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Bhat, U. S.

Publications and source records attributed to Bhat, U. S..

2 recordsLinked to original sources

FLP-15 modulates the amplitude of body bends during locomotion in Caenorhabditis elegans

Locomotion is essential for executing most behaviours. In Caenorhabditis elegans. Efficient locomotion is exhibited as a result of the coordination of excitatory and inhibitory signals from the nervous system onto the body-wall muscles. Although neurotransmitters play a vital role in maintaining and executing coordinated movements, neuropeptides have emerged as important players in the regulation and sustenance of locomotory states. In our previous study we explored the role of the neuropeptide FLP-15 in regulating reversal frequency during foraging behaviour in C. elegans. We were also interested in exploring other possible locomotory defects in flp-15 mutant animals. In this work we show that flp-15 mutants show an increased length of reversals during foraging resulting in defects in maintaining the direction of reversals. Mutants in flp-15 exhibited a "floral" pattern of reversals as opposed to near linear patterns of reversal in wild-type control animals. We further show that the defect in maintaining the direction of reversals could be due to increased amplitude of the body-bends with flp-15 mutants showing a large increase in the mean amplitude of body-bends. Our data suggests that FLP-15 partially functions through the G-protein coupled receptor (GPCR), NPR-3, to regulates the amplitude of body-bends. Finally, we show that loss of flp-15 leads to an increase in the expression of another neuropeptide, NLP-12, whose over expression has been implicated in causing increased amplitude of body-bends allowing us to speculate that the regulation of NLP-12 by FLP-15 may allow for the observed locomotory defects in flp-15 mutant animals.

neuroscience↗

FLP-15 functions through the GPCR NPR-3 to regulate local and global search behaviours in Caenorhabditis elegans

Foraging is essential for sustenance and well-being of all organisms. The transition from well-fed to food-deprived conditions in C. elegans triggers a localized exploration of the environment characterized by frequent reorientations. However, over time the cumulative frequency of these reorientations decreases, facilitating the transition to global search behaviour. To investigate the genetic regulation of foraging in C. elegans, we conducted a screen of neuropeptide mutants and identified several candidates involved in modulating this behaviour. Among these, neuropeptide FLP-15 emerged as a key regulator of both local and global search behaviours. Our observations revealed that FLP-15 regulates the frequency and duration of reversals during foraging. Further investigation indicated that FLP-15 is expressed in and functions through the I2 pharyngeal neuron via the G-protein coupled receptor NPR-3. Mutants lacking either flp-15 or npr-3 displayed a significant decrease in reversal frequency during local search behaviours. Interestingly, unlike wild-type animals, the reversal frequency in flp-15 and npr-3 mutants did not decrease over time. This study also describes the expression pattern of NPR-3, in a subset of head neurons, predominantly comprising of dopaminergic neurons. This expression pattern highlights a potential link between neuropeptide signalling and dopaminergic modulation of behaviour. Finally, exogenous dopamine supplementation assays revealed that FLP-15 may regulate foraging by modulating dopamine transmission, highlighting a novel neuropeptide-dopamine interaction involved in the control of foraging behaviours.

neuroscience↗