Niu X, Narasimhan M L, Salzman R A, Bressan R A, Hasegawa P M
Center for Plant Environmental Stress Physiology, Purdue University, West Lafayette, Indiana 47907-1165.
Plant Physiol. 1993 Nov;103(3):713-8. doi: 10.1104/pp.103.3.713.
NaCl regulation of plasma membrane H(+)-ATPase gene expression in the glycophyte tobacco (Nicotiana tabacum L. var Wisconsin 38) and the halophyte Atriplex nummularia L. was evaluated by comparison of organ-specific mRNA abundance using homologous cDNA probes encoding the ATPases of the respective plants. Accumulation of mRNA was induced by NaCl in fully expanded leaves and in roots but not in expanding leaves or stems. The NaCl responsiveness of the halophyte to accumulate plasma membrane H(+)-ATPase mRNA in roots was substantially greater than that of the glycophyte. Salt-induced transcript accumulation in A. nummularia roots was localized by in situ hybridization predominantly to the elongation zone, but mRNA levels also increased in the zone of differentiation. Increased message accumulation in A. nummularia roots could be detected within 8 h after NaCl (400 mM) treatment, and maximal levels were severalfold greater than in roots of untreated control plants. NaCl-induced plasma membrane H(+)-ATPase gene expression in expanded leaves and roots presumably indicates that these organs require increased H(+)-electrochemical potential gradients for the maintenance of plant ion homeostasis for salt adaptation. The greater capacity of the halophyte to induce plasma membrane H(+)-ATPase gene expression in response to NaCl may be a salt-tolerance determinant.
通过使用编码各植物ATP酶的同源cDNA探针比较器官特异性mRNA丰度,评估了NaCl对甜土植物烟草(Nicotiana tabacum L. var Wisconsin 38)和盐生植物滨藜(Atriplex nummularia L.)质膜H(+)-ATP酶基因表达的调控。NaCl诱导完全展开的叶片和根中mRNA积累,但在正在展开的叶片或茎中未诱导。盐生植物根中积累质膜H(+)-ATP酶mRNA对NaCl的反应性显著大于甜土植物。滨藜根中盐诱导的转录本积累通过原位杂交主要定位于伸长区,但在分化区mRNA水平也增加。在NaCl(400 mM)处理后8小时内可检测到滨藜根中mRNA积累增加,最大水平比未处理对照植物的根高几倍。NaCl诱导展开叶片和根中质膜H(+)-ATP酶基因表达,推测这些器官需要增加H(+)-电化学势梯度以维持植物离子稳态以适应盐分。盐生植物对NaCl反应诱导质膜H(+)-ATP酶基因表达的能力更强可能是耐盐性的一个决定因素。