Regulation of the microsomal proteome by salicylic acid and deficiency of phosphatidylinositol-4-kinases beta 1 and beta 2 in Arabidopsis thaliana
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22330%2F21%3A43922233" target="_blank" >RIV/60461373:22330/21:43922233 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/60076658:12310/21:43906089
Výsledek na webu
<a href="https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/epdf/10.1002/pmic.202000223" target="_blank" >https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/epdf/10.1002/pmic.202000223</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/pmic.202000223" target="_blank" >10.1002/pmic.202000223</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Regulation of the microsomal proteome by salicylic acid and deficiency of phosphatidylinositol-4-kinases beta 1 and beta 2 in Arabidopsis thaliana
Popis výsledku v původním jazyce
Phosphatidylinositol-4-kinases beta 1 and beta 2 (PI4K beta 1/PI4K beta 2), which are responsible for phosphorylation of phosphatidylinositol to phosphatidylinositol-4-phosphate, have important roles in plant vesicular trafficking. Moreover, PI4K beta 1/PI4K beta 2 negatively regulates biosynthesis of phytohormone salicylic acid (SA), a key player in plant immune responses. The study focused on the effect of PI4K beta 1/PI4K beta 2 deficiency and SA level on the proteome of microsomal fraction. For that purpose we used four Arabidopsis thaliana genotypes: wild type; double mutant with impaired function of PI4K beta 1/PI4K beta 2 (pi4k beta 1/pi4k beta 2) exhibiting high SA level; sid2 mutant with impaired SA biosynthesis depending on the isochorismate synthase 1 and triple mutant sid2/pi4k beta 1/pi4k beta 2. We identified 1797 proteins whose levels were changed between genotypes. We showed that increased SA concentration affected the levels of 473 proteins. This includes typical SA pathway markers but also points to connections between SA pathway and clathrin-independent endocytosis (flotillins) and exocytosis/protein secretion (syntaxins, tetraspanin) to be investigated in future. In contrast to SA, the absence of PI4K beta 1/PI4K beta 2 itself affected only 27 proteins. Among them we identified CERK1, a receptor for chitin. Although PI4K beta 1/PI4K beta 2 deficiency itself did not have a substantial impact on the proteome of the microsomal fraction, our data clearly show that it enhances proteome changes when SA pathway is modulated in parallel.
Název v anglickém jazyce
Regulation of the microsomal proteome by salicylic acid and deficiency of phosphatidylinositol-4-kinases beta 1 and beta 2 in Arabidopsis thaliana
Popis výsledku anglicky
Phosphatidylinositol-4-kinases beta 1 and beta 2 (PI4K beta 1/PI4K beta 2), which are responsible for phosphorylation of phosphatidylinositol to phosphatidylinositol-4-phosphate, have important roles in plant vesicular trafficking. Moreover, PI4K beta 1/PI4K beta 2 negatively regulates biosynthesis of phytohormone salicylic acid (SA), a key player in plant immune responses. The study focused on the effect of PI4K beta 1/PI4K beta 2 deficiency and SA level on the proteome of microsomal fraction. For that purpose we used four Arabidopsis thaliana genotypes: wild type; double mutant with impaired function of PI4K beta 1/PI4K beta 2 (pi4k beta 1/pi4k beta 2) exhibiting high SA level; sid2 mutant with impaired SA biosynthesis depending on the isochorismate synthase 1 and triple mutant sid2/pi4k beta 1/pi4k beta 2. We identified 1797 proteins whose levels were changed between genotypes. We showed that increased SA concentration affected the levels of 473 proteins. This includes typical SA pathway markers but also points to connections between SA pathway and clathrin-independent endocytosis (flotillins) and exocytosis/protein secretion (syntaxins, tetraspanin) to be investigated in future. In contrast to SA, the absence of PI4K beta 1/PI4K beta 2 itself affected only 27 proteins. Among them we identified CERK1, a receptor for chitin. Although PI4K beta 1/PI4K beta 2 deficiency itself did not have a substantial impact on the proteome of the microsomal fraction, our data clearly show that it enhances proteome changes when SA pathway is modulated in parallel.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10608 - Biochemistry and molecular biology
Návaznosti výsledku
Projekt
<a href="/cs/project/GA17-05151S" target="_blank" >GA17-05151S: Enzymy metabolizující fosfolipidy jako nové komponenty signální dráhy kyseliny salicylové</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2021
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Proteomics
ISSN
1615-9853
e-ISSN
—
Svazek periodika
21
Číslo periodika v rámci svazku
5
Stát vydavatele periodika
DE - Spolková republika Německo
Počet stran výsledku
6
Strana od-do
—
Kód UT WoS článku
000620571400001
EID výsledku v databázi Scopus
2-s2.0-85101281948