The Importance of cGMP Signaling in Sensory Cilia for Body Size Regulation in Caenorhabditis elegans
Open accessAbstract
The body size of Caenorhabditis elegans is thought to be controlled by sensory inputs because many mutants with sensory cilium structure defects exhibit small body size. The EGL-4 cGMP-dependent protein kinase acts in sensory neurons to reduce body size when animals fail to perceive sensory signals. In addition to body size control, EGL-4 regulates various other behavioral and developmental pathways, including those involved in the regulation of egg laying and chemotaxis behavior. Here we have identified gcy-12, which encodes a receptor-type guanylyl cyclase, as a gene involved in the sensory regulation of body size. Analyses with GFP fusion constructs showed that gcy-12 is expressed in several sensory neurons and localizes to sensory cilia. Genetic analyses indicated that GCY-12 acts upstream of EGL-4 in body size control but does not affect other EGL-4 functions. Our studies indicate that the function of the GCY-12 guanylyl cyclase is to provide cGMP to the EGL-4 cGMP-dependent kinase only for limited tasks including body size regulation. We also found that the PDE-2 cyclic nucleotide phosphodiesterase negatively regulates EGL-4 in controlling body size. Thus, the cGMP level is precisely controlled by GCY-12 and PDE-2 to determine body size through EGL-4, and the defects in the sensory cilium structure may disturb the balanced control of the cGMP level. The large number of guanylyl cyclases encoded in the C. elegans genome suggests that EGL-4 exerts pleiotropic effects by partnering with different guanylyl cyclases for different downstream functions.
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C. elegans CFAP-20 participates in several sensory and physiological processes that depend on various types of non-motile cilia: gustatory plasticity, lifespan control, locomotion (roaming), and body size determination.
“Yet, C. elegans CFAP-20 participates in several sensory and physiological processes that depend on various types of non-motile cilia: ability to sense and learn to avoid salt in the absence of food (gustatory plasticity); lifespan control; locomotion (roaming); and, body size determination40,42,47–51.”
From The inner junction protein CFAP20 functions in motile and non-motile cilia and is critical for vision (2022) · cites this paper as [49]
Cites
THE GENETICS OF CAENORHABDITIS ELEGANS
Brenner, S. (1974) · Genetics · doi:10.1093/genetics/77.1.71 · Cited by 14,985 · see citing works
Mello, C. C., Kramer, J. M., Stinchcomb, D. T., & Ambros, V. (1991) · The EMBO Journal · doi:10.1002/j.1460-2075.1991.tb04966.x · Cited by 3,069 · see citing works
[C. elegans: of neurons and genes].
Gally, C., & Bessereau, J. (2003) · Medecine sciences : M/S · doi:10.1051/medsci/20031967725 · Cited by 2,194 · see citing works
Odorant-selective genes and neurons mediate olfaction in C. elegans
Bargmann, C. I., Hartwieg, E. A., & Horvitz, H. R. (1993) · Cell · doi:10.1016/0092-8674(93)80053-h · Cited by 1,211 · see citing works
Mutant sensory cilia in the nematode Caenorhabditis elegans
Perkins, L. A., Hedgecock, E. M., Thomson, J. N., & Culotti, J. G. (1986) · Developmental Biology · doi:10.1016/0012-1606(86)90314-3 · Cited by 907 · see citing works
Overview of PDEs and Their Regulation
Omori, K., & Kotera, J. (2007) · Circulation Research · doi:10.1161/01.res.0000256354.95791.f1 · Cited by 797 · see citing works
EGG-LAYING DEFECTIVE MUTANTS OF THE NEMATODE CAENORHABDITIS ELEGANS
Trent, C., Tsung, N., & Horvitz, H. R. (1983) · Genetics · doi:10.1093/genetics/104.4.619 · Cited by 729 · see citing works
Divergent seven transmembrane receptors are candidate chemosensory receptors in C. elegans
Troemel, E. R., Chou, J. H., Dwyer, N. D., Colbert, H. A., & Bargmann, C. I. (1995) · Cell · doi:10.1016/0092-8674(95)90162-0 · Cited by 684 · see citing works
Rapid gene mapping in Caenorhabditis elegans using a high density polymorphism map
Wicks, S. R., Yeh, R. T., Gish, W. R., Waterston, R., & Plasterk, R. H. A. (2001) · Nature Genetics · doi:10.1038/88878 · Cited by 649 · see citing works
Regulation of lifespan by sensory perception in Caenorhabditis elegans
Apfeld, J., & Kenyon, C. (1999) · Nature · doi:10.1038/45544 · Cited by 573 · see citing works
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 · see citing works
Komatsu, H., Mori, I., Rhee, J.-S., Akaike, N., & Ohshima, Y. (1996) · Neuron · doi:10.1016/s0896-6273(00)80202-0 · Cited by 446 · see citing works
Self-citationCoburn, C. M., & Bargmann, C. I. (1996) · Neuron · doi:10.1016/s0896-6273(00)80201-9 · Cited by 441 · see citing works
Guanylyl cyclase expression in specific sensory neurons: A new family of chemosensory receptors
Yu, S. S. B., Avery, L., Baude, E. J., & Garbers, D. L. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.7.3384 · Cited by 430 · see citing works
Regulation of Drosophila Life Span by Olfaction and Food-Derived Odors
Libert, S., Zwiener, J., Chu, X., VanVoorhies, W., Roman, G., & Pletcher, S. D. (2007) · Science · doi:10.1126/science.1136610 · Cited by 410 · see citing works
Control of Larval Development by Chemosensory Neurons in Caenorhabditis elegans
Bargmann, C. I., & Horvitz, H. R. (1991) · Science · doi:10.1126/science.2006412 · Cited by 405 · see citing works
Regulation of C. elegans Longevity by Specific Gustatory and Olfactory Neurons
Alcedo, J., & Kenyon, C. (2004) · Neuron · doi:10.1016/s0896-6273(03)00816-x · Cited by 388 · see citing works
High-Throughput In Vivo Analysis of Gene Expression in Caenorhabditis elegans
Hunt-Newbury, R., Viveiros, R., Johnsen, R. C., Mah, A. K., Anastas, D., Fang, L. L., Halfnight, E., Lee, D., Lin, J., Lorch, A. H., et al. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050237 · Cited by 372 · see citing works
Fujiwara, M., Sengupta, P., & McIntire, S. L. (2002) · Neuron · doi:10.1016/s0896-6273(02)01093-0 · Cited by 344 · see citing works
Self-citationBirnby, D., Link, E. M., Vowels, J. J., Tian, H., Colacurcio, P. L., & Thomas, J. H. (2000) · Genetics · doi:10.1093/genetics/155.1.85 · Cited by 328 · see citing works
Troemel, E. R., Sagasti, A., & Bargmann, C. I. (1999) · Cell · doi:10.1016/s0092-8674(00)81525-1 · Cited by 289 · see citing works
You, Y., Kim, J., Raizen, D. M., & Avery, L. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2008.01.005 · Cited by 269 · see citing works
Olfaction and Odor Discrimination Are Mediated by the C. elegans Guanylyl Cyclase ODR-1
L’Étoile, N. D., & Bargmann, C. I. (2000) · Neuron · doi:10.1016/s0896-6273(00)81061-2 · Cited by 264 · see citing works
Mutations affecting the chemosensory neurons of Caenorhabditis elegans.
Starich, T. A., Herman, R. K., Kari, C. K., Yeh, W. H., Schackwitz, W., Schuyler, M. W., Collet, J., Thomas, J. H., & Riddle, D. L. (1995) · Genetics · doi:10.1093/genetics/139.1.171 · Cited by 262 · see citing works
Gengyo‐Ando, K., & Mitani, S. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.2260 · Cited by 213 · see citing works
The Cyclic GMP-Dependent Protein Kinase EGL-4 Regulates Olfactory Adaptation in C. elegans
L’Étoile, N. D., Coburn, C. M., Eastham, J., Kistler, A. L., Gallegos, G., & Bargmann, C. I. (2002) · Neuron · doi:10.1016/s0896-6273(02)01066-8 · Cited by 202 · see citing works
Polygenic control of Caenorhabditis elegans fat storage
Mak, H. Y., Nelson, L. S., Basson, M., Johnson, C. D., & Ruvkun, G. (2006) · Nature Genetics · doi:10.1038/ng1739 · Cited by 194 · see citing works
Specific neuroanatomical changes in chemosensory mutants of the nematode Caenorhabditis elegans
Lewis, J. A., & Hodgkin, J. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901720306 · Cited by 191 · see citing works
Identification of Guanylyl Cyclases That Function in Thermosensory Neurons of Caenorhabditis elegans
Inada, H., Itô, H., Satterlee, J. S., Sengupta, P., Matsumoto, K., & Mori, I. (2006) · Genetics · doi:10.1534/genetics.105.050013 · Cited by 178 · see citing works
Self-citationIntraflagellar transport and the generation of dynamic, structurally and functionally diverse cilia
Silverman, M. A., & Leroux, M. R. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2009.04.002 · Cited by 161 · see citing works
Negative Regulation and Gain Control of Sensory Neurons by the C. elegans Calcineurin TAX-6
Kuhara, A., Inada, H., Katsura, I., & Mori, I. (2002) · Neuron · doi:10.1016/s0896-6273(02)00607-4 · Cited by 153 · see citing works
Self-citationOrtiz, C. O., Etchberger, J. F., Posy, S., Frøkjær‐Jensen, C., Lockery, S. R., Honig, B. H., & Hobert, O. (2006) · Genetics · doi:10.1534/genetics.106.055749 · Cited by 133 · see citing works
Receptor-type guanylate cyclase is required for carbon dioxide sensation by Caenorhabditis elegans
Hallem, E. A., Spencer, W. C., McWhirter, R. D., Zeller, G., Henz, S. R., Rätsch, G., Miller, D. M., Horvitz, H. R., Sternberg, P. W., & Ringstad, N. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1017354108 · Cited by 131 · see citing works
Ortiz, C. O., Faumont, S., Takayama, J., Ahmed, H. K., Goldsmith, A. D., Pocock, R., McCormick, K. E., Kunimoto, H., Iino, Y., Lockery, S. R., et al. (2009) · Current Biology · doi:10.1016/j.cub.2009.05.043 · Cited by 113 · see citing works
Daniels, S. A., Ailion, M., Thomas, J. H., & Sengupta, P. (2000) · Genetics · doi:10.1093/genetics/156.1.123 · Cited by 105 · see citing works
A novel WD40 protein, CHE-2, acts cell-autonomously in the formation of C. elegans sensory cilia
Fujiwara, M., Ishihara, T., & Katsura, I. (1999) · Development · doi:10.1242/dev.126.21.4839 · Cited by 103 · see citing works
Self-citationCyclic GMP-dependent protein kinase EGL-4 controls body size and lifespan inC. elegans
Hirose, T., Nakano, Y., Nagamatsu, Y., Misumi, T., Ohta, H., & Ohshima, Y. (2003) · Development · doi:10.1242/dev.00330 · Cited by 101 · see citing works
Self-citationEndogenous Nuclear RNAi Mediates Behavioral Adaptation to Odor
Juang, B.-T., Gu, C., Starnes, L. M., Palladino, F., Goga, A., Kennedy, S. G., & L’Étoile, N. D. (2013) · Cell · doi:10.1016/j.cell.2013.08.006 · Cited by 89 · see citing works
Regulation of Chemosensory Receptor Expression and Sensory Signaling by the KIN-29 Ser/Thr Kinase
Lanjuin, A., & Sengupta, P. (2002) · Neuron · doi:10.1016/s0896-6273(02)00572-x · Cited by 71 · see citing works
Invertebrates Yield a Plethora of Atypical Guanylyl Cyclases
Morton, D. B. (2004) · Molecular Neurobiology · doi:10.1385/mn:29:2:097 · Cited by 63 · see citing works
Wang, D., O’Halloran, D. M., & Goodman, M. B. (2013) · The Journal of General Physiology · doi:10.1085/jgp.201310959 · Cited by 62 · see citing works
Raizen, D. M., Cullison, K., Pack, A. I., & Sundaram, M. V. (2006) · Genetics · doi:10.1534/genetics.106.057380 · Cited by 62 · see citing works
Charlie, N. K., Thomure, A. M., Schade, M. A., & Miller, K. G. (2006) · Genetics · doi:10.1534/genetics.105.054007 · Cited by 53 · see citing works
van der Linden, A. M., Wiener, S. M., You, Y., Kim, K., Avery, L., & Sengupta, P. (2008) · Genetics · doi:10.1534/genetics.108.094771 · Cited by 45 · see citing works
Hao, Y., Xu, N., Box, A., Schaefer, L., Kannan, K. S., Zhang, Y., Florens, L. A., Seidel, C. W., Washburn, M. P., Wiegraebe, W., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002065 · Cited by 42 · see citing works
In vivo genetic dissection of O 2 -evoked cGMP dynamics in a Caenorhabditis elegans gas sensor
Couto, A., Oda, S., Nikolaev, V. O., Soltész, Z., & de Bono, M. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1217428110 · Cited by 41 · see citing works
Dietary regulation of hypodermal polyploidization in C. elegans
Tain, L. S., Lozano, E., Sáez, A. G., & Leroi, A. M. (2008) · BMC Developmental Biology · doi:10.1186/1471-213x-8-28 · Cited by 39 · see citing works
Changes in cGMP Levels Affect the Localization of EGL-4 in AWC in Caenorhabditis elegans
O’Halloran, D. M., Hamilton, O. S., Lee, J. I., Gallegos, M. E., & L’Étoile, N. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031614 · Cited by 38 · see citing works
A cGMP‐dependent protein kinase is implicated in wild‐type motility in C. elegans
Stansberry, J., Baude, E. J., Taylor, M. K., Chen, P., Jin, S., Ellis, R. E., & Uhler, M. D. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00131.x · Cited by 33 · see citing works
Environmental Alkalinity Sensing Mediated by the Transmembrane Guanylyl Cyclase GCY-14 in C. elegans
Murayama, T., Takayama, J., Fujiwara, M., & MARUYAMA, I. N. (2013) · Current Biology · doi:10.1016/j.cub.2013.04.052 · Cited by 31 · see citing works
Self-citationFujiwara, M., Teramoto, T., Ishihara, T., Ohshima, Y., & McIntire, S. L. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001211 · Cited by 25 · see citing works
Self-citationGross, E., Soltész, Z., Oda, S., Zelmanovich, V., Abergel, Z., & de Bono, M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.5368-13.2014 · Cited by 22 · see citing works
Nakano, Y., Nagamatsu, Y., & Ohshima, Y. (2004) · Genes to Cells · doi:10.1111/j.1365-2443.2004.00771.x · Cited by 19 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Chemosensory signal transduction in Caenorhabditis elegans
Ferkey, D. M., Sengupta, P., & L’Étoile, N. D. (2021) · Genetics · doi:10.1093/genetics/iyab004 · Cited by 133 · see citing works
PDE inhibition in distinct cell types to reclaim the balance of synaptic plasticity
Rombaut, B., Kessels, S., Schepers, M., Tiane, A., Paes, D., Solomina, Y., Piccart, E., van den Hove, D., Brône, B., Prickaerts, J., et al. (2020) · Theranostics · doi:10.7150/thno.50701 · Cited by 32 · see citing works
Chrystal, P. W., Lambacher, N. J., Doucette, L. P., Bellingham, J., Schiff, E. R., Noel, N. C. L., Li, C., Tsiropoulou, S., Casey, G. A., Zhai, Y., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-33820-w · Cited by 31 · see citing works
Ravi, B., Zhao, J., Chaudhry, S. I., Signorelli, R., Bartole, M. K., Kopchock, R. J., Guijarro, C., Kaplan, J. M., Kang, L., & Collins, K. M. (2021) · Genetics · doi:10.1093/genetics/iyab080 · Cited by 25 · see citing works
Receptor Guanylyl Cyclases in Sensory Processing
MARUYAMA, I. N. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2016.00173 · Cited by 24 · see citing works
ROS and cGMP signaling modulate persistent escape from hypoxia in Caenorhabditis elegans
Zhao, L., Fenk, L. A., Nilsson, L., Amin-Wetzel, N., Ramírez-Suárez, N. J., de Bono, M., & Chen, C. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001684 · Cited by 23 · see citing works
Control of Neuropeptide Expression by Parallel Activity-dependent Pathways in Caenorhabditis elegans
Romanos, T. R., Petersen, J. G., & Pocock, R. (2017) · Scientific Reports · doi:10.1038/srep38734 · Cited by 22 · see citing works
Active propagation of dendritic electrical signals in C. elegans
Shindou, T., Ochi-Shindou, M., Murayama, T., Saita, E., Momohara, Y., Wickens, J. R., & MARUYAMA, I. N. (2019) · Scientific Reports · doi:10.1038/s41598-019-40158-9 · Cited by 22 · see citing works
Pimentel-Acosta, C. A., Ramírez-Salcedo, J., Morales-Serna, F. N., Fajer-Avila, E. J., Chávez‐Sánchez, M. C., Lara, H. H., & Garcı́a-Gasca, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21165889 · Cited by 18 · see citing works
Selection and the direction of phenotypic evolution
Mallard, F., Afonso, B., & Teotónio, H. (2023) · eLife · doi:10.7554/elife.80993 · Cited by 17 · see citing works
Wu, J., Yin, S.-W., Liu, H., Li, R., Huang, J.-H., Wang, P.-Z., Xu, Y., Zhao, J.-L., Wu, P.-P., & Wu, Z. (2022) · iScience · doi:10.1016/j.isci.2022.105287 · Cited by 14 · see citing works
Liu, W., Shao, H., Qi, D., Huang, X., Chen, J., Zhou, L., & Guo, K. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25136914 · Cited by 12 · see citing works
Boanerges Aleman-meza, A., Cabrera, M. L., Peña-Ramos, O., Stern, M., & Zhong, W. (2017) · BMC Genetics · doi:10.1186/s12863-017-0513-7 · Cited by 8 · see citing works
Liu, Y., Wang, R. J., Ru, S. S., Gao, F., Liu, W. Y., & Zhang, X. (2024) · Parasites & Vectors · doi:10.1186/s13071-024-06454-8 · Cited by 6 · see citing works
Xu, Y., Chen, L., Liu, M., Lu, Y., Yue, Y., Liu, Y., Chen, H., Xie, F., & Zhang, C. (2019) · Toxicology Research · doi:10.1039/c9tx00101h · Cited by 4 · see citing works
Galande, K. K., & Cote, R. (2025) · Cells · doi:10.3390/cells14151174 · Cited by 2 · see citing works
Pandey, A., Katz, M., Nurrish, S., Philbrook, A., & Sengupta, P. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2519437123 · Cited by 2 · see citing works
Ravi, B., Zhao, J., Chaudhry, S. I., Bartole, M. K., Kopchock, R. J., Guijarro, C., Kang, L., & Collins, K. M. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/701664 · Cited by 2 · see citing works
Pandey, A., Katz, M., Nurrish, S., Philbrook, A., & Sengupta, P. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.25.666858 · Cited by 2 · see citing works
Membrane-Bound Guanylyl Cyclases within the Ciliary Compartment
He, Y., & Pan, J. (2025) · Biochemistry · doi:10.1021/acs.biochem.5c00326 · Cited by 1 · see citing works
Chen, X., Shi, Y., Wang, T., Liu, C., Wang, W., & Wang, Y. (2025) · Frontiers in Veterinary Science · doi:10.3389/fvets.2025.1567869 · Cited by 1 · see citing works
Cilium length regulation in Caenorhabditis elegans
Park, K. (2019) · Summit (Simon Fraser University)
Liu, Y., Wang, R. J., Ru, S. S., Gao, F., Liu, W., & Zhang, X. (2024) · Figshare · doi:10.6084/m9.figshare.26944671
Liu, Y., Wang, R. J., Ru, S. S., Gao, F., Liu, W., & Zhang, X. (2024) · Figshare · doi:10.6084/m9.figshare.26944668
Liu, Y. Y., Wang, R. J., Ru, S. S., Gao, F., Liu, W., & Zhang, X. (2024) · Figshare · doi:10.6084/m9.figshare.26944659
Liu, Y. Y., Wang, R. J., Ru, S. S., Gao, F., Liu, W., & Zhang, X. (2024) · Figshare · doi:10.6084/m9.figshare.26944665
Liu, Y., Wang, R. J., Ru, S. S., Gao, F., Liu, W., & Zhang, X. (2024) · Figshare · doi:10.6084/m9.figshare.26944662
- Authors
- Fujiwara, M., Hino, T., Miyamoto, R., Inada, H., Mori, I., Koga, M., Miyahara, K., Ohshima, Y., & Ishihara, T.
- Affiliations
- Kyushu University (JP)
- Tohoku University (JP)
- Nagoya University (JP)
- Sojo University (JP)
- Corresponding author
- Fujiwara, Manabi
- Venue
- Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2015-10-04
- Volume
- 201
- Issue
- 4
- Pages
- 1497-1510
- ISSN
- 0016-6731 (ISSN-L)
- 1943-2631
- PMC
- PMC4676540
- OpenAlex
- W2177301250
- Cited by
- 23
- References
- 53
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 3 · 2023: 1 · 2022: 3 · 2021: 2 · 2020: 2 · 2019: 4 · 2017: 3
- FWCI
- 0.68
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- Genetics (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Society for the Promotion of Science (221S0003, 15K14574, 24247001, 25115009)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Kidney Cyst Diseases
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Phosphodiesterase function and regulation
- Keywords
- body size regulation, sensory cilia, cGMP signaling, egl-4, cyclic nucleotide phosphodiesterase, sensory neurons, Caenorhabditis elegans, sensory perception, chemotaxis, oviposition
- MeSH terms
- Animals, Cilia, Cyclic GMP, Sensory Receptor Cells, Suppression, Genetic, Signal Transduction, Caenorhabditis elegans, Genes, Helminth, Caenorhabditis elegans Proteins, Body Size
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