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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 |
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Language: | English |
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container_end_page | 525 |
container_issue | 3 |
container_start_page | 515 |
container_title | The Plant journal : for cell and molecular biology |
container_volume | 75 |
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 |
format | article |
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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.</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1111/tpj.12218</identifier><language>eng</language><ispartof>The Plant journal : for cell and molecular biology, 2013-08, Vol.75 (3), p.515-525</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c748-bb0af3311916b757a982b8049dfb003884c11ac399734690f14a4115436024b83</citedby><cites>FETCH-LOGICAL-c748-bb0af3311916b757a982b8049dfb003884c11ac399734690f14a4115436024b83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Guérinier, Thomas</creatorcontrib><creatorcontrib>Millan, Laurine</creatorcontrib><creatorcontrib>Crozet, Pierre</creatorcontrib><creatorcontrib>Oury, Céline</creatorcontrib><creatorcontrib>Rey, François</creatorcontrib><creatorcontrib>Valot, Benoit</creatorcontrib><creatorcontrib>Mathieu, Chantal</creatorcontrib><creatorcontrib>Vidal, Jean</creatorcontrib><creatorcontrib>Hodges, Michael</creatorcontrib><creatorcontrib>Thomas, Martine</creatorcontrib><creatorcontrib>Glab, Nathalie</creatorcontrib><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</title><title>The Plant journal : for cell and molecular biology</title><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.</description><issn>0960-7412</issn><issn>1365-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNotkLFOwzAURS0EEqUw8AdvZQj4xW7sjKiiULWCCjqwRU5qt2ldO7KzZOsPICHxh_0S2sJd7nTPlQ4ht0jv8ZCHtlnfY5qiPCM9ZNkgYcg-z0mP5hlNBMf0klzFuKYUBct4j3zNVj42Kx86q9raO_AGmlTAZDwDhJXfeuuXESbvM8hAuQUIKDv4eB0B7nffQR9WegFN8K2uHWxqp6Le734QbO02ERqrXAva6bDsjjTtY6tiHU-oSlt7nNra6HB6vyYXRtmob_67T-ajp_nwJZm-PY-Hj9OkElwmZUmVYQwxx6wUA6FymZaS8nxhSkqZlLxCVBXLc8F4llODXHHEAWcZTXkpWZ_c_WGr4GMM2hRNqLcqdAXS4qixOGgsThrZL40XZnw</recordid><startdate>201308</startdate><enddate>201308</enddate><creator>Guérinier, Thomas</creator><creator>Millan, Laurine</creator><creator>Crozet, Pierre</creator><creator>Oury, Céline</creator><creator>Rey, François</creator><creator>Valot, Benoit</creator><creator>Mathieu, Chantal</creator><creator>Vidal, Jean</creator><creator>Hodges, Michael</creator><creator>Thomas, Martine</creator><creator>Glab, Nathalie</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201308</creationdate><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</title><author>Guérinier, Thomas ; Millan, Laurine ; Crozet, Pierre ; Oury, Céline ; Rey, François ; Valot, Benoit ; Mathieu, Chantal ; Vidal, Jean ; Hodges, Michael ; Thomas, Martine ; Glab, Nathalie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c748-bb0af3311916b757a982b8049dfb003884c11ac399734690f14a4115436024b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guérinier, Thomas</creatorcontrib><creatorcontrib>Millan, Laurine</creatorcontrib><creatorcontrib>Crozet, Pierre</creatorcontrib><creatorcontrib>Oury, Céline</creatorcontrib><creatorcontrib>Rey, François</creatorcontrib><creatorcontrib>Valot, Benoit</creatorcontrib><creatorcontrib>Mathieu, Chantal</creatorcontrib><creatorcontrib>Vidal, Jean</creatorcontrib><creatorcontrib>Hodges, Michael</creatorcontrib><creatorcontrib>Thomas, Martine</creatorcontrib><creatorcontrib>Glab, Nathalie</creatorcontrib><collection>CrossRef</collection><jtitle>The Plant journal : for cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guérinier, Thomas</au><au>Millan, Laurine</au><au>Crozet, Pierre</au><au>Oury, Céline</au><au>Rey, François</au><au>Valot, Benoit</au><au>Mathieu, Chantal</au><au>Vidal, Jean</au><au>Hodges, Michael</au><au>Thomas, Martine</au><au>Glab, Nathalie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phosphorylation of p27 KIP 1 homologs KRP 6 and 7 by SNF 1‐related protein kinase–1 links plant energy homeostasis and cell proliferation</atitle><jtitle>The Plant journal : for cell and molecular biology</jtitle><date>2013-08</date><risdate>2013</risdate><volume>75</volume><issue>3</issue><spage>515</spage><epage>525</epage><pages>515-525</pages><issn>0960-7412</issn><eissn>1365-313X</eissn><abstract>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.</abstract><doi>10.1111/tpj.12218</doi><tpages>11</tpages></addata></record> |
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issn | 0960-7412 1365-313X |
language | eng |
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source | Wiley; EZB Electronic Journals Library |
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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