Cloning and characterization of genes specifically expressed during infection stages in the rice blast fungus

被引:20
作者
Banno, S
Kimura, M
Tokai, T
Kasahara, S
Higa-Nishiyama, A
Takahashi-Ando, N
Hamamoto, H
Fujimura, M
Staskawicz, BJ
Yamaguchi, I
机构
[1] RIKEN, Lab Remediat Res, Plant Sci Ctr, Wako, Saitama 3510198, Japan
[2] Toyo Univ, Dept Life Sci, Itakura, Gunma 3740193, Japan
[3] Univ Calif Berkeley, Dept Plant & Microbial Biol, Berkeley, CA 94720 USA
[4] RIKEN, Lab Adaptat & Resistance, Plant Sci Ctr, Yokohama, Kanagawa 2300045, Japan
关键词
expressed sequence tag; fungal differentiation; green fluorescence protein; promoter-egfp fusion; targeted gene disruption; vectorette polymerase chain reaction;
D O I
10.1016/S0378-1097(03)00307-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We isolated promoters of 12 genes from the rice blast fungus based on the sequences of randomly selected expressed sequence tags (ESTs) (appressorium formation stage cDNA library of Magnaporthe available from GenBank). These promoters (and the 5' coding regions if any) were fused in frame with egfp, and their expression patterns were examined under the epifluorescence microscope. Among them, two turned out to be specifically active in structures necessary for infection, viz. a promoter of adenylate cyclase interacting protein I-like gene expressed in conidia, germ tubes, and appressoria, and a promoter of putative membrane-associated or secreted protein gene specifically expressed in appressoria. Although targeted knockout mutants of either gene failed to show detectable phenotypic alterations under laboratory conditions, these ESTs should be useful for identification of genes expressed during infection stages. (C) 2003 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:221 / 227
页数:7
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