-
Je něco špatně v tomto záznamu ?
The Cytokinin Oxidase/Dehydrogenase CKX1 Is a Membrane-Bound Protein Requiring Homooligomerization in the Endoplasmic Reticulum for Its Cellular Activity
MCE. Niemann, H. Weber, T. Hluska, G. Leonte, SM. Anderson, O. Novák, A. Senes, T. Werner,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
NLK
Free Medical Journals
od 1926 do Před 1 rokem
Open Access Digital Library
od 1926-01-01
PubMed
29301955
DOI
10.1104/pp.17.00925
Knihovny.cz E-zdroje
- MeSH
- Arabidopsis metabolismus MeSH
- endoplazmatické retikulum metabolismus MeSH
- membránové proteiny chemie metabolismus MeSH
- multimerizace proteinu * MeSH
- oxidoreduktasy chemie metabolismus MeSH
- proteinové domény MeSH
- proteiny - lokalizační signály MeSH
- proteiny huseníčku chemie metabolismus MeSH
- rekombinantní fúzní proteiny metabolismus MeSH
- sekvence aminokyselin MeSH
- stabilita proteinů MeSH
- zelené fluorescenční proteiny metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
Degradation of the plant hormone cytokinin is controlled by cytokinin oxidase/dehydrogenase (CKX) enzymes. The molecular and cellular behavior of these proteins is still largely unknown. In this study, we show that CKX1 is a type II single-pass membrane protein that localizes predominantly to the endoplasmic reticulum (ER) in Arabidopsis (Arabidopsis thaliana). This indicates that this CKX isoform is a bona fide ER protein directly controlling the cytokinin, which triggers the signaling from the ER. By using various approaches, we demonstrate that CKX1 forms homodimers and homooligomers in vivo. The amino-terminal part of CKX1 was necessary and sufficient for the protein oligomerization as well as for targeting and retention in the ER. Moreover, we show that protein-protein interaction is largely facilitated by transmembrane helices and depends on a functional GxxxG-like interaction motif. Importantly, mutations rendering CKX1 monomeric interfere with its steady-state localization in the ER and cause a loss of the CKX1 biological activity by increasing its ER-associated degradation. Therefore, our study provides evidence that oligomerization is a crucial parameter regulating CKX1 biological activity and the cytokinin concentration in the ER. The work also lends strong support for the cytokinin signaling from the ER and for the functional relevance of the cytokinin pool in this compartment.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19012947
- 003
- CZ-PrNML
- 005
- 20190405100542.0
- 007
- ta
- 008
- 190405s2018 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1104/pp.17.00925 $2 doi
- 035 __
- $a (PubMed)29301955
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Niemann, Michael C E $u Institute of Biology/Applied Genetics, Dahlem Centre of Plant Sciences, Freie Universität Berlin, D-14195 Berlin, Germany.
- 245 14
- $a The Cytokinin Oxidase/Dehydrogenase CKX1 Is a Membrane-Bound Protein Requiring Homooligomerization in the Endoplasmic Reticulum for Its Cellular Activity / $c MCE. Niemann, H. Weber, T. Hluska, G. Leonte, SM. Anderson, O. Novák, A. Senes, T. Werner,
- 520 9_
- $a Degradation of the plant hormone cytokinin is controlled by cytokinin oxidase/dehydrogenase (CKX) enzymes. The molecular and cellular behavior of these proteins is still largely unknown. In this study, we show that CKX1 is a type II single-pass membrane protein that localizes predominantly to the endoplasmic reticulum (ER) in Arabidopsis (Arabidopsis thaliana). This indicates that this CKX isoform is a bona fide ER protein directly controlling the cytokinin, which triggers the signaling from the ER. By using various approaches, we demonstrate that CKX1 forms homodimers and homooligomers in vivo. The amino-terminal part of CKX1 was necessary and sufficient for the protein oligomerization as well as for targeting and retention in the ER. Moreover, we show that protein-protein interaction is largely facilitated by transmembrane helices and depends on a functional GxxxG-like interaction motif. Importantly, mutations rendering CKX1 monomeric interfere with its steady-state localization in the ER and cause a loss of the CKX1 biological activity by increasing its ER-associated degradation. Therefore, our study provides evidence that oligomerization is a crucial parameter regulating CKX1 biological activity and the cytokinin concentration in the ER. The work also lends strong support for the cytokinin signaling from the ER and for the functional relevance of the cytokinin pool in this compartment.
- 650 _2
- $a sekvence aminokyselin $7 D000595
- 650 _2
- $a Arabidopsis $x metabolismus $7 D017360
- 650 _2
- $a proteiny huseníčku $x chemie $x metabolismus $7 D029681
- 650 _2
- $a endoplazmatické retikulum $x metabolismus $7 D004721
- 650 _2
- $a zelené fluorescenční proteiny $x metabolismus $7 D049452
- 650 _2
- $a membránové proteiny $x chemie $x metabolismus $7 D008565
- 650 _2
- $a oxidoreduktasy $x chemie $x metabolismus $7 D010088
- 650 _2
- $a proteinové domény $7 D000072417
- 650 12
- $a multimerizace proteinu $7 D055503
- 650 _2
- $a proteiny - lokalizační signály $7 D021382
- 650 _2
- $a stabilita proteinů $7 D055550
- 650 _2
- $a rekombinantní fúzní proteiny $x metabolismus $7 D011993
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a Research Support, N.I.H., Extramural $7 D052061
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Weber, Henriette $u Institute of Biology/Applied Genetics, Dahlem Centre of Plant Sciences, Freie Universität Berlin, D-14195 Berlin, Germany.
- 700 1_
- $a Hluska, Tomáš $u Department of Molecular Biology, Centre of the Region Haná for Biotechnological and Agricultural Research, Palacký University, 78371 Olomouc, Czech Republic.
- 700 1_
- $a Leonte, Georgeta $u Institute of Biology/Applied Genetics, Dahlem Centre of Plant Sciences, Freie Universität Berlin, D-14195 Berlin, Germany.
- 700 1_
- $a Anderson, Samantha M $u Department of Biochemistry, University of Wisconsin, Madison, Wisconsin 53706.
- 700 1_
- $a Novák, Ondřej $u Laboratory of Growth Regulators, Centre of the Region Haná for Biotechnological and Agricultural Research, Palacký University and Institute of Experimental Botany ASCR, 78371 Olomouc, Czech Republic.
- 700 1_
- $a Senes, Alessandro $u Department of Biochemistry, University of Wisconsin, Madison, Wisconsin 53706.
- 700 1_
- $a Werner, Tomáš $u Institute of Biology/Applied Genetics, Dahlem Centre of Plant Sciences, Freie Universität Berlin, D-14195 Berlin, Germany tomas.werner@uni-graz.at. Laboratory of Growth Regulators, Centre of the Region Haná for Biotechnological and Agricultural Research, Palacký University and Institute of Experimental Botany ASCR, 78371 Olomouc, Czech Republic. Institute of Plant Sciences, University of Graz, 8010 Graz, Austria.
- 773 0_
- $w MED00005317 $t Plant physiology $x 1532-2548 $g Roč. 176, č. 3 (2018), s. 2024-2039
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/29301955 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20190405 $b ABA008
- 991 __
- $a 20190405100551 $b ABA008
- 999 __
- $a ok $b bmc $g 1392257 $s 1051252
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2018 $b 176 $c 3 $d 2024-2039 $e 20180104 $i 1532-2548 $m Plant physiology $n Plant Physiol $x MED00005317
- LZP __
- $a Pubmed-20190405