Analysis of expressed sequence tags from cDNA library of Fusarium culmorum infected barley (Hordeum vulgare L.) roots

被引:4
|
作者
Tufan, Feyza [1 ]
Ucarli, Cuneyt [1 ]
Gurel, Filiz [1 ,2 ]
机构
[1] Istanbul Univ, Dept Mol Biol & Genet, Fac Sci, TR-34134 Istanbul, Turkey
[2] Istanbul Univ, Res & Applicat Ctr Biotechnol & Genet Engn, TR-34134 Istanbul, Turkey
关键词
barley; ESTs; root rot and crown rot diseases; Fusarium culmorum;
D O I
10.6026/97320630011034
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fusarium culmorum is one of the most common and globally important causal agent of root and crown rot diseases of cereals. These diseases cause grain yield loss and reduced grain quality in barley. In this study, we have analyzed an expressed sequence tag (EST) database derived from F. culmorum infected barley root tissues available at the National Center for Biotechnology Information (NCBI). The 2294 sequences were assembled into 1619 non-redundant sequences consisting of 359 contigs and 1260 singletons using the program CAPS. BLASTX analysis for these sequences was conducted in order to find similar sequences in all databases. Gene Ontology search, enzyme search, KEGG mapping and InterProScan search were done using Blast2GO 3.0.7 tool. By BLASTX analysis, 41.7%, 7.7%, 3.2% and 47.4% of ESTs were categorized as annotated, unannotated, not mapping and without blast hits, respectively. BLASTX analysis revealed that the majority of top hits were barley proteins (43.5%). Based on Gene Ontology classification, 38.3%, 31.3%, and 16% of ESTs were assigned to molecular function, biological process, and cellular component GO terms, respectively. Most abundant GO terms were as follows: 157 sequences were related to response to stress (biological process), 207 sequences were related to ion binding (molecular function), and 160 sequences were related to plastid (cellular component). Furthermore, based on KEGG mapping, 369 sequences could be assigned to 264 enzymes and 83 different KEGG pathways. According to Enzyme Commission (EC) distribution; 94 sequences were transferases (EC2) while 70 sequences were hydrolases (EC3).
引用
收藏
页码:34 / 38
页数:5
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