Wang Hong Wei, Kwon Hyuk Jin, Yim Won Cheol, Lim Sung Don, Moon Jun-Cheol, Lee Byung-Moo, Seo Yong Weon, Kim Wook, Jang Cheol Seong
Division of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul 136-713, Korea.
Genetica. 2010 Aug;138(8):843-52. doi: 10.1007/s10709-010-9467-7. Epub 2010 Jun 9.
Previously, the wheat non-specific lipid transfer proteins (TaLTP), members of a small multigene family, were reported to evidence a complex pattern of expression regulation. In order to assess further the expression diversity of the TaLTP genes, we have attempted to evaluate their expression profiles in responses to abiotic stresses, using semi-quantitative RT-PCR. The expression profiles generated herein revealed that the TaLTP genes in group A evidenced highly similar responses against abiotic stresses, whereas differential expression patterns among genes in each group were also observed. A total of seven promoters were fused to a GUS reporter gene and the recombinants were introduced into Arabidopsis, while three promoters evidenced non-detectible GUS activity. The promoters of TaLTP1, TaLTP7, and TaLTP10 included in group A drove strong expressions during plant development with overlapping patterns, in large part, but also exhibited distinct expression pattern, thereby suggesting subfunctionalization processing over evolutionary time. However, only trace expression in cotyledons, young emerged leaves, and epidermal cell layers of flower ovaries was driven by the promoter of TaLTP3 of group B. These results indicate that their distinct physiological functions appear to be accomplished by a subfunctionalization process involving degenerative mutations in regulatory regions.
此前有报道称,小麦非特异性脂质转移蛋白(TaLTP)是一个小多基因家族的成员,其表达调控模式复杂。为了进一步评估TaLTP基因的表达多样性,我们尝试使用半定量RT-PCR来评估它们在非生物胁迫响应中的表达谱。本文生成的表达谱显示,A组中的TaLTP基因对非生物胁迫表现出高度相似的反应,但每组基因之间也观察到了差异表达模式。总共七个启动子与GUS报告基因融合,并将重组体导入拟南芥,其中三个启动子未检测到GUS活性。A组中的TaLTP1、TaLTP7和TaLTP10的启动子在植物发育过程中驱动强表达,大部分具有重叠模式,但也表现出不同的表达模式,从而表明在进化过程中发生了亚功能化过程。然而,B组的TaLTP3启动子仅在子叶、刚长出的幼叶和花子房的表皮细胞层中驱动微量表达。这些结果表明,它们独特的生理功能似乎是通过一个涉及调控区域退化突变的亚功能化过程来实现的。