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Phosphorylation of p27 KIP 1 homologs KRP 6 and 7 by SNF 1‐related protein kinase–1 links plant energy homeostasis and cell proliferation

SNF 1‐related protein kinase–1 (Sn RK 1), the plant kinase homolog of mammalian AMP ‐activated protein kinase ( AMPK ), is a sensor that maintains cellular energy homeostasis via control of anabolism/catabolism balance. AMPK ‐dependent phosphorylation of p27 KIP 1 affects cell‐cycle progression, aut...

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Published in:The Plant journal : for cell and molecular biology 2013-08, Vol.75 (3), p.515-525
Main Authors: Guérinier, Thomas, Millan, Laurine, Crozet, Pierre, Oury, Céline, Rey, François, Valot, Benoit, Mathieu, Chantal, Vidal, Jean, Hodges, Michael, Thomas, Martine, Glab, Nathalie
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container_title The Plant journal : for cell and molecular biology
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creator Guérinier, Thomas
Millan, Laurine
Crozet, Pierre
Oury, Céline
Rey, François
Valot, Benoit
Mathieu, Chantal
Vidal, Jean
Hodges, Michael
Thomas, Martine
Glab, Nathalie
description SNF 1‐related protein kinase–1 (Sn RK 1), the plant kinase homolog of mammalian AMP ‐activated protein kinase ( AMPK ), is a sensor that maintains cellular energy homeostasis via control of anabolism/catabolism balance. AMPK ‐dependent phosphorylation of p27 KIP 1 affects cell‐cycle progression, autophagy and apoptosis. Here, we show that Sn RK 1 phosphorylates the Arabidopsis thaliana cyclin‐dependent kinase inhibitor p27 KIP 1 homologs At KRP 6 and At KRP 7, thus extending the role of this kinase to regulation of cell‐cycle progression. At KRP 6 and 7 were phosphorylated in vitro by a recombinant activated catalytic subunit of Sn RK 1 (AtSn RK 1α1). Tandem mass spectrometry and site‐specific mutagenesis identified Thr152 and Thr151 as the phosphorylated residues on At KRP 6‐ and At KRP 7, respectively. AtSn RK 1 physically interacts with At KRP 6 in the nucleus of transformed BY –2 tobacco protoplasts, but, in contrast to mammals, the At KRP 6 Thr152 phosphorylation state alone did not modify its nuclear localization. Using a heterologous yeast system, consisting of a cdc28 yeast mutant complemented by A. thaliana CDKA ;1, cell proliferation was shown to be abolished by At KRP 6 WT and by the non‐phosphorylatable form At KRP 6 T152A , but not by the phosphorylation‐mimetic form At KRP 6 T152D . Moreover, A. thaliana Sn RK 1α1/ KRP 6 double over‐expressor plants showed an attenuated At KRP 6‐associated phenotype (strongly serrated leaves and inability to undergo callogenesis). Furthermore, this severe phenotype was not observed in At KRP 6 T152D over‐expressor plants. Overall, these results establish that the energy sensor AtSn RK 1 plays a cardinal role in the control of cell proliferation in A. thaliana plants through inhibition of At KRP 6 biological function by phosphorylation.
doi_str_mv 10.1111/tpj.12218
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Using a heterologous yeast system, consisting of a cdc28 yeast mutant complemented by A. thaliana CDKA ;1, cell proliferation was shown to be abolished by At KRP 6 WT and by the non‐phosphorylatable form At KRP 6 T152A , but not by the phosphorylation‐mimetic form At KRP 6 T152D . Moreover, A. thaliana Sn RK 1α1/ KRP 6 double over‐expressor plants showed an attenuated At KRP 6‐associated phenotype (strongly serrated leaves and inability to undergo callogenesis). Furthermore, this severe phenotype was not observed in At KRP 6 T152D over‐expressor plants. 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title Phosphorylation of p27 KIP 1 homologs KRP 6 and 7 by SNF 1‐related protein kinase–1 links plant energy homeostasis and cell proliferation
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