Mohammadi Mohsen, Kav Nat N V, Deyholos Michael K
Department of Biological Sciences, University of Alberta, Edmonton, Canada T6E 2L3.
Plant Cell Environ. 2007 May;30(5):630-45. doi: 10.1111/j.1365-3040.2007.01645.x.
We used a long-oligonucleotide microarray to identify transcripts that increased or decreased in abundance in roots of dehydration-tolerant hexaploid bread wheat, in response to withholding of water. We observed that the major classes of dehydration-responsive genes (e.g. osmoprotectants, compatible solutes, proteases, glycosyltransferases/hydrolases, signal transducers components, ion transporters) were generally similar to those observed previously in other species and osmotic stresses. More specifically, we highlighted increases in transcript expression for specific genes including those putatively related to the synthesis of asparagine, trehalose, oligopeptide transporters, metal-binding proteins, the gamma-aminobutyric acid (GABA) shunt and transcription factors. Conversely, we noted a decrease in transcript abundance for diverse classes of glutathione and sulphur-related enzymes, specific amino acids, as well as MATE-efflux carrier proteins. From these data, we identified a novel, dehydration-induced putative AP2/ERF transcription factor, which we predict to function as a transcriptional repressor. We also identified a dehydration-induced 'little protein' (LitP; predicted mass: 8 kDa) that is highly conserved across spermatophytes. Using qRT-PCR, we compared the expression patterns of selected genes between two related wheat genotypes that differed in their susceptibility to dehydration, and confirmed that these novel genes were highly inducible by water limitation in both genotypes, although the magnitude of induction differed.
我们使用长寡核苷酸微阵列来鉴定在耐旱六倍体面包小麦根系中,因水分胁迫而丰度增加或减少的转录本。我们观察到,脱水响应基因的主要类别(例如渗透保护剂、相容性溶质、蛋白酶、糖基转移酶/水解酶、信号转导成分、离子转运蛋白)通常与之前在其他物种和渗透胁迫中观察到的相似。更具体地说,我们着重指出了特定基因转录本表达的增加,包括那些可能与天冬酰胺、海藻糖合成、寡肽转运蛋白、金属结合蛋白、γ-氨基丁酸(GABA)分流和转录因子相关的基因。相反,我们注意到各类谷胱甘肽和硫相关酶、特定氨基酸以及多药和有毒化合物排出转运蛋白(MATE)的转录本丰度有所下降。从这些数据中,我们鉴定出一种新的、脱水诱导的假定AP2/ERF转录因子,我们预测它作为转录抑制因子发挥作用。我们还鉴定出一种脱水诱导的“小蛋白”(LitP;预测分子量:8 kDa),它在种子植物中高度保守。使用定量逆转录聚合酶链反应(qRT-PCR),我们比较了两种对脱水敏感性不同的相关小麦基因型之间选定基因的表达模式,并证实这些新基因在两种基因型中均受水分限制高度诱导,尽管诱导程度有所不同。