The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Functional Genomic Analysis of C. elegans Molting
Open accessAbstract
Although the molting cycle is a hallmark of insects and nematodes, neither the endocrine control of molting via size, stage, and nutritional inputs nor the enzymatic mechanism for synthesis and release of the exoskeleton is well understood. Here, we identify endocrine and enzymatic regulators of molting in C. elegans through a genome-wide RNA-interference screen. Products of the 159 genes discovered include annotated transcription factors, secreted peptides, transmembrane proteins, and extracellular matrix enzymes essential for molting. Fusions between several genes and green fluorescent protein show a pulse of expression before each molt in epithelial cells that synthesize the exoskeleton, indicating that the corresponding proteins are made in the correct time and place to regulate molting. We show further that inactivation of particular genes abrogates expression of the green fluorescent protein reporter genes, revealing regulatory networks that might couple the expression of genes essential for molting to endocrine cues. Many molting genes are conserved in parasitic nematodes responsible for human disease, and thus represent attractive targets for pesticide and pharmaceutical development.
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Cites
Evidence for a clade of nematodes, arthropods and other moulting animals
Aguinaldo, A. M. A., Turbeville, J. M., Linford, L. S., Rivera, M. C., Garey, J. R., Raff, R. A., & Lake, J. A. (1997) · Nature · doi:10.1038/387489a0 · Cited by 1,609
DAF-16 Target Genes That Control C. elegans Life-Span and Metabolism
Lee, S. S., Kennedy, S., Tolonen, A. C., & Ruvkun, G. (2003) · Science · doi:10.1126/science.1083614 · Cited by 669
Self-citationControl and biochemical nature of the ecdysteroidogenic pathway
Gilbert, L. I., Rybczynski, R., & Warren, J. T. (2002) · Annual Review of Entomology · doi:10.1146/annurev.ento.47.091201.145302 · Cited by 532 · cited 3×
“Production of a ligand for NHR-23 is likely to be tightly regulated, similar to how steroidogenesis in the prothoracic gland of insects is induced by the neuropeptide prothoracicotropic hormone but also repressed by ecdysteroids [3,70].”
BackgroundEdens, W. A., Sharling, L., Cheng, G., Shapira, R., Kinkade, J. M., Lee, T., Edens, H. A., Tang, X., Sullards, C., Flaherty, D. B., et al. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.200103132 · Cited by 375
Cited by
Cao, J., Packer, J. S., Ramani, V., Cusanovich, D. A., Huynh, C., Daza, R., Qiu, X., Lee, C., Furlan, S. N., Steemers, F. J., et al. (2017) · doi:10.1101/104844 · Cited by 1,402
Lethargus is a Caenorhabditis elegans sleep-like state
Raizen, D. M., Zimmerman, J. E., Maycock, M. H., Ta, U. D., You, Y.-J., Sundaram, M. V., & Pack, A. I. (2008) · Nature · doi:10.1038/nature06535 · Cited by 536
Enzymes for ecdysteroid biosynthesis: Their biological functions in insects and beyond
Niwa, R., & Niwa, Y. S. (2014) · Bioscience, Biotechnology, and Biochemistry · doi:10.1080/09168451.2014.942250 · Cited by 249
Trojanowski, N. F., & Raizen, D. M. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2015.12.005 · Cited by 132
Brenner, J. L., Jasiewicz, K. L., Fahley, A. F., Kemp, B. J., & Abbott, A. L. (2010) · Current Biology · doi:10.1016/j.cub.2010.05.062 · Cited by 123
Metadata
- Authors
- Frand, A. R., Russel, S., & Ruvkun, G.
- Venue
- PLoS Biology
- Publisher
- Public Library of Science (PLoS)
- Published
- 2005-08-30
- Volume
- 3
- Issue
- 10
- Pages
- e312
- ISSN
- 1544-9173 (ISSN-L)
- 1545-7885
- OpenAlex
- W2147515706
- Cited by
- 296
- References
- 4
- FWCI
- 4.53
- Type
- journal article
- Language
- en
- Open access
- gold
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