a glutamic acid-rich protein identified in verticillium dahliae from an insertional mutagenesis affects microsclerotial formation and pathogenicity一个谷氨酸acid-rich蛋白质中确定黄萎病dahliae插入突变影响microsclerotial形成和致病性.pdfVIP
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a glutamic acid-rich protein identified in verticillium dahliae from an insertional mutagenesis affects microsclerotial formation and pathogenicity一个谷氨酸acid-rich蛋白质中确定黄萎病dahliae插入突变影响microsclerotial形成和致病性
A Glutamic Acid-Rich Protein Identified in Verticillium
dahliae from an Insertional Mutagenesis Affects
Microsclerotial Formation and Pathogenicity
1,2. 1,3. 2 2 2 1,3 1,3
Feng Gao , Bang-Jun Zhou , Guo-Ying Li , Pei-Song Jia , Hui Li , Yun-Long Zhao , Pan Zhao ,
1 1
Gui-Xian Xia , Hui-Shan Guo *
1 State Key Laboratory of Plant Genomics and National Center for Plant Gene Research (Beijing), Institute of Microbiology, Chinese Academy of Sciences, Beijing, China,
2 The Key Laboratory of Prevention and Control for Oasis Crop Disease, Shihezi University, Shihezi, Xinjiang, China, 3 Graduate University of Chinese Academy of Sciences,
Beijing, China
Abstract
Verticillium dahliae Kleb. is a phytopathogenic fungus that causes wilt disease in a wide range of crops, including cotton.
The life cycle of V. dahliae includes three vegetative phases: parasitic, saprophytic and dormant. The dormant microsclerotia
are the primary infectious propagules, which germinate when they are stimulated by root exudates. In this study, we report
the first application of Agrobacterium tumefaciens-mediated transformation (ATMT) for construction of insertional mutants
from a virulent defoliating isolate of V. dahliae (V592). Changes in morphology, especially a lack of melanized microsclerotia
or pigmentation traits, were observed in mutants. Together with the established laboratory unimpaired root dip-inoculation
approach, we found insertional mutants to be affected in their pathogenicities in cotton. One of the genes tagged in a
pathogenicity mutant encoded a glutamic acid-rich protein (VdGARP1), which shared no significant similarity to any known
annotated gene. The
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