Tyrosine hydroxylase messenger RNA corroborates protein localization in the nervous system of the pond snail, Lymnaea stagnalis
Catecholaminergic neurons are abundant in molluscs and are involved in a variety of behaviors such as feeding, respiration, learning, and locomotion. However, previous identification of these neurons has relied almost exclusively on immunohistochemistry using antibodies, which have not been fully va...
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Veröffentlicht in: | Invertebrate biology 2022-06, Vol.141 (2), p.n/a |
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description | Catecholaminergic neurons are abundant in molluscs and are involved in a variety of behaviors such as feeding, respiration, learning, and locomotion. However, previous identification of these neurons has relied almost exclusively on immunohistochemistry using antibodies, which have not been fully validated for use in molluscs. We employed tissue‐specific quantitative PCR in adults of Lymnaea stagnalis (a pulmonate gastropod) and whole‐mount in situ hybridization in larvae to both quantify and visualize messenger RNA of the catecholamine synthesis enzyme, tyrosine hydroxylase (TH). TH messenger RNA was found to localize primarily in the foot and the central nervous system, with smaller quantities present in the cephalic sensory organs. Additionally, we performed western blots that validated a popular antibody used as a marker for catecholaminergic neurons in molluscs. Taken together, these data indicate that TH messenger RNA is present in the central and peripheral nervous system of L. stagnalis and support the specificity of past immunohistochemical labeling of the TH protein. These findings have potentially broad implications, given the wide range of biological processes that have been studied in L. stagnalis. |
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However, previous identification of these neurons has relied almost exclusively on immunohistochemistry using antibodies, which have not been fully validated for use in molluscs. We employed tissue‐specific quantitative PCR in adults of Lymnaea stagnalis (a pulmonate gastropod) and whole‐mount in situ hybridization in larvae to both quantify and visualize messenger RNA of the catecholamine synthesis enzyme, tyrosine hydroxylase (TH). TH messenger RNA was found to localize primarily in the foot and the central nervous system, with smaller quantities present in the cephalic sensory organs. Additionally, we performed western blots that validated a popular antibody used as a marker for catecholaminergic neurons in molluscs. Taken together, these data indicate that TH messenger RNA is present in the central and peripheral nervous system of L. stagnalis and support the specificity of past immunohistochemical labeling of the TH protein. These findings have potentially broad implications, given the wide range of biological processes that have been studied in L. stagnalis.</description><identifier>ISSN: 1077-8306</identifier><identifier>EISSN: 1744-7410</identifier><identifier>DOI: 10.1111/ivb.12367</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Antibodies ; Biological activity ; Body organs ; Catecholamine ; Catecholamines ; Central nervous system ; Feeding behavior ; Hybridization ; Hydroxylase ; Immunohistochemistry ; Larvae ; Localization ; Locomotion ; Lymnaea stagnalis ; Marine molluscs ; mollusc ; Mollusca ; Mollusks ; Nervous system ; neuroanatomy ; Neurons ; nucleic acid localization ; Nucleic acids ; Nucleotide sequence ; Organs ; PCR ; Peripheral nervous system ; Proteins ; RNA ; Sense organs ; Specificity ; Transcription ; Tyrosine ; Tyrosine 3-monooxygenase ; Western blotting</subject><ispartof>Invertebrate biology, 2022-06, Vol.141 (2), p.n/a</ispartof><rights>2022 The American Microscopical Society LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2977-e72c5fdd64cdfe7c8099419163798b66b406c92c3ebd933b1c5a73941709af163</citedby><cites>FETCH-LOGICAL-c2977-e72c5fdd64cdfe7c8099419163798b66b406c92c3ebd933b1c5a73941709af163</cites><orcidid>0000-0003-0971-7588 ; 0000-0001-9045-381X ; 0000-0002-9846-0923 ; 0000-0003-0751-2132 ; 0000-0003-3395-2377</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fivb.12367$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fivb.12367$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Young, Alexander P.</creatorcontrib><creatorcontrib>Beach, Griffin A.</creatorcontrib><creatorcontrib>Croll, Roger P.</creatorcontrib><creatorcontrib>Jackson, Daniel J.</creatorcontrib><creatorcontrib>Wyeth, Russell C.</creatorcontrib><title>Tyrosine hydroxylase messenger RNA corroborates protein localization in the nervous system of the pond snail, Lymnaea stagnalis</title><title>Invertebrate biology</title><description>Catecholaminergic neurons are abundant in molluscs and are involved in a variety of behaviors such as feeding, respiration, learning, and locomotion. However, previous identification of these neurons has relied almost exclusively on immunohistochemistry using antibodies, which have not been fully validated for use in molluscs. We employed tissue‐specific quantitative PCR in adults of Lymnaea stagnalis (a pulmonate gastropod) and whole‐mount in situ hybridization in larvae to both quantify and visualize messenger RNA of the catecholamine synthesis enzyme, tyrosine hydroxylase (TH). TH messenger RNA was found to localize primarily in the foot and the central nervous system, with smaller quantities present in the cephalic sensory organs. Additionally, we performed western blots that validated a popular antibody used as a marker for catecholaminergic neurons in molluscs. Taken together, these data indicate that TH messenger RNA is present in the central and peripheral nervous system of L. stagnalis and support the specificity of past immunohistochemical labeling of the TH protein. These findings have potentially broad implications, given the wide range of biological processes that have been studied in L. stagnalis.</description><subject>Antibodies</subject><subject>Biological activity</subject><subject>Body organs</subject><subject>Catecholamine</subject><subject>Catecholamines</subject><subject>Central nervous system</subject><subject>Feeding behavior</subject><subject>Hybridization</subject><subject>Hydroxylase</subject><subject>Immunohistochemistry</subject><subject>Larvae</subject><subject>Localization</subject><subject>Locomotion</subject><subject>Lymnaea stagnalis</subject><subject>Marine molluscs</subject><subject>mollusc</subject><subject>Mollusca</subject><subject>Mollusks</subject><subject>Nervous system</subject><subject>neuroanatomy</subject><subject>Neurons</subject><subject>nucleic acid localization</subject><subject>Nucleic acids</subject><subject>Nucleotide sequence</subject><subject>Organs</subject><subject>PCR</subject><subject>Peripheral nervous system</subject><subject>Proteins</subject><subject>RNA</subject><subject>Sense organs</subject><subject>Specificity</subject><subject>Transcription</subject><subject>Tyrosine</subject><subject>Tyrosine 3-monooxygenase</subject><subject>Western blotting</subject><issn>1077-8306</issn><issn>1744-7410</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kF1LwzAUhosoOKcX_oOAV4LdkjZL2ss5_BgMBZneljQ93TraZOZ003rjXzeu3pqb5ITnPbw8QXDJ6Ij5M672-YhFsZBHwYBJzkPJGT32byplmMRUnAZniBtKacK4GATfy85ZrAyQdVc4-9nVCoE0gAhmBY68PE2Jts7Z3DrVApKtsy1UhtRWq7r6Um1lDfFzuwZiwO3tDgl22EJDbHn43VpTEDSqqm_IomuMAkWwVSvj83genJSqRrj4u4fB6_3dcvYYLp4f5rPpItRR6puDjPSkLArBdVGC1AlNU85SJmKZJrkQOadCp5GOIS_SOM6ZnigZe0TSVJUeGwZX_V7f_30H2GYbu3O-AmaRkIJz6X146rqntJeCDsps66pGuS5jNPv1m3m_2cGvZ8c9-1HV0P0PZvO32z7xA8hkfpk</recordid><startdate>202206</startdate><enddate>202206</enddate><creator>Young, Alexander P.</creator><creator>Beach, Griffin A.</creator><creator>Croll, Roger P.</creator><creator>Jackson, Daniel J.</creator><creator>Wyeth, Russell C.</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7TK</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>L.G</scope><scope>P64</scope><orcidid>https://orcid.org/0000-0003-0971-7588</orcidid><orcidid>https://orcid.org/0000-0001-9045-381X</orcidid><orcidid>https://orcid.org/0000-0002-9846-0923</orcidid><orcidid>https://orcid.org/0000-0003-0751-2132</orcidid><orcidid>https://orcid.org/0000-0003-3395-2377</orcidid></search><sort><creationdate>202206</creationdate><title>Tyrosine hydroxylase messenger RNA corroborates protein localization in the nervous system of the pond snail, Lymnaea stagnalis</title><author>Young, Alexander P. ; Beach, Griffin A. ; Croll, Roger P. ; Jackson, Daniel J. ; Wyeth, Russell C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2977-e72c5fdd64cdfe7c8099419163798b66b406c92c3ebd933b1c5a73941709af163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antibodies</topic><topic>Biological activity</topic><topic>Body organs</topic><topic>Catecholamine</topic><topic>Catecholamines</topic><topic>Central nervous system</topic><topic>Feeding behavior</topic><topic>Hybridization</topic><topic>Hydroxylase</topic><topic>Immunohistochemistry</topic><topic>Larvae</topic><topic>Localization</topic><topic>Locomotion</topic><topic>Lymnaea stagnalis</topic><topic>Marine molluscs</topic><topic>mollusc</topic><topic>Mollusca</topic><topic>Mollusks</topic><topic>Nervous system</topic><topic>neuroanatomy</topic><topic>Neurons</topic><topic>nucleic acid localization</topic><topic>Nucleic acids</topic><topic>Nucleotide sequence</topic><topic>Organs</topic><topic>PCR</topic><topic>Peripheral nervous system</topic><topic>Proteins</topic><topic>RNA</topic><topic>Sense organs</topic><topic>Specificity</topic><topic>Transcription</topic><topic>Tyrosine</topic><topic>Tyrosine 3-monooxygenase</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Young, Alexander P.</creatorcontrib><creatorcontrib>Beach, Griffin A.</creatorcontrib><creatorcontrib>Croll, Roger P.</creatorcontrib><creatorcontrib>Jackson, Daniel J.</creatorcontrib><creatorcontrib>Wyeth, Russell C.</creatorcontrib><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Invertebrate biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Young, Alexander P.</au><au>Beach, Griffin A.</au><au>Croll, Roger P.</au><au>Jackson, Daniel J.</au><au>Wyeth, Russell C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tyrosine hydroxylase messenger RNA corroborates protein localization in the nervous system of the pond snail, Lymnaea stagnalis</atitle><jtitle>Invertebrate biology</jtitle><date>2022-06</date><risdate>2022</risdate><volume>141</volume><issue>2</issue><epage>n/a</epage><issn>1077-8306</issn><eissn>1744-7410</eissn><abstract>Catecholaminergic neurons are abundant in molluscs and are involved in a variety of behaviors such as feeding, respiration, learning, and locomotion. However, previous identification of these neurons has relied almost exclusively on immunohistochemistry using antibodies, which have not been fully validated for use in molluscs. We employed tissue‐specific quantitative PCR in adults of Lymnaea stagnalis (a pulmonate gastropod) and whole‐mount in situ hybridization in larvae to both quantify and visualize messenger RNA of the catecholamine synthesis enzyme, tyrosine hydroxylase (TH). TH messenger RNA was found to localize primarily in the foot and the central nervous system, with smaller quantities present in the cephalic sensory organs. Additionally, we performed western blots that validated a popular antibody used as a marker for catecholaminergic neurons in molluscs. Taken together, these data indicate that TH messenger RNA is present in the central and peripheral nervous system of L. stagnalis and support the specificity of past immunohistochemical labeling of the TH protein. 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subjects | Antibodies Biological activity Body organs Catecholamine Catecholamines Central nervous system Feeding behavior Hybridization Hydroxylase Immunohistochemistry Larvae Localization Locomotion Lymnaea stagnalis Marine molluscs mollusc Mollusca Mollusks Nervous system neuroanatomy Neurons nucleic acid localization Nucleic acids Nucleotide sequence Organs PCR Peripheral nervous system Proteins RNA Sense organs Specificity Transcription Tyrosine Tyrosine 3-monooxygenase Western blotting |
title | Tyrosine hydroxylase messenger RNA corroborates protein localization in the nervous system of the pond snail, Lymnaea stagnalis |
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