Cargando…

The MicroRNA mir-71 Inhibits Calcium Signaling by Targeting the TIR-1/Sarm1 Adaptor Protein to Control Stochastic L/R Neuronal Asymmetry in C. elegans

The Caenorhabditis elegans left and right AWC olfactory neurons communicate to establish stochastic asymmetric identities, AWC(ON) and AWC(OFF), by inhibiting a calcium-mediated signaling pathway in the future AWC(ON) cell. NSY-4/claudin-like protein and NSY-5/innexin gap junction protein are the tw...

Descripción completa

Detalles Bibliográficos
Autores principales: Hsieh, Yi-Wen, Chang, Chieh, Chuang, Chiou-Fen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410857/
https://www.ncbi.nlm.nih.gov/pubmed/22876200
http://dx.doi.org/10.1371/journal.pgen.1002864
_version_ 1782239772906881024
author Hsieh, Yi-Wen
Chang, Chieh
Chuang, Chiou-Fen
author_facet Hsieh, Yi-Wen
Chang, Chieh
Chuang, Chiou-Fen
author_sort Hsieh, Yi-Wen
collection PubMed
description The Caenorhabditis elegans left and right AWC olfactory neurons communicate to establish stochastic asymmetric identities, AWC(ON) and AWC(OFF), by inhibiting a calcium-mediated signaling pathway in the future AWC(ON) cell. NSY-4/claudin-like protein and NSY-5/innexin gap junction protein are the two parallel signals that antagonize the calcium signaling pathway to induce the AWC(ON) fate. However, it is not known how the calcium signaling pathway is downregulated by nsy-4 and nsy-5 in the AWC(ON) cell. Here we identify a microRNA, mir-71, that represses the TIR-1/Sarm1 adaptor protein in the calcium signaling pathway to promote the AWC(ON) identity. Similar to tir-1 loss-of-function mutants, overexpression of mir-71 generates two AWC(ON) neurons. tir-1 expression is downregulated through its 3′ UTR in AWC(ON), in which mir-71 is expressed at a higher level than in AWC(OFF). In addition, mir-71 is sufficient to inhibit tir-1 expression in AWC through the mir-71 complementary site in the tir-1 3′ UTR. Our genetic studies suggest that mir-71 acts downstream of nsy-4 and nsy-5 to promote the AWC(ON) identity in a cell autonomous manner. Furthermore, the stability of mature mir-71 is dependent on nsy-4 and nsy-5. Together, these results provide insight into the mechanism by which nsy-4 and nsy-5 inhibit calcium signaling to establish stochastic asymmetric AWC differentiation.
format Online
Article
Text
id pubmed-3410857
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-34108572012-08-08 The MicroRNA mir-71 Inhibits Calcium Signaling by Targeting the TIR-1/Sarm1 Adaptor Protein to Control Stochastic L/R Neuronal Asymmetry in C. elegans Hsieh, Yi-Wen Chang, Chieh Chuang, Chiou-Fen PLoS Genet Research Article The Caenorhabditis elegans left and right AWC olfactory neurons communicate to establish stochastic asymmetric identities, AWC(ON) and AWC(OFF), by inhibiting a calcium-mediated signaling pathway in the future AWC(ON) cell. NSY-4/claudin-like protein and NSY-5/innexin gap junction protein are the two parallel signals that antagonize the calcium signaling pathway to induce the AWC(ON) fate. However, it is not known how the calcium signaling pathway is downregulated by nsy-4 and nsy-5 in the AWC(ON) cell. Here we identify a microRNA, mir-71, that represses the TIR-1/Sarm1 adaptor protein in the calcium signaling pathway to promote the AWC(ON) identity. Similar to tir-1 loss-of-function mutants, overexpression of mir-71 generates two AWC(ON) neurons. tir-1 expression is downregulated through its 3′ UTR in AWC(ON), in which mir-71 is expressed at a higher level than in AWC(OFF). In addition, mir-71 is sufficient to inhibit tir-1 expression in AWC through the mir-71 complementary site in the tir-1 3′ UTR. Our genetic studies suggest that mir-71 acts downstream of nsy-4 and nsy-5 to promote the AWC(ON) identity in a cell autonomous manner. Furthermore, the stability of mature mir-71 is dependent on nsy-4 and nsy-5. Together, these results provide insight into the mechanism by which nsy-4 and nsy-5 inhibit calcium signaling to establish stochastic asymmetric AWC differentiation. Public Library of Science 2012-08-02 /pmc/articles/PMC3410857/ /pubmed/22876200 http://dx.doi.org/10.1371/journal.pgen.1002864 Text en Hsieh et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hsieh, Yi-Wen
Chang, Chieh
Chuang, Chiou-Fen
The MicroRNA mir-71 Inhibits Calcium Signaling by Targeting the TIR-1/Sarm1 Adaptor Protein to Control Stochastic L/R Neuronal Asymmetry in C. elegans
title The MicroRNA mir-71 Inhibits Calcium Signaling by Targeting the TIR-1/Sarm1 Adaptor Protein to Control Stochastic L/R Neuronal Asymmetry in C. elegans
title_full The MicroRNA mir-71 Inhibits Calcium Signaling by Targeting the TIR-1/Sarm1 Adaptor Protein to Control Stochastic L/R Neuronal Asymmetry in C. elegans
title_fullStr The MicroRNA mir-71 Inhibits Calcium Signaling by Targeting the TIR-1/Sarm1 Adaptor Protein to Control Stochastic L/R Neuronal Asymmetry in C. elegans
title_full_unstemmed The MicroRNA mir-71 Inhibits Calcium Signaling by Targeting the TIR-1/Sarm1 Adaptor Protein to Control Stochastic L/R Neuronal Asymmetry in C. elegans
title_short The MicroRNA mir-71 Inhibits Calcium Signaling by Targeting the TIR-1/Sarm1 Adaptor Protein to Control Stochastic L/R Neuronal Asymmetry in C. elegans
title_sort microrna mir-71 inhibits calcium signaling by targeting the tir-1/sarm1 adaptor protein to control stochastic l/r neuronal asymmetry in c. elegans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410857/
https://www.ncbi.nlm.nih.gov/pubmed/22876200
http://dx.doi.org/10.1371/journal.pgen.1002864
work_keys_str_mv AT hsiehyiwen themicrornamir71inhibitscalciumsignalingbytargetingthetir1sarm1adaptorproteintocontrolstochasticlrneuronalasymmetryincelegans
AT changchieh themicrornamir71inhibitscalciumsignalingbytargetingthetir1sarm1adaptorproteintocontrolstochasticlrneuronalasymmetryincelegans
AT chuangchioufen themicrornamir71inhibitscalciumsignalingbytargetingthetir1sarm1adaptorproteintocontrolstochasticlrneuronalasymmetryincelegans
AT hsiehyiwen micrornamir71inhibitscalciumsignalingbytargetingthetir1sarm1adaptorproteintocontrolstochasticlrneuronalasymmetryincelegans
AT changchieh micrornamir71inhibitscalciumsignalingbytargetingthetir1sarm1adaptorproteintocontrolstochasticlrneuronalasymmetryincelegans
AT chuangchioufen micrornamir71inhibitscalciumsignalingbytargetingthetir1sarm1adaptorproteintocontrolstochasticlrneuronalasymmetryincelegans