Kusunoki Kazutaka, Nakano Yuki, Tanaka Keisuke, Sakata Yoichi, Koyama Hiroyuki, Kobayashi Yuriko
Applied Biological Sciences, Gifu University, 1-1 Yanagido, Gifu, 501-1193, Japan.
NODAI Genome Research Center, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo, 156-8502, Japan.
Plant Cell Environ. 2017 Feb;40(2):249-263. doi: 10.1111/pce.12866. Epub 2017 Jan 4.
Differences in the expression levels of aluminium (Al) tolerance genes are a known determinant of Al tolerance among plant varieties. We combined transcriptomic analysis of six Arabidopsis thaliana accessions with contrasting Al tolerance and a reverse genetic approach to identify Al-tolerance genes responsible for differences in Al tolerance between accession groups. Gene expression variation increased in the signal transduction process under Al stress and in growth-related processes in the absence of stress. Co-expression analysis and promoter single nucleotide polymorphism searching suggested that both trans-acting polymorphisms of Al signal transduction pathway and cis-acting polymorphisms in the promoter sequences caused the variations in gene expression associated with Al tolerance. Compared with the wild type, Al sensitivity increased in T-DNA knockout (KO) lines for five genes, including TARGET OF AVRB OPERATION1 (TAO1) and an unannotated gene (At5g22530). These were identified from 53 Al-inducible genes showing significantly higher expression in tolerant accessions than in sensitive accessions. These results indicate that the difference in transcriptional signalling is partly associated with the natural variation in Al tolerance in Arabidopsis. Our study also demonstrates the feasibility of comparative transcriptome analysis by using natural genetic variation for the identification of genes responsible for Al stress tolerance.
铝(Al)耐受性基因表达水平的差异是植物品种间铝耐受性的一个已知决定因素。我们将六个具有不同铝耐受性的拟南芥生态型的转录组分析与反向遗传学方法相结合,以鉴定导致生态型组间铝耐受性差异的铝耐受性基因。在铝胁迫下的信号转导过程以及在无胁迫条件下的生长相关过程中,基因表达变异增加。共表达分析和启动子单核苷酸多态性搜索表明,铝信号转导途径的反式作用多态性和启动子序列中的顺式作用多态性均导致了与铝耐受性相关的基因表达变异。与野生型相比,包括AVRB作用靶点1(TAO1)和一个未注释基因(At5g22530)在内的五个基因的T-DNA敲除(KO)系中铝敏感性增加。这些基因是从53个铝诱导基因中鉴定出来的,这些基因在耐受性生态型中的表达明显高于敏感性生态型。这些结果表明,转录信号的差异部分与拟南芥铝耐受性的自然变异有关。我们的研究还证明了利用自然遗传变异进行比较转录组分析以鉴定负责铝胁迫耐受性的基因的可行性。