Expression analysis of a high-affinity nitrate transporter isolated from Arabidopsis thaliana by differential display

被引:140
作者
Filleur, S [1 ]
Daniel-Vedele, F [1 ]
机构
[1] INRA, Biol Cellulaire Lab, F-78026 Versailles, France
关键词
Arabidopsis; gene expression (differential display); gene regulation (N-source); nitrate transporter;
D O I
10.1007/s004250050505
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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 mu M 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.
引用
收藏
页码:461 / 469
页数:9
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