Shi L, Twary S N, Yoshioka H, Gregerson R G, Miller S S, Samac D A, Gantt J S, Unkefer P J, Vance C P
U.S. Department of Agnculture, Agricultural Research Service, University of Minnesota, St. Paul 55108, USA.
Plant Cell. 1997 Aug;9(8):1339-56. doi: 10.1105/tpc.9.8.1339.
Asparagine, the primary assimilation product from N2 fixation in temperate legumes and the predominant nitrogen transport product in many plant species, is synthesized via asparagine synthetase (AS; EC 6.3.5.4). Here, we report the isolation and characterization of a cDNA and a gene encoding the nodule-enhanced form of AS from alfalfa. The AS gene is comprised of 13 exons separated by 12 introns. The 5' flanking region of the AS gene confers nodule-enhanced reporter gene activity in transformed alfalfa. This region also confers enhanced reporter gene activity in dark-treated leaves. These results indicate that the 5' upstream region of the AS gene contains elements that affect expression in root nodules and leaves. Both AS mRNA and enzyme activity increased approximately 10- to 20-fold during the development of effective nodules. Ineffective nodules have strikingly reduced amounts of AS transcript. Alfalfa leaves have quite low levels of AS mRNA and protein; however, exposure to darkness resulted in a considerable increase in both. In situ hybridization with effective nodules and beta-glucuronidase staining of nodules from transgenic plants showed that AS is expressed in both infected and uninfected cells of the nodule symbiotic zone and in the nodule parenchyma. RNA gel blot analysis and in situ hybridization results are consistent with the hypothesis that initial AS expression in nodules is independent of nitrogenase activity.
天冬酰胺是温带豆科植物中固氮作用产生的主要同化产物,也是许多植物物种中主要的氮转运产物,它通过天冬酰胺合成酶(AS;EC 6.3.5.4)合成。在此,我们报道了从苜蓿中分离和鉴定一个编码结节增强型AS的cDNA和基因。AS基因由13个外显子组成,被12个内含子隔开。AS基因的5'侧翼区域在转化的苜蓿中赋予结节增强型报告基因活性。该区域在黑暗处理的叶片中也赋予增强的报告基因活性。这些结果表明,AS基因的5'上游区域含有影响根瘤和叶片中表达的元件。在有效根瘤发育过程中,AS mRNA和酶活性均增加了约10至20倍。无效根瘤中AS转录本的量显著减少。苜蓿叶片中AS mRNA和蛋白质水平相当低;然而,暴露于黑暗中会导致两者都大幅增加。对有效根瘤进行原位杂交以及对转基因植物根瘤进行β-葡萄糖醛酸酶染色表明,AS在根瘤共生区的感染细胞和未感染细胞以及根瘤薄壁组织中均有表达。RNA凝胶印迹分析和原位杂交结果与根瘤中AS的初始表达独立于固氮酶活性这一假设一致。