 7 insertions and deletions (InDels). Exonic region had two SNPs, intronic region had one SNP and one InDel, whereas 3'-untranslated region (UTR) region of the gene showed 10 SNPs and 6 InDels. Among the several SNPs and InDels, SNP4, SNP13, InDel6 and InDel7 identified in the 3'-UTR region clearly differentiated the high and the low beta-carotene genotypes. These 3'-UTR polymorphisms in allele 1 of the crtRB1 3'TE gene could be associated with the variation in kernel beta-carotene accumulation by regulating the translation and stability of the mRNA. The SNPs and the InDels associated with higher level of beta-carotene will be used as a gene-based marker(s) in selection of genotypes and to develop biofortified maize hybrids to alleviate vitamin A deficiency in humans
机译:玉米的β-胡萝卜素强化已经成为缓解人类维生素A缺乏的潜在,长期和可持续的方法。在参与类胡萝卜素生物合成途径的几个基因中,crtRB1 3'TE(转座因子)基因(等位基因1,未插入)处的543 bp等位基因与更高的β-胡萝卜素积累有关。通过高效液相色谱法估算β-胡萝卜素表明,具有等位基因1的CIMMYT基因型具有较高的籽粒β-胡萝卜素含量,而具有相同等位基因的印度近交种具有较低的β-胡萝卜素含量。为了知道这种变异的原因,从11种从CIMMYT和印度种质中收集的玉米近交系中,对crtRB1 3'TE基因的等位基因1进行了测序。等位基因1的序列数据显示存在13个单核苷酸多态性(SNP)和7个插入和缺失(InDels)。外显子区具有两个SNP,内含子区具有一个SNP和一个InDel,而该基因的3'-非翻译区(UTR)区域显示有10个SNP和6个InDel。在几个SNP和InDel中,在3'-UTR区域中鉴定出的SNP4,SNP13,InDel6和InDel7清楚地区分了高和低β-胡萝卜素基因型。 crtRB1 3'TE基因的等位基因1中的这些3'-UTR多态性可能与通过调节mRNA的翻译和稳定性而导致内核β-胡萝卜素积累的变化有关。与更高水平的β-胡萝卜素相关的SNP和InDels将用作基因型选择的基因标记,并开发生物强化的玉米杂种以减轻人类维生素A的缺乏

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