Two cytosolic glutamine synthetase isoforms of maize are specifically involved in the control of grain production

被引:395
作者
Martin, Antoine
Lee, Judy
Kichey, Thomas
Gerentes, Denise
Zivy, Michel
Tatout, Christophe
Dubois, Frederic
Balliau, Thierry
Valot, Benoit
Davanture, Marlene
Terce-Laforgue, Therese
Quillere, Isabelle
Coque, Marie
Gallais, Andre
Gonzalez-Moro, Maria-Begona
Bethencourt, Linda
Habash, Dimah Z.
Lea, Peter J.
Charcosset, Alain
Perez, Pascual
Murigneux, Alain
Sakakibara, Hitoshi
Edwards, Keith J.
Hirel, Bertrand [1 ]
机构
[1] INRA, Unite Nutr Azotee Plantes UR511, F-78026 Versailles, France
[2] Univ Bristol, Sch Biol Sci, Bristol BS8 1UG, Avon, England
[3] Univ Picardie, Lab Androgenese & Biotechnol, F-80039 Amiens, France
[4] Biogemma, F-63170 Clermont Ferrand, France
[5] Univ Paris Sud, INRA, CNRS, Unite Mixte Rech Genet Vegetale,Inst Natl Agron L, F-91190 Gif Sur Yvette, France
[6] Univ Basque Country, Dept Biol Vegetal & Ecol, E-48080 Bilbao, Spain
[7] Rothamsted Res, Crop Performance & Improvement Div, Harpenden AL5 2JQ, Herts, England
[8] Univ Lancaster, Dept Biol Sci, Lancaster LA1 4YQ, England
[9] Biodynam Res Team, Riken Plant Sci Ctr, Yokohama, Kanagawa 2300045, Japan
关键词
D O I
10.1105/tpc.106.042689
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The roles of two cytosolic maize glutamine synthetase isoenzymes (GS1), products of the Gln1-3 and Gln1-4 genes, were investigated by examining the impact of knockout mutations on kernel yield. In the gln1-3 and gln1-4 single mutants and the gln1-3 gln1-4 double mutant, GS mRNA expression was impaired, resulting in reduced GS1 protein and activity. The gln1-4 phenotype displayed reduced kernel size and gln1-3 reduced kernel number, with both phenotypes displayed in gln1-3 gln1-4. However, at maturity, shoot biomass production was not modified in either the single mutants or double mutants, suggesting a specific impact on grain production in both mutants. Asn increased in the leaves of the mutants during grain filling, indicating that it probably accumulates to circumvent ammonium buildup resulting from lower GS1 activity. Phloem sap analysis revealed that unlike Gln, Asn is not efficiently transported to developing kernels, apparently causing reduced kernel production. When Gln1-3 was overexpressed constitutively in leaves, kernel number increased by 30%, providing further evidence that GS1-3 plays a major role in kernel yield. Cytoimmunochemistry and in situ hybridization revealed that GS1-3 is present in mesophyll cells, whereas GS1-4 is specifically localized in the bundle sheath cells. The two GS1 isoenzymes play nonredundant roles with respect to their tissue-specific localization.
引用
收藏
页码:3252 / 3274
页数:23
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