Sequence mining and transcript profiling to explore cyst nematode parasitism

被引:36
作者
Elling, Axel A. [1 ,2 ,3 ]
Mitreva, Makedonka [4 ]
Gai, Xiaowu [5 ]
Martin, John [4 ]
Recknor, Justin [6 ,7 ]
Davis, Eric L. [8 ]
Hussey, Richard S. [9 ]
Nettleton, Dan [6 ]
McCarter, James P. [4 ,10 ]
Baum, Thomas J. [1 ,2 ]
机构
[1] Iowa State Univ, Interdepartmental Genet Program, Ames, IA 50011 USA
[2] Iowa State Univ, Dept Plant Pathol, Ames, IA 50011 USA
[3] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[4] Washington Univ, Dept Genet, Genome Sequencing Ctr, Sch Med, St Louis, MO 63108 USA
[5] Childrens Hosp Philadelphia, Ctr Biomed Informat, Philadelphia, PA 19104 USA
[6] Iowa State Univ, Dept Stat, Ames, IA 50011 USA
[7] Eli Lilly & Co, Lilly Res Labs, Greenfield, IN 46140 USA
[8] N Carolina State Univ, Dept Plant Pathol, Raleigh, NC 27695 USA
[9] Univ Georgia, Dept Plant Pathol, Athens, GA 30602 USA
[10] Divergence Inc, St Louis, MO 63141 USA
来源
BMC GENOMICS | 2009年 / 10卷
关键词
ESOPHAGEAL GLAND-CELLS; LIFE-CYCLE STAGES; ART; NO; R39; HETERODERA-GLYCINES; GENE-EXPRESSION; DEVELOPMENTAL EXPRESSION; CAENORHABDITIS-ELEGANS; HISTONE MODIFICATIONS; TRICHINELLA-SPIRALIS; ARABIDOPSIS-THALIANA;
D O I
10.1186/1471-2164-10-58
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Cyst nematodes are devastating plant parasites that become sedentary within plant roots and induce the transformation of normal plant cells into elaborate feeding cells with the help of secreted effectors, the parasitism proteins. These proteins are the translation products of parasitism genes and are secreted molecular tools that allow cyst nematodes to infect plants. Results: We present here the expression patterns of all previously described parasitism genes of the soybean cyst nematode, Heterodera glycines, in all major life stages except the adult male. These insights were gained by analyzing our gene expression dataset from experiments using the Affymetrix Soybean Genome Array GeneChip, which contains probeset sequences for 6,860 genes derived from preparasitic and parasitic H. glycines life stages. Targeting the identification of additional H. glycines parasitism-associated genes, we isolated 633 genes encoding secretory proteins using algorithms to predict secretory signal peptides. Furthermore, because some of the known H. glycines parasitism proteins have strongest similarity to proteins of plants and microbes, we searched for predicted protein sequences that showed their highest similarities to plant or microbial proteins and identified 156 H. glycines genes, some of which also contained a signal peptide. Analyses of the expression profiles of these genes allowed the formulation of hypotheses about potential roles in parasitism. This is the first study combining sequence analyses of a substantial EST dataset with microarray expression data of all major life stages (except adult males) for the identification and characterization of putative parasitism-associated proteins in any parasitic nematode. Conclusion: We have established an expression atlas for all known H. glycines parasitism genes. Furthermore, in an effort to identify additional H. glycines genes with putative functions in parasitism, we have reduced the currently known 6,860 H. glycines genes to a pool of 788 most promising candidate genes (including known parasitism genes) and documented their expression profiles. Using our approach to pre-select genes likely involved in parasitism now allows detailed functional analyses in a manner not feasible for larger numbers of genes. The generation of the candidate pool described here is an important enabling advance because it will significantly facilitate the unraveling of fascinating plant-animal interactions and deliver knowledge that can be transferred to other pathogen-host systems. Ultimately, the exploration of true parasitism genes verified from the gene pool delineated here will identify weaknesses in the nematode life cycle that can be exploited by novel anti-nematode efforts.
引用
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页数:17
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