A 1 kb promoter fragment of the Nii1 gene, encoding a tobacco foliar nitrit
e reductase, has been fused to the beta-glucuronidase (Gus) or luciferase (
Luc) reporter genes. These constructs were introduced in Arabidopsis thalia
na by in planta infiltration. Analysis of transformants shows that GUS or L
UC activities are induced by nitrate. Deletions of the Nii1 promoter fused
to the Luc gene have been made in order to delineate cis-sequences necessar
y for nitrate induction. The Nii1, Delta C, Delta M and Delta H constructs
ending, respectively at - 962, - 678, - 202 and - 76 bp before the putative
transcription start of the Nii1 gene were fused transcriptionally to the L
uc reporter gene. Analysis of LUC activities shows that nitrate induction o
ccurs in the Delta MLuc construct, so promoter sequences required for nitra
te induction of the reporter gene are retained in the proximal 200 bp fragm
ent of the promoter. For the smallest construct, nitrate inducibility is ma
intained in one transformant. Yet, the low level of LUC activity detected i
n the other transformants does not allow us to assume that nitrate regulato
ry elements are still present in the Delta HLuc construct. We will discuss
these results in relation to those obtained with deletions of other Nia or
Nii promoters by different laboratories. (C) 1998 Elsevier Science Ireland
Ltd. All rights reserved.