The Arabidopsis Mediator complex subunits MED14/SWP and MED16/SFR6/IEN1 differentially regulate defense gene expression in plant immune responses

被引:73
作者
Zhang, Xudong [1 ]
Yao, Jin [2 ]
Zhang, Yanping [3 ]
Sun, Yijun [2 ]
Mou, Zhonglin [1 ]
机构
[1] Univ Florida, Dept Microbiol & Cell Sci, Gainesville, FL 32611 USA
[2] SUNY Buffalo, Dept Microbiol & Immunol, Buffalo, NY 14203 USA
[3] Univ Florida, Interdisciplinary Ctr Biotechnol Res, Gainesville, FL 32610 USA
基金
美国国家科学基金会;
关键词
MED14; NPR1; plant immunity; salicylic acid; systemic acquired resistance; gene transcription; Arabidopsis thaliana; SYSTEMIC ACQUIRED-RESISTANCE; SALICYLIC-ACID; FUNCTIONAL-ANALYSIS; DISEASE RESISTANCE; TRANSCRIPTION; JASMONATE; THALIANA; PROTEIN; NPR1; ACTIVATION;
D O I
10.1111/tpj.12216
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Pathogen infection in plants triggers large-scale transcriptional changes, both locally and systemically. Emerging evidence suggests that the Arabidopsis Mediator complex plays a crucial role in these transcriptional changes. Mediator is highly conserved in eukaryotes, and its core comprises more than 20 subunits organized into three modules named head, middle and tail. The head and middle modules interact with general transcription factors and RNA polymeraseII, whereas the tail module associates with activators, and signals through the head and middle modules to the basal transcription machinery. In Arabidopsis, three tail module subunits, MED14, MED15 and MED16, have been identified. Both MED15 and MED16 have been implicated in plant immunity, but the role of MED14 has not been established. Here, we report the characterization of an Arabidopsis T-DNA insertion mutant of the MED14 gene. Similarly to the med15 and/or med16 mutations, the med14 mutation significantly suppresses salicylic acid-induced defense responses, alters transcriptional changes induced by the avirulent bacterial pathogen Pseudomonas syringae pv. tomato (Pst) DC3000/avrRpt2, and renders plants susceptible to both Pst DC3000/avrRpt2 and Pst DC3000. The med14 mutation also completely compromises biological induction of systemic acquired resistance (SAR), indicating that the tail module as a whole is essential for SAR. Interestingly, unlike the med16 mutation, which differentially affects expression of several SAR positive and negative regulators, med14 inhibits induction of a large group of defense genes, including both SAR positive and negative regulators, suggesting that individual subunits of the Mediator tail module employ distinct mechanisms to regulate plant immune responses.
引用
收藏
页码:484 / 497
页数:14
相关论文
共 80 条
[61]   A high-throughput Arabidopsis reverse genetics system [J].
Sessions, A ;
Burke, E ;
Presting, G ;
Aux, G ;
McElver, J ;
Patton, D ;
Dietrich, B ;
Ho, P ;
Bacwaden, J ;
Ko, C ;
Clarke, JD ;
Cotton, D ;
Bullis, D ;
Snell, J ;
Miguel, T ;
Hutchison, D ;
Kimmerly, B ;
Mitzel, T ;
Katagiri, F ;
Glazebrook, J ;
Law, M ;
Goff, SA .
PLANT CELL, 2002, 14 (12) :2985-2994
[62]   Characterization of a salicylic acid-insensitive mutant (sai1) of Arabidopsis thaliana, identified in a selective screen utilizing the SA-inducible expression of the tms2 gene [J].
Shah, J ;
Tsui, F ;
Klessig, DF .
MOLECULAR PLANT-MICROBE INTERACTIONS, 1997, 10 (01) :69-78
[63]   DNA Repair Proteins Are Directly Involved in Regulation of Gene Expression during Plant Immune Response [J].
Song, Junqi ;
Durrant, Wendy E. ;
Wang, Shui ;
Yan, Shunping ;
Tan, Ek Han ;
Dong, Xinnian .
CELL HOST & MICROBE, 2011, 9 (02) :115-124
[64]   A direct approach to false discovery rates [J].
Storey, JD .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 2002, 64 :479-498
[65]   Mediator as a general transcription factor [J].
Takagi, Y ;
Kornberg, RD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (01) :80-89
[66]   Human Mediator Subunit MED26 Functions as a Docking Site for Transcription Elongation Factors [J].
Takahashi, Hidehisa ;
Parmely, Tari J. ;
Sato, Shigeo ;
Tomomori-Sato, Chieri ;
Banks, Charles A. S. ;
Kong, Stephanie E. ;
Szutorisz, Henrietta ;
Swanson, Selene K. ;
Martin-Brown, Skylar ;
Washburn, Michael P. ;
Florens, Laurence ;
Seidel, Chris W. ;
Lin, Chengqi ;
Smith, Edwin R. ;
Shilatifard, Ali ;
Conaway, Ronald C. ;
Conaway, Joan W. .
CELL, 2011, 146 (01) :92-104
[67]   Quantitative nature of Arabidopsis responses during compatible and incompatible interactions with the bacterial pathogen Pseudomonas syringae [J].
Tao, Y ;
Xie, ZY ;
Chen, WQ ;
Glazebrook, J ;
Chang, HS ;
Han, B ;
Zhu, T ;
Zou, GZ ;
Katagiri, F .
PLANT CELL, 2003, 15 (02) :317-330
[68]   Fusarium oxysporum hijacks COI1-mediated jasmonate signaling to promote disease development in Arabidopsis [J].
Thatcher, Louise F. ;
Manners, John M. ;
Kazan, Kemal .
PLANT JOURNAL, 2009, 58 (06) :927-939
[69]   Method for the extraction of the volatile compound salicylic acid from tobacco leaf material [J].
Verberne, MC ;
Brouwer, N ;
Delbianco, F ;
Linthorst, HJM ;
Bol, JF ;
Verpoorte, R .
PHYTOCHEMICAL ANALYSIS, 2002, 13 (01) :45-50
[70]   Non-Recognition-of-BTH4, an Arabidopsis Mediator Subunit Homolog, Is Necessary for Development and Response to Salicylic Acid [J].
Vicente Canet, Juan ;
Dobon, Albor ;
Tornero, Pablo .
PLANT CELL, 2012, 24 (10) :4220-4235