Gene/Protein
Disease
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Enzyme
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Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
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Target Concepts:
Gene/Protein
Disease
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Drug
Enzyme
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Query: EC:2.7.11.17 (
CaMKII
)
4,029
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The ability to adapt behavior to environmental fluctuations is critical for survival of organisms ranging from invertebrates to mammals.
Caenorhabditis elegans
can learn to avoid sodium chloride when it is paired with starvation. This behavior may help animals avoid areas without food. Although some genes have been implicated in this
salt
-aversive learning behavior, critical genetic components, and the neural circuit in which they act, remain elusive. Here, we show that the sole worm ortholog of mammalian
CaMKI
/IV, CMK-1, is essential for
salt
-aversive learning behavior in
C. elegans
hermaphrodites. We find that CMK-1 acts in the primary
salt
-sensing ASE neurons to regulate this behavior. By characterizing the intracellular calcium dynamics in ASE neurons using microfluidics, we find that loss of
cmk-1
has subtle effects on sensory-evoked calcium responses in ASE axons and their modulation by
salt
conditioning. Our study implicates the expression of the conserved
CaMKI
/CMK-1 in chemosensory neurons as a regulator of behavioral plasticity to environmental
salt
in
C. elegans
SIGNIFICANCE STATEMENT
Like other animals, the nematode
Caenorhabditis elegans
depends on
salt
for survival and navigates toward high concentrations of this essential mineral. In addition to its role as an essential nutrient,
salt
also causes osmotic stress at high concentrations. A growing body of evidence indicates that
C. elegans
balances the requirement for
salt
with the danger it presents through a process called
salt
-aversive learning. We show that this behavior depends on expression of a calcium/calmodulin-dependent kinase, CMK-1, in the ASE
salt
-sensing neurons. Our study identifies CMK-1 and
salt
-sensitive chemosensory neurons as key factors in this form of behavioral plasticity.
...
PMID:Loss of CaMKI Function Disrupts Salt Aversive Learning in
C. elegans
. 2987 64
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