The CATP-8/P5A-type ATPase functions in multiple pathways during neuronal patterning
The assembly of neuronal circuits involves the migrations of neurons from their place of birth to their final location in the nervous system, as well as the coordinated growth and patterning of axons and dendrites. In screens for genes required for patterning of the nervous system, we identified the...
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description | The assembly of neuronal circuits involves the migrations of neurons from their place of birth to their final location in the nervous system, as well as the coordinated growth and patterning of axons and dendrites. In screens for genes required for patterning of the nervous system, we identified the catp-8/P5A-ATPase as an important regulator of neural patterning. P5A-ATPases are part of the P-type ATPases, a family of proteins known to serve a conserved function as transporters of ions, lipids and polyamines in unicellular eukaryotes, plants, and humans. While the function of many P-type ATPases is relatively well understood, the function of P5A-ATPases in metazoans remained elusive. We show here, that the Caenorhabditis elegans ortholog catp-8/P5A-ATPase is required for defined aspects of nervous system development. Specifically, the catp-8/P5A-ATPase serves functions in shaping the elaborately sculpted dendritic trees of somatosensory PVD neurons. Moreover, catp-8/P5A-ATPase is required for axonal guidance and repulsion at the midline, as well as embryonic and postembryonic neuronal migrations. Interestingly, not all axons at the midline require catp-8/P5A-ATPase, although the axons run in the same fascicles and navigate the same space. Similarly, not all neuronal migrations require catp-8/P5A-ATPase. A CATP-8/P5A-ATPase reporter is localized to the ER in most, if not all, tissues and catp-8/P5A-ATPase can function both cell-autonomously and non-autonomously to regulate neuronal development. Genetic analyses establish that catp-8/P5A-ATPase can function in multiple pathways, including the Menorin pathway, previously shown to control dendritic patterning in PVD, and Wnt signaling, which functions to control neuronal migrations. Lastly, we show that catp-8/P5A-ATPase is required for localizing select transmembrane proteins necessary for dendrite morphogenesis. Collectively, our studies suggest that catp-8/P5A-ATPase serves diverse, yet specific, roles in different genetic pathways and may be involved in the regulation or localization of transmembrane and secreted proteins to specific subcellular compartments. |
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H ; Trivedi, Meera ; Freund, Jenna ; Salazar, Christopher J ; Rahman, Maisha ; Ramirez-Suarez, Nelson J ; Lee, Garrett ; Wang, Yu ; Grant, Barth D ; Bülow, Hannes E</creator><contributor>Benard, Claire Y.</contributor><creatorcontrib>Tang, Leo T. H ; Trivedi, Meera ; Freund, Jenna ; Salazar, Christopher J ; Rahman, Maisha ; Ramirez-Suarez, Nelson J ; Lee, Garrett ; Wang, Yu ; Grant, Barth D ; Bülow, Hannes E ; Benard, Claire Y.</creatorcontrib><description>The assembly of neuronal circuits involves the migrations of neurons from their place of birth to their final location in the nervous system, as well as the coordinated growth and patterning of axons and dendrites. In screens for genes required for patterning of the nervous system, we identified the catp-8/P5A-ATPase as an important regulator of neural patterning. P5A-ATPases are part of the P-type ATPases, a family of proteins known to serve a conserved function as transporters of ions, lipids and polyamines in unicellular eukaryotes, plants, and humans. While the function of many P-type ATPases is relatively well understood, the function of P5A-ATPases in metazoans remained elusive. We show here, that the Caenorhabditis elegans ortholog catp-8/P5A-ATPase is required for defined aspects of nervous system development. Specifically, the catp-8/P5A-ATPase serves functions in shaping the elaborately sculpted dendritic trees of somatosensory PVD neurons. Moreover, catp-8/P5A-ATPase is required for axonal guidance and repulsion at the midline, as well as embryonic and postembryonic neuronal migrations. Interestingly, not all axons at the midline require catp-8/P5A-ATPase, although the axons run in the same fascicles and navigate the same space. Similarly, not all neuronal migrations require catp-8/P5A-ATPase. A CATP-8/P5A-ATPase reporter is localized to the ER in most, if not all, tissues and catp-8/P5A-ATPase can function both cell-autonomously and non-autonomously to regulate neuronal development. Genetic analyses establish that catp-8/P5A-ATPase can function in multiple pathways, including the Menorin pathway, previously shown to control dendritic patterning in PVD, and Wnt signaling, which functions to control neuronal migrations. Lastly, we show that catp-8/P5A-ATPase is required for localizing select transmembrane proteins necessary for dendrite morphogenesis. Collectively, our studies suggest that catp-8/P5A-ATPase serves diverse, yet specific, roles in different genetic pathways and may be involved in the regulation or localization of transmembrane and secreted proteins to specific subcellular compartments.</description><identifier>ISSN: 1553-7404</identifier><identifier>ISSN: 1553-7390</identifier><identifier>EISSN: 1553-7404</identifier><identifier>DOI: 10.1371/journal.pgen.1009475</identifier><identifier>PMID: 34197450</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Adenosine triphosphatase ; Amino acids ; Animals ; Axon guidance ; Axonogenesis ; Biology and Life Sciences ; Dendritic branching ; Embryos ; Genetic analysis ; Genetic aspects ; Genetic regulation ; Genetic research ; Genetic screening ; Genomes ; Homeostasis ; Lipids ; Localization ; Membrane proteins ; Membranes ; Morphogenesis ; Mutation ; Nervous system ; Neural circuitry ; Neurological research ; Neurons ; Pattern formation ; Physiological aspects ; Polyamines ; Proteins ; Research and Analysis Methods ; Wnt protein</subject><ispartof>PLoS genetics, 2021-07, Vol.17 (7), p.e1009475-e1009475</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 Tang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 Tang et al 2021 Tang et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c703t-1ccf46bf42d80e39a3dc915f3a5daf10648624cc3a31f499d3e5ac5ad11c89553</citedby><cites>FETCH-LOGICAL-c703t-1ccf46bf42d80e39a3dc915f3a5daf10648624cc3a31f499d3e5ac5ad11c89553</cites><orcidid>0000-0003-1795-0814 ; 0000-0001-7946-2061 ; 0000-0001-9631-0414 ; 0000-0001-5853-3019 ; 0000-0002-9465-2936 ; 0000-0001-5922-9238 ; 0000-0001-8264-8318 ; 0000-0002-5943-8336 ; 0000-0001-7394-860X ; 0000-0002-6271-0572</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/PMC8279360/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8279360/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids></links><search><contributor>Benard, Claire Y.</contributor><creatorcontrib>Tang, Leo T. H</creatorcontrib><creatorcontrib>Trivedi, Meera</creatorcontrib><creatorcontrib>Freund, Jenna</creatorcontrib><creatorcontrib>Salazar, Christopher J</creatorcontrib><creatorcontrib>Rahman, Maisha</creatorcontrib><creatorcontrib>Ramirez-Suarez, Nelson J</creatorcontrib><creatorcontrib>Lee, Garrett</creatorcontrib><creatorcontrib>Wang, Yu</creatorcontrib><creatorcontrib>Grant, Barth D</creatorcontrib><creatorcontrib>Bülow, Hannes E</creatorcontrib><title>The CATP-8/P5A-type ATPase functions in multiple pathways during neuronal patterning</title><title>PLoS genetics</title><description>The assembly of neuronal circuits involves the migrations of neurons from their place of birth to their final location in the nervous system, as well as the coordinated growth and patterning of axons and dendrites. In screens for genes required for patterning of the nervous system, we identified the catp-8/P5A-ATPase as an important regulator of neural patterning. P5A-ATPases are part of the P-type ATPases, a family of proteins known to serve a conserved function as transporters of ions, lipids and polyamines in unicellular eukaryotes, plants, and humans. While the function of many P-type ATPases is relatively well understood, the function of P5A-ATPases in metazoans remained elusive. We show here, that the Caenorhabditis elegans ortholog catp-8/P5A-ATPase is required for defined aspects of nervous system development. Specifically, the catp-8/P5A-ATPase serves functions in shaping the elaborately sculpted dendritic trees of somatosensory PVD neurons. Moreover, catp-8/P5A-ATPase is required for axonal guidance and repulsion at the midline, as well as embryonic and postembryonic neuronal migrations. Interestingly, not all axons at the midline require catp-8/P5A-ATPase, although the axons run in the same fascicles and navigate the same space. Similarly, not all neuronal migrations require catp-8/P5A-ATPase. A CATP-8/P5A-ATPase reporter is localized to the ER in most, if not all, tissues and catp-8/P5A-ATPase can function both cell-autonomously and non-autonomously to regulate neuronal development. Genetic analyses establish that catp-8/P5A-ATPase can function in multiple pathways, including the Menorin pathway, previously shown to control dendritic patterning in PVD, and Wnt signaling, which functions to control neuronal migrations. Lastly, we show that catp-8/P5A-ATPase is required for localizing select transmembrane proteins necessary for dendrite morphogenesis. 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In screens for genes required for patterning of the nervous system, we identified the catp-8/P5A-ATPase as an important regulator of neural patterning. P5A-ATPases are part of the P-type ATPases, a family of proteins known to serve a conserved function as transporters of ions, lipids and polyamines in unicellular eukaryotes, plants, and humans. While the function of many P-type ATPases is relatively well understood, the function of P5A-ATPases in metazoans remained elusive. We show here, that the Caenorhabditis elegans ortholog catp-8/P5A-ATPase is required for defined aspects of nervous system development. Specifically, the catp-8/P5A-ATPase serves functions in shaping the elaborately sculpted dendritic trees of somatosensory PVD neurons. Moreover, catp-8/P5A-ATPase is required for axonal guidance and repulsion at the midline, as well as embryonic and postembryonic neuronal migrations. Interestingly, not all axons at the midline require catp-8/P5A-ATPase, although the axons run in the same fascicles and navigate the same space. Similarly, not all neuronal migrations require catp-8/P5A-ATPase. A CATP-8/P5A-ATPase reporter is localized to the ER in most, if not all, tissues and catp-8/P5A-ATPase can function both cell-autonomously and non-autonomously to regulate neuronal development. Genetic analyses establish that catp-8/P5A-ATPase can function in multiple pathways, including the Menorin pathway, previously shown to control dendritic patterning in PVD, and Wnt signaling, which functions to control neuronal migrations. Lastly, we show that catp-8/P5A-ATPase is required for localizing select transmembrane proteins necessary for dendrite morphogenesis. Collectively, our studies suggest that catp-8/P5A-ATPase serves diverse, yet specific, roles in different genetic pathways and may be involved in the regulation or localization of transmembrane and secreted proteins to specific subcellular compartments.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>34197450</pmid><doi>10.1371/journal.pgen.1009475</doi><orcidid>https://orcid.org/0000-0003-1795-0814</orcidid><orcidid>https://orcid.org/0000-0001-7946-2061</orcidid><orcidid>https://orcid.org/0000-0001-9631-0414</orcidid><orcidid>https://orcid.org/0000-0001-5853-3019</orcidid><orcidid>https://orcid.org/0000-0002-9465-2936</orcidid><orcidid>https://orcid.org/0000-0001-5922-9238</orcidid><orcidid>https://orcid.org/0000-0001-8264-8318</orcidid><orcidid>https://orcid.org/0000-0002-5943-8336</orcidid><orcidid>https://orcid.org/0000-0001-7394-860X</orcidid><orcidid>https://orcid.org/0000-0002-6271-0572</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine triphosphatase Amino acids Animals Axon guidance Axonogenesis Biology and Life Sciences Dendritic branching Embryos Genetic analysis Genetic aspects Genetic regulation Genetic research Genetic screening Genomes Homeostasis Lipids Localization Membrane proteins Membranes Morphogenesis Mutation Nervous system Neural circuitry Neurological research Neurons Pattern formation Physiological aspects Polyamines Proteins Research and Analysis Methods Wnt protein |
title | The CATP-8/P5A-type ATPase functions in multiple pathways during neuronal patterning |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T02%3A11%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20CATP-8/P5A-type%20ATPase%20functions%20in%20multiple%20pathways%20during%20neuronal%20patterning&rft.jtitle=PLoS%20genetics&rft.au=Tang,%20Leo%20T.%20H&rft.date=2021-07-01&rft.volume=17&rft.issue=7&rft.spage=e1009475&rft.epage=e1009475&rft.pages=e1009475-e1009475&rft.issn=1553-7404&rft.eissn=1553-7404&rft_id=info:doi/10.1371/journal.pgen.1009475&rft_dat=%3Cgale_plos_%3EA670983580%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2561940477&rft_id=info:pmid/34197450&rft_galeid=A670983580&rft_doaj_id=oai_doaj_org_article_540ad2045ac0405191519c82dd7f4017&rfr_iscdi=true |