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Natural variation for seed dormancy in Arabidopsis is regulated by additive genetic and molecular pathways

机译:拟南芥种子休眠的自然变异受累加的遗传和分子途径调控

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摘要

Timing of germination is presumably under strong natural selection as it determines the environmental conditions in which a plant germinates and initiates its postembryonic life cycle. To investigate how seed dormancy is controlled, quantitative trait loci (QTL) analyses has been performed in six Arabidopsis thaliana recombinant inbred line populations by analyzing them simultaneously using a mixed model QTL approach. The recombinant inbred line populations were derived from crosses between the reference accession Lands-berg erecta (Ler) and accessions from different world regions. In total, 11 delay of germination (DOG) QTL have been identified, and nine of them have been confirmed by near isogenic lines (NILs). The absence of strong epistatic interactions between the different DOG loci suggests that they affect dormancy mainly by distinct genetic pathways. This was confirmed by analyzing the transcriptome of freshly harvested dry seeds of five different DOG NILs. All five DOG NILs showed discernible and different expression patterns compared with the expression of their genetic background Ler. The genes identified in the different DOG NILs represent largely different gene ontology profiles. It is proposed that natural variation for seed dormancy in Arabidopsis is mainly controlled by different additive genetic and molecular pathways rather than epistatic interactions, indicating the involvement of several independent pathways.
机译:萌发的时机大概是在强烈的自然选择下确定的,因为它决定了植物萌发并启动其胚后生命周期的环境条件。为了研究如何控制种子休眠,已经通过使用混合模型QTL方法同时分析了六个拟南芥重组自交系种群,对数量性状基因座(QTL)进行了分析。重组自交系种群来自参考种地Lands-berg erecta(Ler)与世界不同地区的种之间的杂交。总共确定了11个发芽延迟(DOG)QTL,其中9个已通过近等基因系(NIL)确认。不同的DOG基因座之间缺乏强烈的上位性相互作用,表明它们主要通过独特的遗传途径影响休眠。通过分析五个不同的DOG NIL的新鲜收获的干种子的转录组可以证实这一点。与它们的遗传背景Ler的表达相比,所有五个DOG NIL均显示出可识别且不同的表达模式。在不同的DOG NIL中鉴定出的基因代表了完全不同的基因本体概貌。拟南芥种子休眠的自然变异主要由不同的加性遗传和分子途径而不是上位性相互作用控制,这表明参与了几种独立的途径。

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  • 作者单位

    Department of Molecular Plant Physiology, Utrecht University, 3584 CH Utrecht, The Netherlands Laboratory of Genetics, Wageningen University, 6708 PB Wageningen, The Netherlands;

    Department of Molecular Plant Physiology, Utrecht University, 3584 CH Utrecht, The Netherlands Centre for BioSystems Genomics, 6700 AB Wageningen, The Netherlands;

    Laboratory of Genetics, Wageningen University, 6708 PB Wageningen, The Netherlands;

    Laboratory of Genetics, Wageningen University, 6708 PB Wageningen, The Netherlands;

    Biometris-Applied Statistics, Wageningen University and Research Centre, 6708 PB Wageningen, The Netherlands;

    Centre for BioSystems Genomics, 6700 AB Wageningen, The Netherlands Biometris-Applied Statistics, Wageningen University and Research Centre, 6708 PB Wageningen, The Netherlands;

    Laboratory of Genetics, Wageningen University, 6708 PB Wageningen, The Netherlands;

    Department of Plant Molecular Genetics, Centra Nacional de Biotecnologia (CNB) and Consejo Superior de Investigaqones Cientificas (CSIC), E-28049 Madrid, Spain;

    Department of Plant Molecular Genetics, Centra Nacional de Biotecnologia (CNB) and Consejo Superior de Investigaqones Cientificas (CSIC), E-28049 Madrid, Spain;

    Max Planck Institute for Plant Breeding Research, 50829 Cologne, Germany;

    Centre for BioSystems Genomics, 6700 AB Wageningen, The Netherlands Biometris-Applied Statistics, Wageningen University and Research Centre, 6708 PB Wageningen, The Netherlands;

    Department of Molecular Plant Physiology, Utrecht University, 3584 CH Utrecht, The Netherlands Centre for BioSystems Genomics, 6700 AB Wageningen, The Netherlands;

    Laboratory of Genetics, Wageningen University, 6708 PB Wageningen, The Netherlands Max Planck Institute for Plant Breeding Research, 50829 Cologne, Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    recombinant inbred lines; quantitative trait loci analyses; near isogenic lines; transcriptome analyses;

    机译:重组自交系;数量性状位点分析;等基因线附近;转录组分析;

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