Identification and expression analysis of EDR1-like genes in tobacco (Nicotiana tabacum) in response to Golovinomyces orontii
Author(s) -
Lei Wu,
Xiaoying Zhang,
Bingxin Xu,
Yueyue Li,
Ling Jia,
Rengang Wang,
Xueliang Ren,
Genhong Wang,
Qingyou Xia
Publication year - 2018
Publication title -
peerj
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.927
H-Index - 70
ISSN - 2167-8359
DOI - 10.7717/peerj.5244
Subject(s) - powdery mildew , nicotiana tabacum , biology , gene , nicotiana , arabidopsis , genetics , plant disease resistance , botany , gene family , gene expression , solanaceae , mutant
ENHANCED DISEASE RESISTANCE1 ( EDR1 ) encodes a Raf -like mitogen-activated protein kinase, and it acts as a negative regulator of disease resistance and ethylene-induced senescence. Mutations in the EDR1 gene can enhance resistance to powdery mildew both in monocotyledonous and dicotyledonous plants. However, little is known about EDR1 -like gene members from a genome-wide perspective in plants. In this study, the tobacco (Nicotiana tabacum) EDR1 -like gene family was first systematically analyzed. We identified 19 EDR1 -like genes in tobacco, and compared them to those from Arabidopsis, tomato and rice. Phylogenetic analyses divided the EDR1 -like gene family into six clades, among them monocot and dicot plants were respectively divided into two sub-clades. NtEDR1-1A and NtEDR1-1B were classified into clade I in which the other members have been reported to negatively regulate plant resistance to powdery mildew. The expression patterns of tobacco EDR1 -like genes were analyzed after plants were challenged by Golovinomyces orontii , and showed that several other EDR1 -like genes were induced after infection, as well as NtEDR1-1A and NtEDR1-1B . Expression analysis showed that NtEDR1-13 and NtEDR1-16 had exclusively abundant expression patterns in roots and leaves, respectively, and the remaining NtEDR1 -like members were actively expressed in most of the tissue/organ samples investigated. Our findings will contribute to further study of the physiological functions of EDR1 -like genes in tobacco.
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