Weatherwax S C, Williams S A, Tingay S, Tobin E M
Department of Molecular, Cell, and Developmental Biology, University of California, Los Angeles 90095-1606, USA.
Plant Physiol. 1998 Apr;116(4):1299-305. doi: 10.1104/pp.116.4.1299.
Two important signaling systems involved in the growth and development of plants, those triggered by the photoreceptor phytochrome and the hormone abscisic acid (ABA), are involved in the regulation of expression of the NPR1 gene of Lemna gibba. We previously demonstrated that phytochrome action mediates changes in ABA levels in L. gibba, correlating with changes in gene expression evoked by stimulation of the phytochrome system. We have now further characterized phytochrome- and ABA-mediated regulation of L. gibba NPR1 gene expression using a transient particle bombardment assay, demonstrating that regulatory elements controlling responses to both stimuli reside within 156 nucleotides upstream of the transcription start. Linker scan (LS) analysis of the region from -156 to -70 was used to identify two specific requisite and nonredundant cis-acting promoter elements between -143 to -135 (LS2) and -113 to -101 (LS5). Mutation of either of these elements resulted in a coordinate loss of regulation by phytochrome and ABA. This suggests that, unlike the L. gibba Lhcb2*1 promoter, in which phytochrome and ABA regulatory elements are separable, the phytochrome response of the L. gibba NPR1 gene can be attributed to alterations in ABA levels.
植物生长和发育过程中涉及的两个重要信号系统,即由光受体光敏色素和激素脱落酸(ABA)触发的信号系统,参与了浮萍(Lemna gibba)NPR1基因表达的调控。我们之前证明,光敏色素作用介导了浮萍中ABA水平的变化,这与光敏色素系统刺激引起的基因表达变化相关。我们现在使用瞬时粒子轰击试验进一步表征了光敏色素和ABA介导的浮萍NPR1基因表达调控,证明控制对两种刺激反应的调控元件位于转录起始上游156个核苷酸内。对-156至-70区域进行接头扫描(LS)分析,以鉴定-143至-135(LS2)和-113至-101(LS5)之间的两个特定的必需且非冗余的顺式作用启动子元件。这两个元件中任何一个发生突变都会导致光敏色素和ABA协同失去调控作用。这表明,与浮萍Lhcb2*1启动子不同,其中光敏色素和ABA调控元件是可分离的,浮萍NPR1基因的光敏色素反应可归因于ABA水平的改变。