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Comparative study of transcriptional and physiological responses to salinity stress in two contrasting Populus alba L. genotypes

机译:两种相反的白杨基因型对盐分胁迫的转录和生理响应的比较研究

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摘要

Soil salinity is an important limiting factor to tree growth and productivity. Populus alba L. is a moderately salt-tolerant species and its natural populations are adapted to contrasting environments, thus providing genetic resources to identify key genes for tolerance to abiotic stress, such as salinity. To elucidate the molecular and genetic basis of variation for salinity tolerance in P. alba, we analyzed the short-term ecophysiological and transcriptome response to salinity. Two contrasting genotypes, 6K3, salt sensitive, and 14P11, salt tolerant, originating from North and South Italy, respectively, were challenged with salt stress (200 mM NaCl). Sodium accumulated in the leaves of salt-treated plants and its concentration increased with time. The net photosynthesis was strongly reduced by salinity in both genotypes, with 6K3 being significantly more affected than 14P11. The transcriptional changes in leaves were analyzed using cDNA microarrays containing about 7000 stress-related poplar expressed sequence tags (EST). A microarray experiment based on RNA pooling showed a number of salinity-­regulated transcripts that markedly increased from 3 h to 3 days of salinity treatment. Thus, a detailed analysis was performed on replicated plants collected at 3 days, when ∼20% of transcripts showed significant change induced by salinity. In 6K3, there were more genes with decreased expression than genes with increased expression, whereas such a difference was not found in 14P11. Most transcripts with decreased expression were shared between the two genotypes, whereas transcripts with increased expression were mostly regulated in a genotype-specific manner. The commonly decreased transcripts (71 genes) were functionally related to carbohydrate metabolism, energy metabolism and photosynthesis. These biological processes were consistent with the strong inhibition of photosynthesis, caused by salinity. The commonly increased transcripts (13 genes) were functionally related to primary metabolism and biosynthesis of proteins and macromolecules. The salinity-increased transcripts discriminated the molecular response of the two genotypes. In 14P11, the 21 genes specifically salinity-induced were related to stress response, cell development, cell death and catabolism. In 6K3, the 15 genes with salinity-increased expression were involved in protein biosynthesis, metabolism of macromolecules and cell organization and biogenesis. The difference in transcriptome response between the two genotypes could address the molecular basis of intra-specific variation of salinity tolerance in P. alba.
机译:土壤盐分是限制树木生长和生产力的重要限制因素。白杨(Populus alba L.)是一种中度耐盐物种,其自然种群适应不同的环境,因此提供了遗传资源来鉴定耐盐胁迫等非生物胁迫的关键基因。为了阐明白纹病菌耐盐性变异的分子和遗传基础,我们分析了对盐度的短期生态生理和转录组反应。分别来自意大利北部和南部的两个相反的基因型,分别对盐敏感的6​​K3和耐盐的14P11,受到盐胁迫(200 mM NaCl)的攻击。钠在盐处理过的植物的叶子中积累,其浓度随时间增加。两种基因型的盐度都极大地降低了净光合作用,其中6K3的影响明显大于14P11。使用含有约7000个应激相关杨树表达序列标签(EST)的cDNA微阵列分析了叶片中的转录变化。基于RNA汇集的微阵列实验显示,许多盐度调节的转录物从盐度处理的3小时到3天明显增加。因此,当大约20%的转录本显示出盐度引起的显着变化时,对在第3天收集的复制植物进行了详细分析。在6K3中,表达减少的基因多于表达增加的基因,而在14P11中未发现这种差异。在两种基因型之间共享大多数表达降低的转录本,而表达增强的转录本大多以基因型特异性的方式进行调控。通常减少的转录本(71个基因)在功能上与碳水化合物代谢,能量代谢和光合作用有关。这些生物过程与盐度引起的对光合作用的强抑制作用是一致的。通常增加的转录本(13个基因)在功能上与蛋白质和大分子的初级代谢和生物合成有关。盐度增加的转录本区分了两种基因型的分子反应。在14P11中,特别是盐分诱导的21个基因与应激反应,细胞发育,细胞死亡和分解代谢有关。在6K3中,盐度表达增加的15个基因参与了蛋白质的生物合成,大分子的代谢以及细胞的组织和生物发生。两种基因型之间转录组反应的差异可以解决白纹病菌耐盐性种内变异的分子基础。

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  • 来源
    《Tree Physiology》 |2011年第12期|p.1335-1355|共21页
  • 作者单位

    Department for Innovation in Biological, Agro-Food and Forest Systems (DIBAF), University of Tuscia, Via S. Camillo de Lellis, 01100 Viterbo, Italy;

    Department for Innovation in Biological, Agro-Food and Forest Systems (DIBAF), University of Tuscia, Via S. Camillo de Lellis, 01100 Viterbo, Italy;

    CASPUR, Consorzio interuniversitario per le applicazioni di supercalcolo per università e ricerca, Via dei Tizii 6, 00185, Roma, Italy;

    Department of Biosciences, Division of Plant Biology, University of Helsinki, Viikinkaari 1 (PL 65) 00014 Helsinki, Finland;

    Department for Innovation in Biological, Agro-Food and Forest Systems (DIBAF), University of Tuscia, Via S. Camillo de Lellis, 01100 Viterbo, Italy;

    Institute of Biotechnology, University of Helsinki, 00014 Helsinki, Finland;

    Department for Innovation in Biological, Agro-Food and Forest Systems (DIBAF), University of Tuscia, Via S. Camillo de Lellis, 01100 Viterbo, Italy;

    Department for Innovation in Biological, Agro-Food and Forest Systems (DIBAF), University of Tuscia, Via S. Camillo de Lellis, 01100 Viterbo, Italy;

    Plant Protection Institute (CNR-IPP), National Research Council, Via Madonna del Piano, 10 50019 Sesto Fiorentino, Firenze, Italy;

    Plant Protection Institute (CNR-IPP), National Research Council, Via Madonna del Piano, 10 50019 Sesto Fiorentino, Firenze, Italy;

    Institute of Biotechnology, University of Helsinki, 00014 Helsinki, Finland;

    Department of Agronomy, Forestry and Land Use (DAF), Agricultural Research Council (CRA), Via del Caravita 7/a, 00186 Roma, Italy;

    Department for Innovation in Biological, Agro-Food and Forest Systems (DIBAF), University of Tuscia, Via S. Camillo de Lellis, 01100 Viterbo, Italy;

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