» Articles » PMID: 22081161

Nictation, a Dispersal Behavior of the Nematode Caenorhabditis Elegans, is Regulated by IL2 Neurons

Overview
Journal Nat Neurosci
Date 2011 Nov 15
PMID 22081161
Citations 94
Authors
Affiliations
Soon will be listed here.
Abstract

Many nematodes show a stage-specific behavior called nictation in which a worm stands on its tail and waves its head in three dimensions. Here we show that nictation is a dispersal behavior regulated by a specific set of neurons, the IL2 cells, in C. elegans. We established assays for nictation and showed that cholinergic transmission was required for nictation. Cell type-specific rescue experiments and genetic ablation experiments revealed that the IL2 ciliated head neurons were essential for nictation. Intact cilia in IL2 neurons, but not in other ciliated head neurons, were essential, as the restoration of the corresponding wild-type gene activity in IL2 neurons alone in cilia-defective mutants was sufficient to restore nictation. Optogenetic activation of IL2 neurons induced nictation, suggesting that signals from IL2 neurons are sufficient for nictation. Finally, we demonstrated that nictation is required for transmission of C. elegans to a new niche using flies as artificial carriers, suggesting a role of nictation as a dispersal and survival strategy under harsh conditions.

Citing Articles

The forkhead transcription factor FKH-7/FOXP acts in chemosensory neurons to regulate developmental decision-making.

Chai C, Taylor S, Tischbirek C, Wong W, Cai L, Miller D bioRxiv. 2025; .

PMID: 40027766 PMC: 11870486. DOI: 10.1101/2025.02.17.638733.


Carbon dioxide shapes parasite-host interactions in a human-infective nematode.

Banerjee N, Gang S, Castelletto M, Walsh B, Ruiz F, Hallem E Curr Biol. 2024; 35(2):277-286.e6.

PMID: 39719698 PMC: 11753939. DOI: 10.1016/j.cub.2024.11.036.


Life history in Caenorhabditis elegans: from molecular genetics to evolutionary ecology.

Braendle C, Paaby A Genetics. 2024; 228(3).

PMID: 39422376 PMC: 11538407. DOI: 10.1093/genetics/iyae151.


Glial expression of a steroidogenic enzyme underlies natural variation in hitchhiking behavior.

Yang H, Lee D, Kim H, Cook D, Paik Y, Andersen E Proc Natl Acad Sci U S A. 2024; 121(28):e2320796121.

PMID: 38959036 PMC: 11252821. DOI: 10.1073/pnas.2320796121.


Dendrite morphogenesis in Caenorhabditis elegans.

Heiman M, Bulow H Genetics. 2024; 227(2).

PMID: 38785371 PMC: 11151937. DOI: 10.1093/genetics/iyae056.


References
1.
Praitis V, Casey E, Collar D, Austin J . Creation of low-copy integrated transgenic lines in Caenorhabditis elegans. Genetics. 2001; 157(3):1217-26. PMC: 1461581. DOI: 10.1093/genetics/157.3.1217. View

2.
Jeong P, Jung M, Yim Y, Kim H, Park M, Hong E . Chemical structure and biological activity of the Caenorhabditis elegans dauer-inducing pheromone. Nature. 2005; 433(7025):541-5. DOI: 10.1038/nature03201. View

3.
Loer C, Kenyon C . Serotonin-deficient mutants and male mating behavior in the nematode Caenorhabditis elegans. J Neurosci. 1993; 13(12):5407-17. PMC: 6576401. View

4.
Hobert O . PCR fusion-based approach to create reporter gene constructs for expression analysis in transgenic C. elegans. Biotechniques. 2002; 32(4):728-30. DOI: 10.2144/02324bm01. View

5.
Mahoney T, Luo S, Nonet M . Analysis of synaptic transmission in Caenorhabditis elegans using an aldicarb-sensitivity assay. Nat Protoc. 2007; 1(4):1772-7. DOI: 10.1038/nprot.2006.281. View