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向日葵中脱水素基因的序列变异性

Sequence variability of a dehydrin gene within Helianthus annuus.

作者信息

Natali L, Giordani T, Cavallini A

机构信息

Department of Agricultural Plant Biology, Genetics Section, Via Matteotti 1/B, I-56124 Pisa, Italy.

出版信息

Theor Appl Genet. 2003 Mar;106(5):811-8. doi: 10.1007/s00122-002-1093-z. Epub 2002 Oct 31.

Abstract

Dehydrins are proteins produced during the late stages of plant embryo development and following any environmental stimulus involving dehydration. In order to investigate the variability of a dehydrin-encoding gene (Dhn1) in cultivated and wild sunflower (Helianthus annuus) genotypes, near-complete alleles were isolated by the polymerase chain reaction and sequenced. All of the isolated sequences were found to contain the typical dehydrin domains, and interrupted by an intron. The number of nucleotide substitutions and indels per site was calculated. With respect to the overall sequence, variation in both the coding and noncoding [intron and 3'-UTR (untranslated region)] sequences was much larger among wild accessions than among cultivars. No variation was observed in 3'-UTRs from cultivated sunflowers. Different coding regions showed a different numbers of synonymous and nonsynonymous substitutions. The Y and K domains were the most conserved in both wild and cultivated genotypes. Sequence analysis of the deduced dehydrin proteins showed that nucleotide substitutions in wild accessions should also determine large biochemical differences at the protein level. All of the isolated alleles were however functional, at least at the transcription level. To our knowledge these are the first data on intraspecific genetic variability of such a stress response gene. The low variability of dehydrin genes from cultivated sunflower is discussed in relation to the origin of sunflower cultivars. The possibility of rescuing general genetic variability through crosses to wild accessions of H. annuus rather than using wild Helianthus species is also discussed.

摘要

脱水素是在植物胚胎发育后期以及任何涉及脱水的环境刺激后产生的蛋白质。为了研究栽培和野生向日葵(向日葵)基因型中脱水素编码基因(Dhn1)的变异性,通过聚合酶链反应分离了近完整的等位基因并进行测序。所有分离的序列都含有典型的脱水素结构域,并被一个内含子打断。计算了每个位点的核苷酸替换和插入缺失的数量。就整个序列而言,野生材料中编码和非编码[内含子和3'-UTR(非翻译区)]序列的变异比栽培品种中要大得多。在栽培向日葵的3'-UTR中未观察到变异。不同的编码区域显示出不同数量的同义替换和非同义替换。Y和K结构域在野生和栽培基因型中都是最保守的。推导的脱水素蛋白的序列分析表明,野生材料中的核苷酸替换也应该在蛋白质水平上决定较大的生化差异。然而,所有分离的等位基因至少在转录水平上是有功能的。据我们所知,这些是关于这种应激反应基因种内遗传变异性的首批数据。结合向日葵栽培品种的起源,讨论了栽培向日葵脱水素基因低变异性的问题。还讨论了通过与野生向日葵杂交而不是使用野生向日葵物种来拯救一般遗传变异性的可能性。

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