Expressed sequence tags from Phytophthora sojae reveal genes specific to development and infection

被引:44
作者
Torto-Alalibo, Trudy A.
Tripathy, Sucheta
Smith, Brian M.
Arredondo, Felipe D.
Zhou, Lecong
Li, Hua
Chibucos, Marcus C.
Qutob, Dinah
Gijzen, Mark
Mao, Chunhong
Sobral, Bruno W. S.
Waugh, Mark E.
Mitchell, Thomas K.
Dean, Ralph A.
Tyler, Brett M. [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Virginia Bioinformat Inst, Blacksburg, VA 24061 USA
[2] Agr & Agri Food Canada, London, ON N5V 4T3, Canada
[3] Natl Ctr Genome Resources, Santa Fe, NM 87505 USA
[4] N Carolina State Univ, Ctr Integrated Fungal Res, Raleigh, NC 27695 USA
关键词
effectors;
D O I
10.1094/MPMI-20-7-0781
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Six unique expressed sequence tag (EST) libraries were generated from four developmental stages of Phytophthora sojae P6497. RNA was extracted from- mycelia, swimming zoospores, germinating cysts, and soybean (Glycine max (L.) Merr.) cv. Harosoy tissues heavily infected with R sojae. Three libraries were created from mycelia growing on defined medium, complex medium, and nutrient-limited medium. The 26,943 high-quality sequences obtained clustered into 7,863 unigenes composed of 2,845 contigs and 5,018 singletons. The total number of P sojae unigenes matching sequences in the genome assembly was 7,412 (94%). Of these unigenes, 7,088 (90%) matched gene models predicted from the P sojae sequence assembly, but only 2,047,(26%) matched R ramorum gene models. Analysis of EST frequency from different growth conditions and morphological stages revealed genes that were specific to or highly represented in particular growth conditions and life stages. Additionally, our results indicate that, during infection, the pathogen derives most of its carbon and energy via glycolysis of sugars in the plant. Sequences identified with]putative roles in pathogenesis included avirulence homologs possessing the RxLR motif, elicitins, and hydrolytic enzymes. This large collection of P sojae ESTs will serve as a valuable public genomic resource.
引用
收藏
页码:781 / 793
页数:13
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