<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>51</viewCount><searchCount>0</searchCount></scores><additional><submitter>Politano SF</submitter><funding>ODCDC CDC HHS</funding><funding>NINDS NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><pagination>335-349</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6848449</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>79(4)</volume><pubmed_abstract>The coordinated growth and development of synapses is critical for all aspects of neural circuit function and mutations that disrupt these processes can result in various neurological defects. Several anterograde and retrograde signaling pathways, including the canonical Bone Morphogenic Protein (BMP) pathway, regulate synaptic development in vertebrates and invertebrates. At the Drosophila larval neuromuscular junction (NMJ), the retrograde BMP pathway is a part of the machinery that controls NMJ expansion concurrent with larval growth. We sought to determine whether the conserved Hippo pathway, critical for proportional growth in other tissues, also functions in NMJ development. We found that neuronal loss of the serine-threonine protein kinase Tao, a regulator of the Hippo signaling pathway, results in supernumerary boutons which contain a normal density of active zones. Tao is also required for proper synaptic function, as reduction of Tao results in NMJs with decreased evoked excitatory junctional potentials. Surprisingly, Tao function in NMJ growth is independent of the Hippo pathway. Instead, our experiments suggest that Tao negatively regulates BMP signaling as reduction of Tao leads to an increase in pMad levels in motor neuron nuclei and an increase in BMP target gene expression. Taken together, these results support a role for Tao as a novel inhibitor of BMP signaling in motor neurons during synaptic development and function.</pubmed_abstract><journal>Developmental neurobiology</journal><pubmed_title>Tao Negatively Regulates BMP Signaling During Neuromuscular Junction Development in Drosophila.</pubmed_title><pmcid>PMC6848449</pmcid><funding_grant_id>K01 NS102342</funding_grant_id><funding_grant_id>K01NS102342</funding_grant_id><funding_grant_id>R01 GM084947</funding_grant_id><funding_grant_id>P40 OD018537</funding_grant_id><pubmed_authors>Salemme RR</pubmed_authors><pubmed_authors>Juszczak MJ</pubmed_authors><pubmed_authors>Quinn JP</pubmed_authors><pubmed_authors>Phillip LK</pubmed_authors><pubmed_authors>Vanderzalm PJ</pubmed_authors><pubmed_authors>Ashley J</pubmed_authors><pubmed_authors>Carrillo RA</pubmed_authors><pubmed_authors>Lopez-Rivera JA</pubmed_authors><pubmed_authors>Bakula TA</pubmed_authors><pubmed_authors>Puhalla KA</pubmed_authors><pubmed_authors>Politano SF</pubmed_authors><view_count>51</view_count></additional><is_claimable>false</is_claimable><name>Tao Negatively Regulates BMP Signaling During Neuromuscular Junction Development in Drosophila.</name><description>The coordinated growth and development of synapses is critical for all aspects of neural circuit function and mutations that disrupt these processes can result in various neurological defects. Several anterograde and retrograde signaling pathways, including the canonical Bone Morphogenic Protein (BMP) pathway, regulate synaptic development in vertebrates and invertebrates. At the Drosophila larval neuromuscular junction (NMJ), the retrograde BMP pathway is a part of the machinery that controls NMJ expansion concurrent with larval growth. We sought to determine whether the conserved Hippo pathway, critical for proportional growth in other tissues, also functions in NMJ development. We found that neuronal loss of the serine-threonine protein kinase Tao, a regulator of the Hippo signaling pathway, results in supernumerary boutons which contain a normal density of active zones. Tao is also required for proper synaptic function, as reduction of Tao results in NMJs with decreased evoked excitatory junctional potentials. Surprisingly, Tao function in NMJ growth is independent of the Hippo pathway. Instead, our experiments suggest that Tao negatively regulates BMP signaling as reduction of Tao leads to an increase in pMad levels in motor neuron nuclei and an increase in BMP target gene expression. Taken together, these results support a role for Tao as a novel inhibitor of BMP signaling in motor neurons during synaptic development and function.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Apr</publication><modification>2024-12-03T21:13:21.251Z</modification><creation>2020-10-30T08:15:58Z</creation></dates><accession>S-EPMC6848449</accession><cross_references><pubmed>31002474</pubmed><doi>10.1002/dneu.22681</doi></cross_references></HashMap>