-
Je něco špatně v tomto záznamu ?
Phosphoproteomics Profiling of Tobacco Mature Pollen and Pollen Activated in vitro
J. Fíla, S. Radau, A. Matros, A. Hartmann, U. Scholz, J. Feciková, HP. Mock, V. Čapková, RP. Zahedi, D. Honys,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 2002 do Před 1 rokem
Freely Accessible Science Journals
od 2002
PubMed Central
od 2008
Europe PubMed Central
od 2008 do Před 1 rokem
Open Access Digital Library
od 2002-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2002
PubMed
26792808
DOI
10.1074/mcp.m115.051672
Knihovny.cz E-zdroje
- MeSH
- fosfoproteiny chemie metabolismus MeSH
- kinetika MeSH
- proteomika metody MeSH
- pyl metabolismus MeSH
- regulace genové exprese u rostlin MeSH
- rostlinné proteiny chemie metabolismus MeSH
- tabák genetika metabolismus MeSH
- tandemová hmotnostní spektrometrie metody MeSH
- vazebná místa MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Tobacco mature pollen has extremely desiccated cytoplasm, and is metabolically quiescent. Upon re-hydration it becomes metabolically active and that results in later emergence of rapidly growing pollen tube. These changes in cytoplasm hydration and metabolic activity are accompanied by protein phosphorylation. In this study, we subjected mature pollen, 5-min-activated pollen, and 30-min-activated pollen to TCA/acetone protein extraction, trypsin digestion and phosphopeptide enrichment by titanium dioxide. The enriched fraction was subjected to nLC-MS/MS. We identified 471 phosphopeptides that carried 432 phosphorylation sites, position of which was exactly matched by mass spectrometry. These 471 phosphopeptides were assigned to 301 phosphoproteins, because some proteins carried more phosphorylation sites. Of the 13 functional groups, the majority of proteins were put into these categories: transcription, protein synthesis, protein destination and storage, and signal transduction. Many proteins were of unknown function, reflecting the fact that male gametophyte contains many specific proteins that have not been fully functionally annotated. The quantitative data highlighted the dynamics of protein phosphorylation during pollen activation; the identified phosphopeptides were divided into seven groups based on the regulatory trends. The major group comprised mature pollen-specific phosphopeptides that were dephosphorylated during pollen activation. Several phosphopeptides representing the same phosphoprotein had different regulation, which pinpointed the complexity of protein phosphorylation and its clear functional context. Collectively, we showed the first phosphoproteomics data on activated pollen where the position of phosphorylation sites was clearly demonstrated and regulatory kinetics was resolved.
§Leibniz Institut für Analytische Wissenschaften ISAS e 5 Otto Hahn Straβe 6b 44227 Dortmund Germany
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc17000608
- 003
- CZ-PrNML
- 005
- 20170119121836.0
- 007
- ta
- 008
- 170103s2016 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1074/mcp.M115.051672 $2 doi
- 024 7_
- $a 10.1074/mcp.M115.051672 $2 doi
- 035 __
- $a (PubMed)26792808
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Fíla, Jan $u From the ‡Laboratory of Pollen Biology, Institute of Experimental Botany ASCR, v.v.i., Rozvojova 263, 165 00 Praha 6, Czech Republic;
- 245 10
- $a Phosphoproteomics Profiling of Tobacco Mature Pollen and Pollen Activated in vitro / $c J. Fíla, S. Radau, A. Matros, A. Hartmann, U. Scholz, J. Feciková, HP. Mock, V. Čapková, RP. Zahedi, D. Honys,
- 520 9_
- $a Tobacco mature pollen has extremely desiccated cytoplasm, and is metabolically quiescent. Upon re-hydration it becomes metabolically active and that results in later emergence of rapidly growing pollen tube. These changes in cytoplasm hydration and metabolic activity are accompanied by protein phosphorylation. In this study, we subjected mature pollen, 5-min-activated pollen, and 30-min-activated pollen to TCA/acetone protein extraction, trypsin digestion and phosphopeptide enrichment by titanium dioxide. The enriched fraction was subjected to nLC-MS/MS. We identified 471 phosphopeptides that carried 432 phosphorylation sites, position of which was exactly matched by mass spectrometry. These 471 phosphopeptides were assigned to 301 phosphoproteins, because some proteins carried more phosphorylation sites. Of the 13 functional groups, the majority of proteins were put into these categories: transcription, protein synthesis, protein destination and storage, and signal transduction. Many proteins were of unknown function, reflecting the fact that male gametophyte contains many specific proteins that have not been fully functionally annotated. The quantitative data highlighted the dynamics of protein phosphorylation during pollen activation; the identified phosphopeptides were divided into seven groups based on the regulatory trends. The major group comprised mature pollen-specific phosphopeptides that were dephosphorylated during pollen activation. Several phosphopeptides representing the same phosphoprotein had different regulation, which pinpointed the complexity of protein phosphorylation and its clear functional context. Collectively, we showed the first phosphoproteomics data on activated pollen where the position of phosphorylation sites was clearly demonstrated and regulatory kinetics was resolved.
- 650 _2
- $a vazebná místa $7 D001665
- 650 _2
- $a regulace genové exprese u rostlin $7 D018506
- 650 _2
- $a kinetika $7 D007700
- 650 _2
- $a fosfoproteiny $x chemie $x metabolismus $7 D010750
- 650 _2
- $a rostlinné proteiny $x chemie $x metabolismus $7 D010940
- 650 _2
- $a pyl $x metabolismus $7 D011058
- 650 _2
- $a proteomika $x metody $7 D040901
- 650 _2
- $a tandemová hmotnostní spektrometrie $x metody $7 D053719
- 650 _2
- $a tabák $x genetika $x metabolismus $7 D014026
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Radau, Sonja $u §Leibniz-Institut für Analytische Wissenschaften-ISAS-e.V., Otto-Hahn-Straβe 6b, 44227 Dortmund, Germany;
- 700 1_
- $a Matros, Andrea $u ¶Department of Physiology and Cell Biology, Leibniz Institute of Plant Genetic and Crop Plant Research, Corrensstraβe 3, 06466 Gatersleben, Germany;
- 700 1_
- $a Hartmann, Anja $u ¶Department of Physiology and Cell Biology, Leibniz Institute of Plant Genetic and Crop Plant Research, Corrensstraβe 3, 06466 Gatersleben, Germany;
- 700 1_
- $a Scholz, Uwe $u ‖Department of Breeding Research, Leibniz Institute of Plant Genetic and Crop Plant Research, Corrensstraβe 3, 06466 Gatersleben, Germany.
- 700 1_
- $a Feciková, Jana $u From the ‡Laboratory of Pollen Biology, Institute of Experimental Botany ASCR, v.v.i., Rozvojova 263, 165 00 Praha 6, Czech Republic;
- 700 1_
- $a Mock, Hans-Peter $u ¶Department of Physiology and Cell Biology, Leibniz Institute of Plant Genetic and Crop Plant Research, Corrensstraβe 3, 06466 Gatersleben, Germany;
- 700 1_
- $a Čapková, Věra $u From the ‡Laboratory of Pollen Biology, Institute of Experimental Botany ASCR, v.v.i., Rozvojova 263, 165 00 Praha 6, Czech Republic;
- 700 1_
- $a Zahedi, René Peiman $u §Leibniz-Institut für Analytische Wissenschaften-ISAS-e.V., Otto-Hahn-Straβe 6b, 44227 Dortmund, Germany;
- 700 1_
- $a Honys, David $u From the ‡Laboratory of Pollen Biology, Institute of Experimental Botany ASCR, v.v.i., Rozvojova 263, 165 00 Praha 6, Czech Republic; david@ueb.cas.cz.
- 773 0_
- $w MED00007436 $t Molecular & cellular proteomics MCP $x 1535-9484 $g Roč. 15, č. 4 (2016), s. 1338-50
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/26792808 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20170103 $b ABA008
- 991 __
- $a 20170119121945 $b ABA008
- 999 __
- $a ok $b bmc $g 1179748 $s 961175
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2016 $b 15 $c 4 $d 1338-50 $e 20160120 $i 1535-9484 $m Molecular and cellular proteomics $n Mol Cell Proteomics $x MED00007436
- LZP __
- $a Pubmed-20170103