The GSK3/Shaggy family of serine/threonine protein kinases is involved in a series of biological processes in animals, plants and yeast [Charrier et al. (2002) Plant Physiol 130:577–590; Jope and Johnson (2004) Trends Biochem Sci 29:95–102; Li and Nam (2002) Science 295:1299–1301; Piao et al. (2001) Plant J 27:305–314]. In Arabidopsis thaliana, out of the 10 members of the GSK3/Shaggy-like gene family (AtSKs), a biological function has been assigned to only 1 member (AtSK2-1) by mutation. In the present work, a study was undertaken to elucidate the function of AtSK3-2. We have generated mutated versions of the A. thaliana Shaggy-like kinase 3-2 (AtSK3-2), in which Lys167 and Arg178, respectively homologus to Lys85 and Arg96 of the mammal GSK3β, were modified into Ala by site-directed mutagenesis. In vitro kinase activity assays of the mutated recombinant protein AtSK3-2-R178A showed that the “primed activity” of the mutated kinase was reduced by 90% while the “non-primed” activity was only 20% reduced compared to the wild-type protein kinase. However, the mutant protein AtSK3-2-K167A showed no activity. Arabidopsis transgenic lines over-expressing AtSK3-2-R178A displayed smaller floral organs, namely pedicels, sepals and petals. Conversely, over-expression of both the wild-type AtSK3-2 protein and the AtSK3-2-K167A mutated version, displayed no altered morphogenesis. Scanning electron microscopic analyses of the AtSK3-2-R178A transgenic plants clearly showed a reduced cell size in flower organs, in which quantitative RT-PCR expression analyses of cell wall expansion enzymes showed reduced transcript levels of three xyloglucan endotransglycosylases (XET), namely XTH22 (TCH4), XTH23 (XTR6) and XTH30 (XTR4). Our data show that AtSK3-2 plays an important role in the control of cell elongation in flower development.
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Carnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USACarnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA
Hsu, Chuan-Chih
Park, Chan Ho
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Carnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USACarnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA
Park, Chan Ho
Kim, Tae-Wuk
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Carnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA
Hanyang Univ, Dept Life Sci, Seoul 04763, South Korea
Hanyang Univ, Res Inst Nat Sci, Seoul 04763, South KoreaCarnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA
Kim, Tae-Wuk
Zhu, Jia-Ying
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Carnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USACarnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA
Zhu, Jia-Ying
Hsiao, Yu-Chun
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Carnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USACarnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA
Hsiao, Yu-Chun
Branon, Tess
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Stanford Univ, Dept Genet Biol, Stanford, CA 94305 USA
Stanford Univ, Dept Chem, Stanford, CA 94305 USA
Chan Zuckerberg Biohub, San Francisco, CA USACarnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA
Branon, Tess
Ting, Alice Y.
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Stanford Univ, Dept Genet Biol, Stanford, CA 94305 USA
Stanford Univ, Dept Chem, Stanford, CA 94305 USA
Chan Zuckerberg Biohub, San Francisco, CA USACarnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA
Ting, Alice Y.
Xu, Shou-Ling
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Carnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USACarnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA
Xu, Shou-Ling
Wang, Zhi-Yong
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Carnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USACarnegie Inst Sci, Dept Plant Biol, Stanford, CA 94305 USA