Co-immunoprecipitation-based identification of putative BAX INHIBITOR-1-interacting proteins involved in cell death regulation and plant-powdery mildew interactions.
Co-immunoprecipitation-based identification of putative BAX INHIBITOR-1-interacting proteins involved in cell death regulation and plant-powdery mildew interactions.
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基于免疫共沉淀鉴定参与细胞死亡调节和植物-白粉病相互作用的推定 BAX INHIBITOR-1 相互作用蛋白
DOI:
10.1111/mpp.12050
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发表时间:
2013
影响因子:
4.9
通讯作者:
Hückelhoven R
中科院分区:
文献类型:
--
作者:
Weis C;Pfeilmeier S;Glawischnig E;Isono E;Pachl F;Hahne H;Kuster;Eichmann R;Hückelhoven R
The endoplasmic reticulum (ER)‐resident BAX INHIBITOR‐1 (BI‐1) protein is one of a few cell death suppressors known to be conserved in animals and plants. The function of BI‐1 proteins in response to various biotic and abiotic stress factors is well established. However, little is known about the underlying mechanisms. We conducted co‐immunoprecipitation (co‐IP) experiments to identifyArabidopsis thalianaBI‐1‐interacting proteins to obtain a potentially better understanding of how BI‐1 functions during plant–pathogen interactions and as a suppressor of cell death. Liquid chromatography and tandem mass spectrometry (LC‐MS/MS) identified 95 proteins co‐immunoprecipitated with green fluorescing protein (GFP)‐tagged BI‐1. Five selected candidate proteins, a RIBOPHORIN II (RPN2) family protein, VACUOLAR ATP SYNTHASE SUBUNIT A (VHA‐A), cytochrome P450 83A1 (CYP83A1), H+‐ATPASE 1 (AHA1) and PROHIBITIN 2 (PHB2), were further investigated with regard to their role in BI‐1‐associated processes. To this end, we analysed a set ofArabidopsismutants in the interaction with the adapted powdery mildew fungusErysiphe cruciferarumand on cell death‐inducing treatments. Two independentrpn2knock‐down mutants tended to better support powdery mildew, and aphb2mutant showed altered responses to cell death‐inducingAlternaria alternataf.sp.lycopersici(AAL) toxin treatment. Two independentcyp83a1mutants showed a strong powdery mildew resistance phenotype and enhanced sensitivity to AAL toxin. Moreover, co‐localization studies and fluorescence resonance energy transfer (FRET) experiments suggested a direct interaction of BI‐1 with CYP83A1 at the ER.
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DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
川合;ら
通讯作者:
ら
DOI:
10.1046/j.1365-313x.2000.00690.x
发表时间:
2000-02
期刊:
The Plant journal : for cell and molecular biology
影响因子:
--
作者:
Pedro Sanchez;Marta de Torres Zabala;Murray R Grant
通讯作者:
Pedro Sanchez;Marta de Torres Zabala;Murray R Grant
影响因子:
7.3
作者:
Bilodeau, P;Udvardi, MK;Dennis, ES
通讯作者:
Dennis, ES
影响因子:
7.4
作者:
Marco U. Reitz;Jeff Kweku Bissue;K. Zocher;A. Attard;R. Hückelhoven;K. Becker;J. Imani;R. Eichmann-R.-Eichma
通讯作者:
Marco U. Reitz;Jeff Kweku Bissue;K. Zocher;A. Attard;R. Hückelhoven;K. Becker;J. Imani;R. Eichmann-R.-Eichma
影响因子:
11.6
作者:
Kawai-Yamada, M;Ohori, Y;Uchimiya, H
通讯作者:
Uchimiya, H