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CNP-1 (ARRD-17), a Novel Substrate of Calcineurin, Is Critical for Modulation of Egg-Laying and Locomotion in Response to Food and Lysine Sensation in Caenorhabditis elegans

Authors
Jee, ChanghoonChoi, Tae-WooKalichamy, KarunambigaiYee, Jong ZinSong, Hyun-OkJi, Yon JuLee, JungsooLee, Jin IlL'Etoile, Noelle D.Ahnn, JoohongLee, Sun-Kyung
Issue Date
Mar-2012
Publisher
ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
Keywords
calcineurin; CNP-1; ARRD-17; ASK; ASH
Citation
JOURNAL OF MOLECULAR BIOLOGY, v.417, no.3, pp.165 - 178
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF MOLECULAR BIOLOGY
Volume
417
Number
3
Start Page
165
End Page
178
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/166174
DOI
10.1016/j.jmb.2012.01.012
ISSN
0022-2836
Abstract
Calcineurin is a Ca2+/calmodulin-dependent protein phosphatase involved in calcium signaling pathways. In Caenorhabditis elegans, the loss of calcineurin activity causes pleiotropic defects including hyperadaptation of sensory neurons, hypersensation to thermal difference and hyper-egg-laying when worms are refed after starvation. In this study, we report on arrd-17 as calcineurin-interacting protein-1 (cnp-1), which is a novel molecular target of calcineurin. CNP-1 interacts with the catalytic domain of the C. elegans calcineurin A subunit, TAX-6, in a yeast two-hybrid assay and is dephosphorylated by TAX-6 in vitro. cnp-1 is expressed in ASK, ADL, ASH and ASJ sensory neurons as TAX-6. It acts downstream of tax-6 in regulation of locomotion and egg-laying after starvation, ASH sensory neuron adaptation and lysine chemotaxis, that is known to be mediated by ASK neurons. Altogether, our biochemical and genetic evidence indicates that CNP-1 is a direct target of calcineurin and required in stimulated egg-laying and locomotion after starvation, adaptation to hyperosmolarity and attraction to lysine, which is modulated by calcineurin. We suggest that the phosphorylation status of CNP-1 plays an important role in regulation of refed stimulating behaviors after starvation and attraction to amino acid, which provides valuable nutritious information.
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