Characterization of cell death inducing Phytophthora capsici CRN effectors suggests diverse activities in the host nucleus.
Characterization of cell death inducing Phytophthora capsici CRN effectors suggests diverse activities in the host nucleus.
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细胞死亡的表征诱导植物膜状CRN效应子表明宿主核中的活性各不相同。
DOI:
10.3389/fpls.2013.00387
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发表时间:
2013
影响因子:
5.6
通讯作者:
Huitema E
中科院分区:
文献类型:
--
作者:
Stam R;Howden AJ;Delgado-Cerezo M;M M Amaro TM;Motion GB;Pham J;Huitema E
Plant-Microbe interactions are complex associations that feature recognition of Pathogen Associated Molecular Patterns by the plant immune system and dampening of subsequent responses by pathogen encoded secreted effectors. With large effector repertoires now identified in a range of sequenced microbial genomes, much attention centers on understanding their roles in immunity or disease. These studies not only allow identification of pathogen virulence factors and strategies, they also provide an important molecular toolset suited for studying immunity in plants. The Phytophthora intracellular effector repertoire encodes a large class of proteins that translocate into host cells and exclusively target the host nucleus. Recent functional studies have implicated the CRN protein family as an important class of diverse effectors that target distinct subnuclear compartments and modify host cell signaling. Here, we characterized three necrosis inducing CRNs and show that there are differences in the levels of cell death. We show that only expression of CRN20_624 has an additive effect on PAMP induced cell death but not AVR3a induced ETI. Given their distinctive phenotypes, we assessed localization of each CRN with a set of nuclear markers and found clear differences in CRN subnuclear distribution patterns. These assays also revealed that expression of CRN83_152 leads to a distinct change in nuclear chromatin organization, suggesting a distinct series of events that leads to cell death upon over-expression. Taken together, our results suggest diverse functions carried by CRN C-termini, which can be exploited to identify novel processes that take place in the host nucleus and are required for immunity or susceptibility.
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影响因子:
12.3
作者:
Jupe J;Stam R;Howden AJ;Morris JA;Zhang R;Hedley PE;Huitema E
通讯作者:
Huitema E
影响因子:
12.3
作者:
Lévesque CA;Brouwer H;Cano L;Hamilton JP;Holt C;Huitema E;Raffaele S;Robideau GP;Thines M;Win J;Zerillo MM;Beakes GW;Boore JL;Busam D;Dumas B;Ferriera S;Fuerstenberg SI;Gachon CM;Gaulin E;Govers F;Grenville-Briggs L;Horner N;Hostetler J;Jiang RH;Johnson J;Krajaejun T;Lin H;Meijer HJ;Moore B;Morris P;Phuntmart V;Puiu D;Shetty J;Stajich JE;Tripathy S;Wawra S;van West P;Whitty BR;Coutinho PM;Henrissat B;Martin F;Thomas PD;Tyler BM;De Vries RP;Kamoun S;Yandell M;Tisserat N;Buell CR
通讯作者:
Buell CR
影响因子:
11.6
作者:
Dou, Daolong;Kale, Shiv D.;Tyler, Brett M.
通讯作者:
Tyler, Brett M.
影响因子:
3.7
作者:
Gaulin E;Madoui MA;Bottin A;Jacquet C;Mathé C;Couloux A;Wincker P;Dumas B
通讯作者:
Dumas B
影响因子:
3.5
作者:
Bos, Jorunn I. B.;Chaparro-Garcia, Angela;Kamoun, Sophien
通讯作者:
Kamoun, Sophien