cDNA microarray analysis of gene expression during Fe-deficiency stress in barley suggests that polar transport of vesicles is implicated in phytosiderophore secretion in Fe-deficient barley roots

被引:131
作者
Negishi, T
Nakanishi, H
Yazaki, J
Kishimoto, N
Fujii, F
Shimbo, K
Yamamoto, K
Sakata, K
Sasaki, T
Kikuchi, S
Mori, S
Nishizawa, NK
机构
[1] Univ Tokyo, Lab Plant Biotechnol, Bunkyo Ku, Tokyo 1138657, Japan
[2] Univ Tokyo, Lab Plant Mol Physiol, Bunkyo Ku, Tokyo 1138657, Japan
[3] Inst Soc Technoinnovat Agr Forestry & Fisheries, Tsukuba, Ibaraki 3050854, Japan
[4] Natl Inst Agrobiol Sci, Tsukuba, Ibaraki 3058602, Japan
[5] Japan Sci & Technol Corp, Core Res Evolut Sci & Technol, Tokyo, Japan
关键词
cDNA microarray; diurnal rhythm; Fe-deficiency; methionine synthesis; mugineic acid family phytosiderophores; vesicle transport;
D O I
10.1046/j.1365-313X.2002.01270.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
To acquire Fe from soil, graminaceous plants secrete mugineic acid family phytosiderophores (MAs) from their roots. The secretion of MAs increases in response to Fe deficiency, and shows a distinct diurnal rhythm. We used a microarray that included 8987 cDNAs of rice EST clones to examine gene expression profiles in barley roots during Fe-deficiency stress. Approximately 200 clones were identified as Fe-deficiency-inducible genes, of which seven had been identified previously. In order to meet the increased demand for methionine to produce MAs, Fe-deficiency enhances the expression of genes that participate in methionine synthesis, as well as recycling methionine through the Yang cycle. Of these 200 genes, approximately 50 exhibited different transcription levels in Fe-deficient roots at noon and at night. Northern blot analysis of time course experiments confirmed that five of these genes exhibited a diurnal change in their level of expression. The diurnal changes in the expression of these genes suggest that polar vesicle transport is involved in the diurnal secretion of MAs.
引用
收藏
页码:83 / 94
页数:12
相关论文
共 48 条
[1]   Identification of the SAAT gene involved in strawberry flavor biogenesis by use of DNA microarrays [J].
Aharoni, A ;
Keizer, LCP ;
Bouwmeester, HJ ;
Sun, ZK ;
Alvarez-Huerta, M ;
Verhoeven, HA ;
Blaas, J ;
van Houwelingen, AMML ;
De Vos, RCH ;
van der Voet, H ;
Jansen, RC ;
Guis, M ;
Mol, J ;
Davis, RW ;
Schena, M ;
van Tunen, AJ ;
O'Connell, AP .
PLANT CELL, 2000, 12 (05) :647-661
[2]   A Rab1 GTPase is required for transport between the endoplasmic reticulum and Golgi apparatus and for normal Golgi movement in plants [J].
Batoko, H ;
Zheng, HQ ;
Hawes, C ;
Moore, I .
PLANT CELL, 2000, 12 (11) :2201-2217
[3]   Distribution of folate derivatives and enzymes for synthesis of 10-formyltetrahydrofolate in cytosolic and mitochondrial fractions of pea leaves [J].
Chen, LF ;
Chan, SY ;
Cossins, EA .
PLANT PHYSIOLOGY, 1997, 115 (01) :299-309
[4]   Maize yellow stripe1 encodes a membrane protein directly involved in Fe(III) uptake [J].
Curie, C ;
Panaviene, Z ;
Loulergue, C ;
Dellaporta, SL ;
Briat, JF ;
Walker, EL .
NATURE, 2001, 409 (6818) :346-349
[5]   New structure and function in plant K+ channels: KCO1, an outward rectifier with a steep Ca2+ dependency [J].
Czempinski, K ;
Zimmermann, S ;
Ehrhardt, T ;
MullerRober, B .
EMBO JOURNAL, 1997, 16 (10) :2565-2575
[6]   A MAIZE PROTEIN ASSOCIATED WITH THE G-BOX BINDING COMPLEX HAS HOMOLOGY TO BRAIN REGULATORY PROTEINS [J].
DEVETTEN, NC ;
LU, GH ;
FERL, RJ .
PLANT CELL, 1992, 4 (10) :1295-1307
[7]  
GANET P, 1996, BIOCHEM MOL BIOL INT, V40, P469
[8]   Cloning of nicotianamine synthase genes, novel genes involved in the biosynthesis of phytosiderophores [J].
Higuchi, K ;
Suzuki, K ;
Nakanishi, H ;
Yamaguchi, H ;
Nishizawa, NK ;
Mori, S .
PLANT PHYSIOLOGY, 1999, 119 (02) :471-479
[9]   Induced activity of adenine phosphoribosyltransferase (APRT) in iron-deficient barley roots: a possible role for phytosiderophore production [J].
Itai, R ;
Suzuki, K ;
Yamaguchi, H ;
Nakanishi, H ;
Nishizawa, NK ;
Yoshimura, E ;
Mori, S .
JOURNAL OF EXPERIMENTAL BOTANY, 2000, 51 (348) :1179-1188
[10]  
KATRIEN MD, 2000, PLANT CELL, V12, P637