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Journal of Experimental Botany, Vol. 52, No. 359, pp. 1209-1217, June 1, 2001
© 2001 Oxford University Press


Original Papers

Mapping of QTLs associated with cytosolic glutamine synthetase and NADH-glutamate synthase in rice (Oryza sativa L.)

Mitsuhiro Obara1, Makoto Kajiura1, Yoshimichi Fukuta2, Masahiro Yano3, Makoto Hayashi1,4, Tomoyuki Yamaya1,5 and Tadashi Sato6,7

1 Department of Applied Plant Science, Graduate School of Agricultural Sciences, Tohoku University, 1-1 Tsutsumidori-Amamiyamachi, Aoba-ku, Sendai 981-8555, Japan
2 Plant Breeding, Genetics and Biochemistry Division, International Rice Research Institute, MCPO BOX 3127,1271 Makati City, Philippines
3 Department of Molecular Genetics, National Institute of Agrobiological Resources, 2-1-2 Kannondai, Tsukuba 305-8602, Japan
4 Department of Cell Biology, National Institute for Basic Biology, Okazaki 444-8585, Japan
5 Plant Science Center, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan
6 Graduate School of Life Science, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577, Japan

Ninety-eight backcross inbred lines (BC1F6) developed between Nipponbare, a japonica rice, and Kasalath, an indica rice were employed to detect putative quantitative trait loci (QTLs) associated with the contents of cytosolic glutamine synthetase (GS1; EC 6.3.1.2) and NADH-glutamate synthase (NADH-GOGAT; EC 1.4.1.14) in leaves. Immunoblotting analyses showed transgressive segregations toward lower or greater contents of these enzyme proteins in these backcross inbred lines. Seven chromosomal QTL regions for GS1 protein content and six for NADH-GOGAT protein content were detected. Some of these QTLs were located in QTL regions for various biochemical and physiological traits affected by nitrogen recycling. These findings suggested that the variation in GS1 and NADH-GOGAT protein contents in this population is related to the changes in the rate of nitrogen recycling from senescing organs to developing organs, leading to changes in these physiological traits. Furthermore, a structural gene for GS1 was mapped between two RFLP markers, C560 and C1408, on chromosome 2 and co-located in the QTL region for one-spikelet weight. A QTL region for NADH-GOGAT protein content was detected at the position mapped for the NADH-GOGAT structural gene on chromosome 1. A QTL region for soluble protein content in developing leaves was also detected in this region. Although fine mapping is required to identify individual genes in the future, QTL analysis could be a useful post-genomic tool to study the gene functions for regulation of nitrogen recycling in rice.

Key words: Cytosolic glutamine synthetase, NADH-glutamate synthase, nitrogen recycling, QTL, rice (Oryza sativa L.).


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