TY - JOUR
T1 - AtIPT3 is a key determinant of nitrate-dependent cytokinin biosynthesis in Arabidopsis
AU - Takei, Kentaro
AU - Ueda, Nanae
AU - Aoki, Koh
AU - Kuromori, Takashi
AU - Hirayama, Takashi
AU - Shinozaki, Kazuo
AU - Yamaya, Tomoyuki
AU - Sakakibara, Hitoshi
N1 - Funding Information:
We thank Dr. Keiko Yonekura-Sakakibara (RIKEN) for helpful comments on the manuscript. This study was partly supported by Grants-in-Aids for Scientific Research on Priority Areas (number 12142202 to HS) and by Grants-in-Aids for Scientific Research for the Encouragement of Young Scientists (B) (number 15770035 to KT) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), Japan.
PY - 2004/8
Y1 - 2004/8
N2 - We analyzed the spatial expression pattern of Arabidopsis thaliana adenosine phosphates-isopentenyltransferase genes (AtIPT1, AtIPT3 to AtIPT8) and the effect of inorganic nitrogen sources on their regulation. In mature plants, the AtIPTs were differentially expressed in various tissues including the roots, leaves, stems, flowers and siliques. In transgenic seedlings expressing a gene for green fluorescent protein (GFP) driven by the AtIPT promoters, AtIPT1::GFP was predominantly expressed in the vascular stele of the roots, AtIPT3::GFP was in the phloem companion cells, AtIPT5::GFP was in the lateral root primordium and pericycle, and AtIPT7::GFP was in both the vascular stele and the phloem companion cells of the roots. In a long-term treatment, the accumulation level of AtIPT5 transcript was correlated with the concentrations of NO3- and NH4+ in the growth medium. However, under nitrogen-limited conditions, AtIPT3 expression was rapidly induced by NO3- in the seedlings accompanying the accumulation of cytokinins, whereas AtIPT5 expression was little affected. The NO3--dependent accumulation of both the AtIPT3 transcript and the cytokinins was markedly reduced in a Ds transposon-insertion mutant of AtIPT3. These results suggest that nitrogen availability differentially regulates expression of AtIPT3 and AtIPT5, and that AtIPT3 is a key determinant of cytokinin biosynthesis in response to rapid changes in the availability of NO3-.
AB - We analyzed the spatial expression pattern of Arabidopsis thaliana adenosine phosphates-isopentenyltransferase genes (AtIPT1, AtIPT3 to AtIPT8) and the effect of inorganic nitrogen sources on their regulation. In mature plants, the AtIPTs were differentially expressed in various tissues including the roots, leaves, stems, flowers and siliques. In transgenic seedlings expressing a gene for green fluorescent protein (GFP) driven by the AtIPT promoters, AtIPT1::GFP was predominantly expressed in the vascular stele of the roots, AtIPT3::GFP was in the phloem companion cells, AtIPT5::GFP was in the lateral root primordium and pericycle, and AtIPT7::GFP was in both the vascular stele and the phloem companion cells of the roots. In a long-term treatment, the accumulation level of AtIPT5 transcript was correlated with the concentrations of NO3- and NH4+ in the growth medium. However, under nitrogen-limited conditions, AtIPT3 expression was rapidly induced by NO3- in the seedlings accompanying the accumulation of cytokinins, whereas AtIPT5 expression was little affected. The NO3--dependent accumulation of both the AtIPT3 transcript and the cytokinins was markedly reduced in a Ds transposon-insertion mutant of AtIPT3. These results suggest that nitrogen availability differentially regulates expression of AtIPT3 and AtIPT5, and that AtIPT3 is a key determinant of cytokinin biosynthesis in response to rapid changes in the availability of NO3-.
KW - Ammonium ions
KW - Arabidopsis
KW - Cytokinin
KW - Isopentenyltransferase
KW - Nitrate ions
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U2 - 10.1093/pcp/pch119
DO - 10.1093/pcp/pch119
M3 - Article
C2 - 15356331
AN - SCOPUS:4644362844
SN - 0032-0781
VL - 45
SP - 1053
EP - 1062
JO - Plant and Cell Physiology
JF - Plant and Cell Physiology
IS - 8
ER -