Filleur S, Daniel-Vedele F
Laboratoire de Biologie Cellulaire, INRA, Versailles, France.
Planta. 1999 Jan;207(3):461-9. doi: 10.1007/s004250050505.
We used the differential display technique on total RNAs from roots of Arabidopsis thaliana (L.) Heynh. plants which had or had not been induced for 2 h by nitrate. One isolated cDNA clone, designated Nrt2:1At, was found to code for a putative high-affinity nitrate transporter. Two genomic sequences homologous to Nrt2:1At were found to be localized on the same fragment of chromosome 1 in the Arabidopsis genome. Expression analyses of both low- and high-affinity nitrate transporter genes, respectively Nrt1:1At (previously named Chl1) and Nrt2:1At, were carried out on plants grown under different nitrogen regimes. In this paper, we show that both genes are induced by very low levels of nitrate (50 microM KNO3). However, stronger induction was observed with Nrt2:1At than with Nrt1:1At. Moreover, these two genes, although both over-expressed in a nitrate-reductase-deficient mutant, were differently regulated when N-sufficient wild-type or mutant plants were transferred to an N-free medium. Indeed, the steady-state amounts of Nrt1:1At mRNA declined whereas the amount of Nrt2:1At mRNA increased, probably reflecting the de-repression of the high-affinity transport system during N-starvation.
我们对经硝酸盐诱导2小时或未诱导的拟南芥植株根部的总RNA运用了差异显示技术。发现一个分离的cDNA克隆,命名为Nrt2:1At,编码一种假定的高亲和力硝酸盐转运蛋白。在拟南芥基因组中,发现与Nrt2:1At同源的两个基因组序列定位于第1号染色体的同一片段上。分别对在不同氮素供应条件下生长的植株进行了低亲和力和高亲和力硝酸盐转运蛋白基因(分别为Nrt1:1At(先前命名为Chl1)和Nrt2:1At)的表达分析。在本文中,我们表明这两个基因都受到极低水平硝酸盐(50微摩尔硝酸钾)的诱导。然而,观察到Nrt2:1At的诱导作用比Nrt1:1At更强。此外,这两个基因虽然在硝酸盐还原酶缺陷型突变体中都过表达,但当氮素充足的野生型或突变体植株转移到无氮培养基中时,它们受到的调控方式不同。实际上,Nrt1:1At mRNA的稳态量下降,而Nrt2:1At mRNA的量增加,这可能反映了氮饥饿期间高亲和力转运系统的去抑制作用。