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A Rice gid1 Suppressor Mutant Reveals That Gibberellin Is Not Always Required for Interaction between Its Receptor, GID1, and DELLA Proteins

Yuko Yamamoto, Takaaki Hirai, Eiji Yamamoto, Mayuko Kawamura, Tomomi Sato, Hidemi Kitano, Makoto Matsuoka, Miyako Ueguchi-Tanaka
Yuko Yamamoto
aBioscience and Biotechnology Center, Nagoya University, Nagoya 464-8601, Japan
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Takaaki Hirai
aBioscience and Biotechnology Center, Nagoya University, Nagoya 464-8601, Japan
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Eiji Yamamoto
aBioscience and Biotechnology Center, Nagoya University, Nagoya 464-8601, Japan
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Mayuko Kawamura
aBioscience and Biotechnology Center, Nagoya University, Nagoya 464-8601, Japan
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Tomomi Sato
bDepartment of Structural Biology, Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan
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Hidemi Kitano
aBioscience and Biotechnology Center, Nagoya University, Nagoya 464-8601, Japan
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Makoto Matsuoka
aBioscience and Biotechnology Center, Nagoya University, Nagoya 464-8601, Japan
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Miyako Ueguchi-Tanaka
aBioscience and Biotechnology Center, Nagoya University, Nagoya 464-8601, Japan
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  • For correspondence: mueguchi@nuagr1.agr.nagoya-u.ac.jp

Published November 2010. DOI: https://doi.org/10.1105/tpc.110.074542

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  • © 2010 American Society of Plant Biologists

Abstract

To investigate gibberellin (GA) signaling using the rice (Oryza sativa) GA receptor GIBBERELLIN-INSENSITIVE DWARF1 (GID1) mutant gid1-8, we isolated a suppressor mutant, Suppressor of gid1-1 (Sgd-1). Sgd-1 is an intragenic mutant containing the original gid1-8 mutation (L45F) and an additional amino acid substitution (P99S) in the loop region. GID1P99S interacts with the rice DELLA protein SLENDER RICE1 (SLR1), even in the absence of GA. Substitution of the 99th Pro with other amino acids revealed that substitution with Ala (P99A) caused the highest level of GA-independent interaction. Physicochemical analysis using surface plasmon resonance revealed that GID1P99A has smaller Ka (association) and Kd (dissociation) values for GA4 than does wild-type GID1. This suggests that the GID1P99A lid is at least partially closed, resulting in both GA-independent and GA-hypersensitive interactions with SLR1. One of the three Arabidopsis thaliana GID1s, At GID1b, can also interact with DELLA proteins in the absence of GA, so we investigated whether GA-independent interaction of At GID1b depends on a mechanism similar to that of rice GID1P99A. Substitution of the loop region or a few amino acids of At GID1b with those of At GID1a diminished its GA-independent interaction with GAI while maintaining the GA-dependent interaction. Soybean (Glycine max) and Brassica napus also have GID1s similar to At GID1b, indicating that these unique GID1s occur in various dicots and may have important functions in these plants.

  • Received February 5, 2010.
  • Revised September 21, 2010.
  • Accepted November 1, 2010.
  • Published November 23, 2010.

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A Rice gid1 Suppressor Mutant Reveals That Gibberellin Is Not Always Required for Interaction between Its Receptor, GID1, and DELLA Proteins
Yuko Yamamoto, Takaaki Hirai, Eiji Yamamoto, Mayuko Kawamura, Tomomi Sato, Hidemi Kitano, Makoto Matsuoka, Miyako Ueguchi-Tanaka
The Plant Cell Nov 2010, 22 (11) 3589-3602; DOI: 10.1105/tpc.110.074542

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A Rice gid1 Suppressor Mutant Reveals That Gibberellin Is Not Always Required for Interaction between Its Receptor, GID1, and DELLA Proteins
Yuko Yamamoto, Takaaki Hirai, Eiji Yamamoto, Mayuko Kawamura, Tomomi Sato, Hidemi Kitano, Makoto Matsuoka, Miyako Ueguchi-Tanaka
The Plant Cell Nov 2010, 22 (11) 3589-3602; DOI: 10.1105/tpc.110.074542
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The Plant Cell Online: 22 (11)
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Vol. 22, Issue 11
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