TY - JOUR
T1 - Detection of putative secreted proteins in the plant-parasitic nematode Heterodera schachtii
AU - Vanholme, Bartel
AU - Mitreva, Makedonka
AU - Van Criekinge, Wim
AU - Logghe, Marc
AU - Bird, David
AU - McCarter, James P.
AU - Gheysen, Godelieve
N1 - Funding Information:
Acknowledgments We thank Claire Murphy and Mike Dante for their role in library generation and technical support. H. schachtii EST sequencing was supported by a US National Science Foundation Plant Genome Award 0077503 to D.B. of North Carolina State University and Sandra Clifton of Washington University. Research at Ghent University was supported by the European Union (NONEMA EC, QLT-CT 1999-01501) and the Fund for Scientific Research-Flanders.
PY - 2006/4
Y1 - 2006/4
N2 - The beet cyst nematode Heterodera schachtii is an important pathogen worldwide, but its molecular characterization has been limited to studying individual genes of interest. We undertook a high-throughput genomic approach and drastically increased the number of available sequences for this parasite. A total of 2,662 expressed sequence tags were grouped into 1,212 clusters representing a nonredundant catalog of H. schachtii genes. Implementing a bioinformatic workflow, we identified 50 sequences coding for candidate secreted proteins. All of these contain a putative signal peptide required for entry into the secretory pathway and lack any transmembrane domain. Included are previously postulated cell-wall-degrading enzymes and other parasitism-related genes. Moreover, we provide the first report of an arabinogalactan endo-1,4-β-galactosidase enzyme (EC 3.2.1.89) in animals. As sequence data increase at a rapid rate, developing high-throughput genomic screening is a necessity. The in silico approach described here is an effective way to identify putative secreted proteins and prioritize candidates for further studies.
AB - The beet cyst nematode Heterodera schachtii is an important pathogen worldwide, but its molecular characterization has been limited to studying individual genes of interest. We undertook a high-throughput genomic approach and drastically increased the number of available sequences for this parasite. A total of 2,662 expressed sequence tags were grouped into 1,212 clusters representing a nonredundant catalog of H. schachtii genes. Implementing a bioinformatic workflow, we identified 50 sequences coding for candidate secreted proteins. All of these contain a putative signal peptide required for entry into the secretory pathway and lack any transmembrane domain. Included are previously postulated cell-wall-degrading enzymes and other parasitism-related genes. Moreover, we provide the first report of an arabinogalactan endo-1,4-β-galactosidase enzyme (EC 3.2.1.89) in animals. As sequence data increase at a rapid rate, developing high-throughput genomic screening is a necessity. The in silico approach described here is an effective way to identify putative secreted proteins and prioritize candidates for further studies.
UR - http://www.scopus.com/inward/record.url?scp=33645243360&partnerID=8YFLogxK
U2 - 10.1007/s00436-005-0029-3
DO - 10.1007/s00436-005-0029-3
M3 - Article
C2 - 16380840
AN - SCOPUS:33645243360
SN - 0044-3255
VL - 98
SP - 414
EP - 424
JO - Parasitology Research
JF - Parasitology Research
IS - 5
ER -