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首页> 外文期刊>Plant Cell Reports >Rapid analysis ofGBSS1andVinvgenes expressed in potato tubers using microtubers produced in liquid culture medium
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Rapid analysis ofGBSS1andVinvgenes expressed in potato tubers using microtubers produced in liquid culture medium

机译:快速分析在马铃薯块茎中表达的GBSS1ANDVINVGENS使用液体培养基生产的微管

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摘要

Key message This study established a rapid method for the gene expression analysis in potato tubers. The use of microtubers would be useful for primary evaluation of tuber-expressed genes. In the development of transgenic potato or of potato with other genome modifications (e.g., genome editing or RNA-directed DNA methylation (RdDM) and so on) to improve tuber traits, analysis of the target gene is often difficult because of the long cultivation cycle (3-4 months), large areas required, numerous materials for plant cultivation, and considerable efforts needed to obtain transgenic tubers. We demonstrate here rapid and convenient analysis of gene expression in potato microtubers. Enough microtubers for expression analysis can be induced over about 4 weeks in a simple liquid medium in an Erlenmeyer flask. High-quality RNA and protein can be easily prepared from microtubers and used for northern blot, qRT-PCR, and western blot analyses without further purification. We investigated the expression of two tuber-expressed genes (GBSS1andVinv) in microtubers derived from the wild-type and from lines derived from RdDM-mediated transcriptional gene silencing. As expected, the expression of both genes was similar between microtubers and normal tubers. Furthermore, we demonstrated that microtubers can be used in western blot and confocal immunofluorescent microscopy analyses. These results suggest that expression analysis using microtubers is a convenient tool for the analysis of tuber-expressed genes such asGBSS1andVinvin potato.
机译:关键消息本研究建立了马铃薯块茎基因表达分析的快速方法。使用微管器可用于核心表达基因的初级评估。在转基因马铃薯或土豆的发展中与其他基因组修饰(例如,基因组编辑或RNA定向的DNA甲基化(RDDM)等)以改善块茎状性状,因此由于长栽培周期,靶基因的分析通常很困难(3-4个月),需要大面积,植物栽培的众多材料,以及获得转基因块茎所需的相当大的努力。我们展示了马铃薯微管中基因表达的快速方便分析。在Erlenmeyer烧瓶中的简单液体培养基中可以在约4周内诱导足够的微管。可以容易地由微管制备高质量的RNA和蛋白质,用于Northern印迹,QRT-PCR和Western印迹分析而无需进一步纯化。我们研究了在源自野生型和衍生自RDDM介导的转录基因沉默的微管中的两种块茎表达基因(GBSS1andVinv)的表达。正如预期的那样,在微管和正常块茎之间的两种基因的表达相似。此外,我们证明了微管可用于蛋白质印迹和共聚焦免疫荧光显微镜分析。这些结果表明,使用MicroTubers的表达分析是分析块茎表达基因如GBSS1Andvinvin马铃薯的方便工具。

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  • 来源
    《Plant Cell Reports》 |2020年第11期|共10页
  • 作者单位

    Natl Agr &

    Food Res Org Inst Agrobiol Sci Kannondai 3-1-3 Tsukuba Ibaraki 3058604 Japan;

    Hirosaki Univ Fac Agr &

    Life Sci Bunkyo Ku Hirosaki Aomori 0368561 Japan;

    Natl Agr &

    Food Res Org Inst Agrobiol Sci Kannondai 3-1-3 Tsukuba Ibaraki 3058604 Japan;

    Natl Agr &

    Food Res Org Inst Agrobiol Sci Kannondai 3-1-3 Tsukuba Ibaraki 3058604 Japan;

    Calbee Potato Inc Potato Res Ctr Minami 3-2 Memuro Hokkaido 0820006 Japan;

    Calbee Potato Inc Potato Res Ctr Minami 3-2 Memuro Hokkaido 0820006 Japan;

    Matsutani Chem Ind Co Ltd Res &

    Dev Dept 2 Kita Itami 5-3 Itami Hyogo 6648508 Japan;

    Matsutani Chem Ind Co Ltd Res &

    Dev Dept 2 Kita Itami 5-3 Itami Hyogo 6648508 Japan;

    Matsutani Chem Ind Co Ltd Res &

    Dev Dept 2 Kita Itami 5-3 Itami Hyogo 6648508 Japan;

    Hirosaki Univ Fac Agr &

    Life Sci Bunkyo Ku Hirosaki Aomori 0368561 Japan;

    Hirosaki Univ Fac Agr &

    Life Sci Bunkyo Ku Hirosaki Aomori 0368561 Japan;

    Hirosaki Univ Fac Agr &

    Life Sci Bunkyo Ku Hirosaki Aomori 0368561 Japan;

    Hirosaki Univ Fac Agr &

    Life Sci Bunkyo Ku Hirosaki Aomori 0368561 Japan;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 植物细胞学;
  • 关键词

    Expression analysis; Microtuber; Solanum tuberosumL; New plant breeding techniques; Transgenic potato;

    机译:表达分析;Microotuber;solanum tuberosuml;新植物育种技术;转基因马铃薯;

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