Reverse genetics approach to characterize a function of NADH-glutamate synthase1 in rice plants

被引:74
|
作者
Tamura, Wataru [1 ]
Hidaka, Yusuke [1 ]
Tabuchi, Mayumi [1 ]
Kojima, Soichi [1 ]
Hayakawa, Toshihiko [1 ]
Sato, Tadashi [2 ]
Obara, Mitsuhiro [3 ]
Kojima, Mikiko [4 ]
Sakakibara, Hitoshi [4 ]
Yamaya, Tomoyuki [1 ]
机构
[1] Tohoku Univ, Grad Sch Agr Sci, Aoba Ku, Sendai, Miyagi 9818555, Japan
[2] Tohoku Univ, Grad Sch Life Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
[3] Iwate Biotechnol Res Ctr, Kitakami, Iwate 0240003, Japan
[4] RIKEN Plant Sci Ctr, Yokohama, Kanagawa 2300045, Japan
关键词
Ammonium assimilation; Glutamate synthase; Glutamine synthetase; Oryza sativa L; Retrotransposon; Rice; CELLULAR-LOCALIZATION; AMMONIUM ASSIMILATION; NITROGEN-METABOLISM; VASCULAR BUNDLES; LEAF BLADES; ROOT-GROWTH; SYNTHETASE; PROTEIN; EXPRESSION; MAIZE;
D O I
10.1007/s00726-010-0531-5
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
Rice plants grown in anaerobic paddy soil prefer to use ammonium ion as an inorganic nitrogen source for their growth. The ammonium ions are assimilated by the coupled reaction of glutamine synthetase (GS) and glutamate synthase (GOGAT). In rice, there is a small gene family for GOGAT: there are two NADH-dependent types and one ferredoxin (Fd)-dependent type. Fd-GOGAT is important in the re-assimilation of photorespiratorily generated ammonium ions in chloroplasts. Although cell-type and age-dependent expression of two NADH-GOGAT genes has been well characterized, metabolic function of individual gene product is not fully understood. Reverse genetics approach is a direct way to characterize functions of isoenzymes. We have isolated a knockout rice mutant lacking NADH-dependent glutamate synthase1 (NADH-GOGAT1) and our studies show that this isoenzyme is important for primary ammonium assimilation in roots at the seedling stage. NADH-GOGAT1 is also important in the development of active tiller number, when the mutant was grown in paddy field until the harvest. Expression of NADH-GOGAT2 and Fd-GOGAT in the mutant was identical with that in wild-type, suggesting that these GOGATs are not able to compensate for NADH-GOGAT1 function.
引用
收藏
页码:1003 / 1012
页数:10
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