The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
The Parasitome of the Phytonematode Heterodera glycines
Abstract
Parasitism genes expressed in the esophageal gland cells of phytonematodes encode secretions that control the complex process of plant parasitism. In the soybean cyst nematode, Heterodera glycines, the parasitome, i.e., the secreted products of parasitism genes, facilitate nematode migration in soybean roots and mediate the modification of root cells into elaborate feeding cells required to support the growth and development of the nematode. With very few exceptions, the identities of these secretions are unknown, and the mechanisms of cyst nematode parasitism, therefore, remain obscure. The most direct and efficient approach for cloning parasitism genes and rapidly advancing our understanding of the molecular interactions during nematode parasitism of plants is to create gland cell-specific cDNA libraries using cytoplasm microaspirated from the esophageal gland cells of various parasitic stages. By combining expressed sequence tag analysis of a gland cell cDNA library with high throughput in situ expression localization of clones encoding secretory proteins, we obtained the first comprehensive parasitome profile for a parasitic nematode. We identified 51 new H. glycines gland-expressed candidate parasitism genes, of which 38 genes constitute completely novel sequences. Individual parasitome members showed distinct gland cell expression patterns throughout the parasitic cycle. The parasitome complexity discovered paints a more elaborate picture of host cellular events under specific control by the nematode parasite than previously hypothesized.
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Cites
Base-Calling of Automated Sequencer Traces Using Phred. II. Error Probabilities
Ewing, B., & Green, P. (1998) · Genome Research · doi:10.1101/gr.8.3.186 · Cited by 5,439
Nakai, K., & Horton, P. (1999) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(98)01336-x · Cited by 2,181 · cited 1×
“Transmembrane regions and subcellular localization sites of the deduced proteins were predicted by TMHMM (Krogh et al. 2001) and PSORT II (Nakai and Horton 1999), respectively.”
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Cited by
Top 10 plant‐parasitic nematodes in molecular plant pathology
Jones, J. T., Haegeman, A., Danchin, E. G. J., Gaur, H. S., Helder, J., Jones, M. G. K., Kikuchi, T., Manzanilla‐López, R., Palomares‐Rius, J. E., Wesemael, W. M. L., et al. (2013) · Molecular Plant Pathology · doi:10.1111/mpp.12057 · Cited by 2,315
Ubiquitin, Hormones and Biotic Stress in Plants
Dreher, K., & Callis, J. (2007) · Annals of Botany · doi:10.1093/aob/mcl255 · Cited by 503
Kikuchi, T., Cotton, J. A., Dalzell, J. J., Hasegawa, K., Kanzaki, N., McVeigh, P., Takanashi, T., Tsai, I. J., Assefa, S. A., Cock, P. J. A., et al. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002219 · Cited by 428
Nematode effector proteins: an emerging paradigm of parasitism
Mitchum, M. G., Hussey, R. S., Baum, T. J., Wang, X., Elling, A. A., Wubben, M., & Davis, E. L. (2013) · New Phytologist · doi:10.1111/nph.12323 · Cited by 355
Self-citationGetting to the roots of parasitism by nematodes
Davis, E. (2004) · Trends in Parasitology · doi:10.1016/j.pt.2004.01.005 · Cited by 309
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Metadata
- Authors
- Gao, B., Allen, R., Maier, T., Davis, E. L., Baum, T. J., & Hussey, R. S.
- Venue
- Molecular Plant-Microbe Interactions®
- Publisher
- Scientific Societies
- Published
- 2003-08
- Volume
- 16
- Issue
- 8
- Pages
- 720-726
- ISSN
- 0894-0282 (ISSN-L)
- 1943-7706
- OpenAlex
- W2170738491
- Cited by
- 282
- References
- 2
- FWCI
- 9.94
- Type
- journal article
- Language
- en
- Open access
- closed
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