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Developmental genetics of the C. elegans pharyngeal neurons NSML and NSMR

BACKGROUND: We are interested in understanding how the twenty neurons of the C. elegans pharynx develop in an intricate yet reproducible way within the narrow confines of the embryonic pharyngeal primordium. To complement an earlier study of the pharyngeal M2 motorneurons, we have now examined the e...

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Autores principales: Axäng, Claes, Rauthan, Manish, Hall, David H, Pilon, Marc
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375884/
https://www.ncbi.nlm.nih.gov/pubmed/18400083
http://dx.doi.org/10.1186/1471-213X-8-38
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author Axäng, Claes
Rauthan, Manish
Hall, David H
Pilon, Marc
author_facet Axäng, Claes
Rauthan, Manish
Hall, David H
Pilon, Marc
author_sort Axäng, Claes
collection PubMed
description BACKGROUND: We are interested in understanding how the twenty neurons of the C. elegans pharynx develop in an intricate yet reproducible way within the narrow confines of the embryonic pharyngeal primordium. To complement an earlier study of the pharyngeal M2 motorneurons, we have now examined the effect of almost forty mutations on the morphology of a bilateral pair of pharyngeal neurosecretory-motor neurons, the NSMs. RESULTS: A careful description of the NSM morphology led to the discovery of a third, hitherto unreported process originating from the NSM cell body and that is likely to play a proprioceptive function. We found that the three NSM processes are differently sensitive to mutations. The major dorsal branch was most sensitive to mutations that affect growth cone guidance and function (e.g. unc-6, unc-34, unc-73), while the major sub-ventral branch was more sensitive to mutations that affect components of the extracellular matrix (e.g. sdn-1). Of the tested mutations, only unc-101, which affects an adaptin, caused the loss of the newly described thin minor process. The major processes developed synaptic branches post-embryonically, and these exhibited activity-dependent plasticity. CONCLUSION: By studying the effects of nearly forty different mutations we have learned that the different NSM processes require different genes for their proper guidance and use both growth cone dependent and growth cone independent mechanisms for establishing their proper trajectories. The two major NSM processes develop in a growth cone dependent manner, although the sub-ventral process relies more on substrate adhesion. The minor process also uses growth cones but uniquely develops using a mechanism that depends on the clathrin adaptor molecule UNC-101. Together with the guidance of the M2 neuron, this is the second case of a pharyngeal neuron establishing one of its processes using an unexpected mechanism.
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spelling pubmed-23758842008-05-10 Developmental genetics of the C. elegans pharyngeal neurons NSML and NSMR Axäng, Claes Rauthan, Manish Hall, David H Pilon, Marc BMC Dev Biol Research Article BACKGROUND: We are interested in understanding how the twenty neurons of the C. elegans pharynx develop in an intricate yet reproducible way within the narrow confines of the embryonic pharyngeal primordium. To complement an earlier study of the pharyngeal M2 motorneurons, we have now examined the effect of almost forty mutations on the morphology of a bilateral pair of pharyngeal neurosecretory-motor neurons, the NSMs. RESULTS: A careful description of the NSM morphology led to the discovery of a third, hitherto unreported process originating from the NSM cell body and that is likely to play a proprioceptive function. We found that the three NSM processes are differently sensitive to mutations. The major dorsal branch was most sensitive to mutations that affect growth cone guidance and function (e.g. unc-6, unc-34, unc-73), while the major sub-ventral branch was more sensitive to mutations that affect components of the extracellular matrix (e.g. sdn-1). Of the tested mutations, only unc-101, which affects an adaptin, caused the loss of the newly described thin minor process. The major processes developed synaptic branches post-embryonically, and these exhibited activity-dependent plasticity. CONCLUSION: By studying the effects of nearly forty different mutations we have learned that the different NSM processes require different genes for their proper guidance and use both growth cone dependent and growth cone independent mechanisms for establishing their proper trajectories. The two major NSM processes develop in a growth cone dependent manner, although the sub-ventral process relies more on substrate adhesion. The minor process also uses growth cones but uniquely develops using a mechanism that depends on the clathrin adaptor molecule UNC-101. Together with the guidance of the M2 neuron, this is the second case of a pharyngeal neuron establishing one of its processes using an unexpected mechanism. BioMed Central 2008-04-09 /pmc/articles/PMC2375884/ /pubmed/18400083 http://dx.doi.org/10.1186/1471-213X-8-38 Text en Copyright © 2008 Axäng et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Axäng, Claes
Rauthan, Manish
Hall, David H
Pilon, Marc
Developmental genetics of the C. elegans pharyngeal neurons NSML and NSMR
title Developmental genetics of the C. elegans pharyngeal neurons NSML and NSMR
title_full Developmental genetics of the C. elegans pharyngeal neurons NSML and NSMR
title_fullStr Developmental genetics of the C. elegans pharyngeal neurons NSML and NSMR
title_full_unstemmed Developmental genetics of the C. elegans pharyngeal neurons NSML and NSMR
title_short Developmental genetics of the C. elegans pharyngeal neurons NSML and NSMR
title_sort developmental genetics of the c. elegans pharyngeal neurons nsml and nsmr
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375884/
https://www.ncbi.nlm.nih.gov/pubmed/18400083
http://dx.doi.org/10.1186/1471-213X-8-38
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