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MicroRNA-Dependent Control of Sensory Neuron Function Regulates Posture Behavior in Drosophila
All what we see, touch, hear, taste, or smell must first be detected by the sensory elements of our nervous system. Sensory neurons, therefore, represent a critical component in all neural circuits and their correct function is essential for the generation of behavior and adaptation to the environme...
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Published in: | The Journal of neuroscience 2021-10, Vol.41 (40), p.8297-8308 |
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description | All what we see, touch, hear, taste, or smell must first be detected by the sensory elements of our nervous system. Sensory neurons, therefore, represent a critical component in all neural circuits and their correct function is essential for the generation of behavior and adaptation to the environment. Here, we report that the evolutionarily-conserved microRNA (miRNA)
plays a key behavioral role in
through effects on the function of larval sensory neurons. Several independent experiments (in 50:50 male:female populations) support this finding: first, miRNA expression analysis, via reporter expression and fluorescent-activated cell sorting (FACS)-quantitative PCR (qPCR) analysis, demonstrate
expression in larval sensory neurons. Second, behavioral tests in
null mutants show defects in self-righting, an innate and evolutionarily conserved posture-control behavior that allows larvae to rectify their position if turned upside-down. Third, competitive inhibition of
in sensory neurons using a
"sponge" leads to self-righting defects. Fourth, systematic analysis of sensory neurons in
mutants shows no detectable morphologic defects in their stereotypic pattern, while genetically-encoded calcium sensors expressed in the sensory domain reveal a reduction in neural activity in
mutants. Fifth,
null mutants show reduced "touch-response" behavior and a compromised response to sound, both characteristic of larval sensory deficits. Furthermore, bioinformatic miRNA target analysis, gene expression assays, and behavioral phenocopy experiments suggest that
might exert its effects, at least in part, through repression of the basic helix-loop-helix (bHLH) transcription factor
Altogether, our study suggests a model in which miRNA-dependent control of transcription factor expression affects sensory function and behavior.
Sensory neurons are key to neural circuit function, but how these neurons acquire their specific properties is not well understood. Here, we examine this problem, focusing on the roles played by microRNAs (miRNAs). Using
, we demonstrate that the evolutionarily-conserved miRNA
controls sensory neuron function allowing the animal to perform an adaptive, elaborate three-dimensional movement. Our work thus shows that microRNAs can control complex motor behaviors by modulating sensory neuron physiology, and suggests that similar miRNA-dependent mechanisms may operate in other species. The work contributes to advance the understanding of the molecular basis of behavio |
doi_str_mv | 10.1523/JNEUROSCI.0081-21.2021 |
format | article |
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plays a key behavioral role in
through effects on the function of larval sensory neurons. Several independent experiments (in 50:50 male:female populations) support this finding: first, miRNA expression analysis, via reporter expression and fluorescent-activated cell sorting (FACS)-quantitative PCR (qPCR) analysis, demonstrate
expression in larval sensory neurons. Second, behavioral tests in
null mutants show defects in self-righting, an innate and evolutionarily conserved posture-control behavior that allows larvae to rectify their position if turned upside-down. Third, competitive inhibition of
in sensory neurons using a
"sponge" leads to self-righting defects. Fourth, systematic analysis of sensory neurons in
mutants shows no detectable morphologic defects in their stereotypic pattern, while genetically-encoded calcium sensors expressed in the sensory domain reveal a reduction in neural activity in
mutants. Fifth,
null mutants show reduced "touch-response" behavior and a compromised response to sound, both characteristic of larval sensory deficits. Furthermore, bioinformatic miRNA target analysis, gene expression assays, and behavioral phenocopy experiments suggest that
might exert its effects, at least in part, through repression of the basic helix-loop-helix (bHLH) transcription factor
Altogether, our study suggests a model in which miRNA-dependent control of transcription factor expression affects sensory function and behavior.
Sensory neurons are key to neural circuit function, but how these neurons acquire their specific properties is not well understood. Here, we examine this problem, focusing on the roles played by microRNAs (miRNAs). Using
, we demonstrate that the evolutionarily-conserved miRNA
controls sensory neuron function allowing the animal to perform an adaptive, elaborate three-dimensional movement. Our work thus shows that microRNAs can control complex motor behaviors by modulating sensory neuron physiology, and suggests that similar miRNA-dependent mechanisms may operate in other species. The work contributes to advance the understanding of the molecular basis of behavior and the biological roles of microRNAs within the nervous system.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/JNEUROSCI.0081-21.2021</identifier><identifier>PMID: 34417328</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Adaptive control ; Animals ; Behavior ; Circuits ; Critical components ; Defects ; Drosophila ; Drosophila melanogaster ; Evolution ; Female ; Flow cytometry ; Fluorescence ; Fruit flies ; Gene expression ; Helix-loop-helix proteins (basic) ; Insects ; Larvae ; Male ; MicroRNAs ; MicroRNAs - biosynthesis ; MicroRNAs - genetics ; miRNA ; Motor task performance ; Movement - physiology ; Mutants ; Nervous system ; Neural networks ; Neurons ; Olfaction ; Position sensing ; Posture ; Posture - physiology ; Reflex, Righting - physiology ; Ribonucleic acid ; RNA ; Sensory evaluation ; Sensory neurons ; Sensory properties ; Sensory Receptor Cells - physiology ; Smell ; Three dimensional motion ; Touch ; Transcription factors</subject><ispartof>The Journal of neuroscience, 2021-10, Vol.41 (40), p.8297-8308</ispartof><rights>Copyright © 2021 Klann et al.</rights><rights>Copyright Society for Neuroscience Oct 6, 2021</rights><rights>Copyright © 2021 Klann et al. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-6659847392f99bbca25a67908db089e79ee705e866a46007be10603afb2b2c793</citedby><orcidid>0000-0001-5761-348X ; 0000-0001-6433-4577</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496190/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496190/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34417328$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Klann, Marleen</creatorcontrib><creatorcontrib>Issa, A Raouf</creatorcontrib><creatorcontrib>Pinho, Sofia</creatorcontrib><creatorcontrib>Alonso, Claudio R</creatorcontrib><title>MicroRNA-Dependent Control of Sensory Neuron Function Regulates Posture Behavior in Drosophila</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>All what we see, touch, hear, taste, or smell must first be detected by the sensory elements of our nervous system. Sensory neurons, therefore, represent a critical component in all neural circuits and their correct function is essential for the generation of behavior and adaptation to the environment. Here, we report that the evolutionarily-conserved microRNA (miRNA)
plays a key behavioral role in
through effects on the function of larval sensory neurons. Several independent experiments (in 50:50 male:female populations) support this finding: first, miRNA expression analysis, via reporter expression and fluorescent-activated cell sorting (FACS)-quantitative PCR (qPCR) analysis, demonstrate
expression in larval sensory neurons. Second, behavioral tests in
null mutants show defects in self-righting, an innate and evolutionarily conserved posture-control behavior that allows larvae to rectify their position if turned upside-down. Third, competitive inhibition of
in sensory neurons using a
"sponge" leads to self-righting defects. Fourth, systematic analysis of sensory neurons in
mutants shows no detectable morphologic defects in their stereotypic pattern, while genetically-encoded calcium sensors expressed in the sensory domain reveal a reduction in neural activity in
mutants. Fifth,
null mutants show reduced "touch-response" behavior and a compromised response to sound, both characteristic of larval sensory deficits. Furthermore, bioinformatic miRNA target analysis, gene expression assays, and behavioral phenocopy experiments suggest that
might exert its effects, at least in part, through repression of the basic helix-loop-helix (bHLH) transcription factor
Altogether, our study suggests a model in which miRNA-dependent control of transcription factor expression affects sensory function and behavior.
Sensory neurons are key to neural circuit function, but how these neurons acquire their specific properties is not well understood. Here, we examine this problem, focusing on the roles played by microRNAs (miRNAs). Using
, we demonstrate that the evolutionarily-conserved miRNA
controls sensory neuron function allowing the animal to perform an adaptive, elaborate three-dimensional movement. Our work thus shows that microRNAs can control complex motor behaviors by modulating sensory neuron physiology, and suggests that similar miRNA-dependent mechanisms may operate in other species. The work contributes to advance the understanding of the molecular basis of behavior and the biological roles of microRNAs within the nervous system.</description><subject>Adaptive control</subject><subject>Animals</subject><subject>Behavior</subject><subject>Circuits</subject><subject>Critical components</subject><subject>Defects</subject><subject>Drosophila</subject><subject>Drosophila melanogaster</subject><subject>Evolution</subject><subject>Female</subject><subject>Flow cytometry</subject><subject>Fluorescence</subject><subject>Fruit flies</subject><subject>Gene expression</subject><subject>Helix-loop-helix proteins (basic)</subject><subject>Insects</subject><subject>Larvae</subject><subject>Male</subject><subject>MicroRNAs</subject><subject>MicroRNAs - biosynthesis</subject><subject>MicroRNAs - genetics</subject><subject>miRNA</subject><subject>Motor task performance</subject><subject>Movement - physiology</subject><subject>Mutants</subject><subject>Nervous system</subject><subject>Neural networks</subject><subject>Neurons</subject><subject>Olfaction</subject><subject>Position sensing</subject><subject>Posture</subject><subject>Posture - physiology</subject><subject>Reflex, Righting - physiology</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Sensory evaluation</subject><subject>Sensory neurons</subject><subject>Sensory properties</subject><subject>Sensory Receptor Cells - physiology</subject><subject>Smell</subject><subject>Three dimensional motion</subject><subject>Touch</subject><subject>Transcription factors</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpdkV9rFDEUxYModq1-hRLwxZdZk5tM_rwIddtqpW5la18Nmdk73SmzyTaZKfTbm9K6qBC4gfu7h3vuIeSIszmvQXz8tjy9Xl1eLc7njBleAZ8DA_6CzErXViAZf0lmDDSrlNTygLzJ-ZYxphnXr8mBkJJrAWZGfn3v2xRXy-PqBHcY1hhGuohhTHGgsaNXGHJMD3SJU4qBnk2hHfvyWeHNNPgRM_0R8zglpJ9x4-_7mGgf6EmKOe42_eDfkledHzK-e66H5Prs9Ofia3Vx-eV8cXxRtVLCWClVWyO1sNBZ2zSth9orbZlZN8xY1BZRsxqNUl6q4qJBzhQTvmuggVZbcUg-PenupmaL67bYSH5wu9RvfXpw0ffu307oN-4m3jsjreKWFYEPzwIp3k2YR7ftc4vD4APGKTuolZDAhYGCvv8PvY1TCsVeoQwAt7LWhVJPVDlvzgm7_TKcuccI3T5C9xihg_JKhGXw6G8r-7E_mYnfWhuYzA</recordid><startdate>20211006</startdate><enddate>20211006</enddate><creator>Klann, Marleen</creator><creator>Issa, A Raouf</creator><creator>Pinho, Sofia</creator><creator>Alonso, Claudio R</creator><general>Society for Neuroscience</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5761-348X</orcidid><orcidid>https://orcid.org/0000-0001-6433-4577</orcidid></search><sort><creationdate>20211006</creationdate><title>MicroRNA-Dependent Control of Sensory Neuron Function Regulates Posture Behavior in Drosophila</title><author>Klann, Marleen ; Issa, A Raouf ; Pinho, Sofia ; Alonso, Claudio R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-6659847392f99bbca25a67908db089e79ee705e866a46007be10603afb2b2c793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adaptive control</topic><topic>Animals</topic><topic>Behavior</topic><topic>Circuits</topic><topic>Critical components</topic><topic>Defects</topic><topic>Drosophila</topic><topic>Drosophila melanogaster</topic><topic>Evolution</topic><topic>Female</topic><topic>Flow cytometry</topic><topic>Fluorescence</topic><topic>Fruit flies</topic><topic>Gene expression</topic><topic>Helix-loop-helix proteins (basic)</topic><topic>Insects</topic><topic>Larvae</topic><topic>Male</topic><topic>MicroRNAs</topic><topic>MicroRNAs - biosynthesis</topic><topic>MicroRNAs - genetics</topic><topic>miRNA</topic><topic>Motor task performance</topic><topic>Movement - physiology</topic><topic>Mutants</topic><topic>Nervous system</topic><topic>Neural networks</topic><topic>Neurons</topic><topic>Olfaction</topic><topic>Position sensing</topic><topic>Posture</topic><topic>Posture - physiology</topic><topic>Reflex, Righting - physiology</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Sensory evaluation</topic><topic>Sensory neurons</topic><topic>Sensory properties</topic><topic>Sensory Receptor Cells - physiology</topic><topic>Smell</topic><topic>Three dimensional motion</topic><topic>Touch</topic><topic>Transcription factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Klann, Marleen</creatorcontrib><creatorcontrib>Issa, A Raouf</creatorcontrib><creatorcontrib>Pinho, Sofia</creatorcontrib><creatorcontrib>Alonso, Claudio R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Klann, Marleen</au><au>Issa, A Raouf</au><au>Pinho, Sofia</au><au>Alonso, Claudio R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MicroRNA-Dependent Control of Sensory Neuron Function Regulates Posture Behavior in Drosophila</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2021-10-06</date><risdate>2021</risdate><volume>41</volume><issue>40</issue><spage>8297</spage><epage>8308</epage><pages>8297-8308</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>All what we see, touch, hear, taste, or smell must first be detected by the sensory elements of our nervous system. Sensory neurons, therefore, represent a critical component in all neural circuits and their correct function is essential for the generation of behavior and adaptation to the environment. Here, we report that the evolutionarily-conserved microRNA (miRNA)
plays a key behavioral role in
through effects on the function of larval sensory neurons. Several independent experiments (in 50:50 male:female populations) support this finding: first, miRNA expression analysis, via reporter expression and fluorescent-activated cell sorting (FACS)-quantitative PCR (qPCR) analysis, demonstrate
expression in larval sensory neurons. Second, behavioral tests in
null mutants show defects in self-righting, an innate and evolutionarily conserved posture-control behavior that allows larvae to rectify their position if turned upside-down. Third, competitive inhibition of
in sensory neurons using a
"sponge" leads to self-righting defects. Fourth, systematic analysis of sensory neurons in
mutants shows no detectable morphologic defects in their stereotypic pattern, while genetically-encoded calcium sensors expressed in the sensory domain reveal a reduction in neural activity in
mutants. Fifth,
null mutants show reduced "touch-response" behavior and a compromised response to sound, both characteristic of larval sensory deficits. Furthermore, bioinformatic miRNA target analysis, gene expression assays, and behavioral phenocopy experiments suggest that
might exert its effects, at least in part, through repression of the basic helix-loop-helix (bHLH) transcription factor
Altogether, our study suggests a model in which miRNA-dependent control of transcription factor expression affects sensory function and behavior.
Sensory neurons are key to neural circuit function, but how these neurons acquire their specific properties is not well understood. Here, we examine this problem, focusing on the roles played by microRNAs (miRNAs). Using
, we demonstrate that the evolutionarily-conserved miRNA
controls sensory neuron function allowing the animal to perform an adaptive, elaborate three-dimensional movement. Our work thus shows that microRNAs can control complex motor behaviors by modulating sensory neuron physiology, and suggests that similar miRNA-dependent mechanisms may operate in other species. The work contributes to advance the understanding of the molecular basis of behavior and the biological roles of microRNAs within the nervous system.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>34417328</pmid><doi>10.1523/JNEUROSCI.0081-21.2021</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-5761-348X</orcidid><orcidid>https://orcid.org/0000-0001-6433-4577</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adaptive control Animals Behavior Circuits Critical components Defects Drosophila Drosophila melanogaster Evolution Female Flow cytometry Fluorescence Fruit flies Gene expression Helix-loop-helix proteins (basic) Insects Larvae Male MicroRNAs MicroRNAs - biosynthesis MicroRNAs - genetics miRNA Motor task performance Movement - physiology Mutants Nervous system Neural networks Neurons Olfaction Position sensing Posture Posture - physiology Reflex, Righting - physiology Ribonucleic acid RNA Sensory evaluation Sensory neurons Sensory properties Sensory Receptor Cells - physiology Smell Three dimensional motion Touch Transcription factors |
title | MicroRNA-Dependent Control of Sensory Neuron Function Regulates Posture Behavior in Drosophila |
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