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Analysis of Ac/Ds Activation Tagged Mutants in Tomato (Solanum lycopersicum)

机译:番茄中Ac / Ds活化标记突变体的分析

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摘要

Tomato (Solanum lycopersicum) is a crop of immense economic and nutritional importance worldwide and also a good model organism for genomic studies of other dicot species. The recent completion of the tomato genome sequence is a great milestone towards learning about the tomato genome. Elucidation of the function of the different genes using different functional genomic tools is therefore important in adding to this resource. To this end, we have developed an Ac-Ds transposon 'activation tagging' (ATag) system to be able to transpose transposon inserts, bearing a strong 35S-enhancer element, all around the genome. An Ac-Ds ATag construct was used to generate transformants in the tomato cultivar M82 that has an erect determinate habit, suitable for greenhouse and field screening. The progeny of putative tomato transformants were germinated and grown to maturity in the greenhouse. Plants with obvious mutant phenotypes were identified, which included dwarfism, altered leaf morphology and necrotic spots on leaves. Presence of the ATag transformed construct was confirmed in the plants by genomic PCR using primers specific to different parts of the Ac/Ds cassette. Activity of the transposon system was also tested by excision PCR using primers flanking the Ds insert in the construct. Insertion sites of the Ds ATag were determined using TAIL-PCR for the progeny plants, and the tagged genes in two mutants were identified by alignment of the flanking sites to the tomato genome. With the availability of the tomato genome sequence, the mutants described will be a good resource for the identification of genes for plant development and tomato breeding.
机译:番茄(Solanum lycopersicum)是一种在全球范围内具有重要经济和营养意义的作物,也是其他双子叶植物基因组研究的良好模式生物。番茄基因组序列的最新完成是学习番茄基因组的重要里程碑。因此,使用不同的功能基因组学工具阐明不同基因的功能对于增加这种资源非常重要。为此,我们开发了一个Ac-Ds转座子“激活标签”(ATag)系统,能够在整个基因组中转座带有强大的35S增强子的转座子插入片段。 Ac-Ds ATag构建体用于在番茄栽培品种M82中产生具有直立确定习性的转化体,适用于温室和田间筛选。推定的番茄转化子的后代发芽并在温室中生长到成熟。鉴定出具有明显突变表型的植物,包括矮化,叶片形态改变和叶片坏死斑。使用对Ac / Ds盒不同部分具有特异性的引物,通过基因组PCR在植物中证实了ATag转化构建体的存在。转座子系统的活性也通过切除PCR使用构建体中Ds插入物侧翼的引物进行了测试。使用TAIL-PCR确定后代植物的Ds ATag的插入位点,并且通过将侧翼位点与番茄基因组比对来鉴定两个突变体中的标记基因。随着番茄基因组序列的可用性,所述突变体将成为鉴定用于植物发育和番茄育种的基因的良好资源。

著录项

  • 作者

    Randome, Ipeleng.;

  • 作者单位

    University of Arkansas.;

  • 授予单位 University of Arkansas.;
  • 学科 Plant sciences.;Botany.;Molecular biology.
  • 学位 M.S.
  • 年度 2015
  • 页码 74 p.
  • 总页数 74
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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