TY - JOUR
T1 - Cell type distinct accumulations of mRNA and protein for NADH-dependent glutamate synthase in rice roots in response to the supply of NH4+
AU - Ishiyama, Keiki
AU - Kojima, Soichi
AU - Takahashi, Hideki
AU - Hayakawa, Toshihiko
AU - Yamaya, Tomoyuki
N1 - Funding Information:
We thank Dr. Taku Demura for supporting in situ hybridization technique at Plant Science Center, RIKEN (Yokohama, Japan). This work was supported in part by a program of CREST of JST (Japan Science Technology) and in part by Grant-in-Aid from the Ministry of Education, Science, Culture, Technology, and Sport of Japan (Nos. 12460029, 14360035 and 14654160).
PY - 2003/6/1
Y1 - 2003/6/1
N2 - Transient and NH4+-inducible accumulation of the mRNA for NADH-dependent glutamate synthase (NADH-GOGAT; EC 1.4.1.14) in the roots of rice seedlings was analyzed in situ to identify the cell types responsible for the induction. The mRNA was detected specifically in sclerenchyma cells (the third cell-layer from the root surface), and the maximal accumulation was seen at 3-6 h following the supply of NH4+ ions. Expression of the NADH-GOGAT gene in sclerenchyma cells was also confirmed using transgenic rice plants expressing GUS reporter gene under the control of rice NADH-GOGAT promoter. On the other hand, clear signals for the NADH-GOGAT protein were detected in epidermial cells and exodermal cells (the first and second cell layers from the root surface) at 12 h, following the supply of NH4+ ions. The distinct localization of mRNA and protein for NADH-GOGAT suggests that either the mRNA or the translated protein in the sclerenchyma cells is migrated to the root surface. In contrast to NADH-GOGAT protein, Fd-GOGAT (EC 1.4.7.1) protein was detected in sclerenchyma cells, cortex cells, and stele in the rice roots. The distinct localization of the two GOGAT species indicates that they have different roles in the nitrogen metabolism in rice roots.
AB - Transient and NH4+-inducible accumulation of the mRNA for NADH-dependent glutamate synthase (NADH-GOGAT; EC 1.4.1.14) in the roots of rice seedlings was analyzed in situ to identify the cell types responsible for the induction. The mRNA was detected specifically in sclerenchyma cells (the third cell-layer from the root surface), and the maximal accumulation was seen at 3-6 h following the supply of NH4+ ions. Expression of the NADH-GOGAT gene in sclerenchyma cells was also confirmed using transgenic rice plants expressing GUS reporter gene under the control of rice NADH-GOGAT promoter. On the other hand, clear signals for the NADH-GOGAT protein were detected in epidermial cells and exodermal cells (the first and second cell layers from the root surface) at 12 h, following the supply of NH4+ ions. The distinct localization of mRNA and protein for NADH-GOGAT suggests that either the mRNA or the translated protein in the sclerenchyma cells is migrated to the root surface. In contrast to NADH-GOGAT protein, Fd-GOGAT (EC 1.4.7.1) protein was detected in sclerenchyma cells, cortex cells, and stele in the rice roots. The distinct localization of the two GOGAT species indicates that they have different roles in the nitrogen metabolism in rice roots.
KW - Cellular localization
KW - NADH-dependent glutamate synthase (EC 1.4.1.14)
KW - NH supply
KW - Rice root
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U2 - 10.1016/S0981-9428(03)00078-0
DO - 10.1016/S0981-9428(03)00078-0
M3 - Article
AN - SCOPUS:0242416925
SN - 0981-9428
VL - 41
SP - 643
EP - 647
JO - Plant Physiology and Biochemistry
JF - Plant Physiology and Biochemistry
IS - 6-7
ER -