Abstract
Dauer larva formation in Caenorhabditis elegans is controlled by chemosensory cells that respond to environmental cues. Genetic interactions among mutations in 23 genes that affect dauer larva formation were investigated. Mutations in seven genes that cause constitutive dauer formation, and mutations in 16 genes that either block dauer formation or result in the formation of abnormal dauers, were analyzed. Double mutants between dauer-constitutive and dauer-defective mutations were constructed and characterized for their capacity to form dauer larvae. Many of the genes could be interpreted to lie in a simple linear epistasis pathway. Three genes, daf-16, daf-18 and daf-20, may affect downstream steps in a branched part of the pathway. Three other genes, daf-2, daf-3 and daf-5, displayed partial or complex epistasis interactions that were difficult to interpret as part of a simple linear pathway. Dauer-defective mutations in nine genes cause structurally defective chemosensory cilia, thereby blocking chemosensation. Mutations in all nine of these genes appear to fall at a single step in the epistasis pathway. Dauer-constitutive mutations in one gene, daf-11, were strongly suppressed for dauer formation by mutations in the nine cilium-structure genes. Mutations in the other six dauer-constitutive genes caused dauer formation despite the absence of functional chemosensory endings. These results suggest that daf-11 is directly involved in chemosensory transduction essential for dauer formation, while the other Daf-c genes play roles downstream of the chemosensory step.
Full Text
The Full Text of this article is available as a PDF (4.5 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Albert P. S., Brown S. J., Riddle D. L. Sensory control of dauer larva formation in Caenorhabditis elegans. J Comp Neurol. 1981 May 20;198(3):435–451. doi: 10.1002/cne.901980305. [DOI] [PubMed] [Google Scholar]
- Albert P. S., Riddle D. L. Mutants of Caenorhabditis elegans that form dauer-like larvae. Dev Biol. 1988 Apr;126(2):270–293. doi: 10.1016/0012-1606(88)90138-8. [DOI] [PubMed] [Google Scholar]
- Bargmann C. I., Horvitz H. R. Control of larval development by chemosensory neurons in Caenorhabditis elegans. Science. 1991 Mar 8;251(4998):1243–1246. doi: 10.1126/science.2006412. [DOI] [PubMed] [Google Scholar]
- Cassada R. C., Russell R. L. The dauerlarva, a post-embryonic developmental variant of the nematode Caenorhabditis elegans. Dev Biol. 1975 Oct;46(2):326–342. doi: 10.1016/0012-1606(75)90109-8. [DOI] [PubMed] [Google Scholar]
- Culotti J. G., Russell R. L. Osmotic avoidance defective mutants of the nematode Caenorhabditis elegans. Genetics. 1978 Oct;90(2):243–256. doi: 10.1093/genetics/90.2.243. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Golden J. W., Riddle D. L. A gene affecting production of the Caenorhabditis elegans dauer-inducing pheromone. Mol Gen Genet. 1985;198(3):534–536. doi: 10.1007/BF00332953. [DOI] [PubMed] [Google Scholar]
- Golden J. W., Riddle D. L. A pheromone influences larval development in the nematode Caenorhabditis elegans. Science. 1982 Nov 5;218(4572):578–580. doi: 10.1126/science.6896933. [DOI] [PubMed] [Google Scholar]
- Golden J. W., Riddle D. L. A pheromone-induced developmental switch in Caenorhabditis elegans: Temperature-sensitive mutants reveal a wild-type temperature-dependent process. Proc Natl Acad Sci U S A. 1984 Feb;81(3):819–823. doi: 10.1073/pnas.81.3.819. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hedgecock E. M., Culotti J. G., Thomson J. N., Perkins L. A. Axonal guidance mutants of Caenorhabditis elegans identified by filling sensory neurons with fluorescein dyes. Dev Biol. 1985 Sep;111(1):158–170. doi: 10.1016/0012-1606(85)90443-9. [DOI] [PubMed] [Google Scholar]
- Hereford L. M., Hartwell L. H. Sequential gene function in the initiation of Saccharomyces cerevisiae DNA synthesis. J Mol Biol. 1974 Apr 15;84(3):445–461. doi: 10.1016/0022-2836(74)90451-3. [DOI] [PubMed] [Google Scholar]
- Herman R. K. Analysis of genetic mosaics of the nematode Caneorhabditis elegans. Genetics. 1984 Sep;108(1):165–180. doi: 10.1093/genetics/108.1.165. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Horvitz H. R., Brenner S., Hodgkin J., Herman R. K. A uniform genetic nomenclature for the nematode Caenorhabditis elegans. Mol Gen Genet. 1979 Sep;175(2):129–133. doi: 10.1007/BF00425528. [DOI] [PubMed] [Google Scholar]
- Perkins L. A., Hedgecock E. M., Thomson J. N., Culotti J. G. Mutant sensory cilia in the nematode Caenorhabditis elegans. Dev Biol. 1986 Oct;117(2):456–487. doi: 10.1016/0012-1606(86)90314-3. [DOI] [PubMed] [Google Scholar]
- Sulston J. E., Albertson D. G., Thomson J. N. The Caenorhabditis elegans male: postembryonic development of nongonadal structures. Dev Biol. 1980 Aug;78(2):542–576. doi: 10.1016/0012-1606(80)90352-8. [DOI] [PubMed] [Google Scholar]
- Trent C., Tsuing N., Horvitz H. R. Egg-laying defective mutants of the nematode Caenorhabditis elegans. Genetics. 1983 Aug;104(4):619–647. doi: 10.1093/genetics/104.4.619. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ward S., Thomson N., White J. G., Brenner S. Electron microscopical reconstruction of the anterior sensory anatomy of the nematode Caenorhabditis elegans.?2UU. J Comp Neurol. 1975 Apr 1;160(3):313–337. doi: 10.1002/cne.901600305. [DOI] [PubMed] [Google Scholar]
- Wu XG, Dev G, Jain JK. Mixed-spin incompressible states in the fractional quantum Hall effect. Phys Rev Lett. 1993 Jul 5;71(1):153–156. doi: 10.1103/PhysRevLett.71.153. [DOI] [PubMed] [Google Scholar]