Cell-type specific oxytocin gene expression from AAV delivered promoter deletion constructs into the rat supraoptic nucleus in vivo.

The magnocellular neurons (MCNs) in the hypothalamus selectively express either oxytocin (OXT) or vasopressin (AVP) neuropeptide genes, a property that defines their phenotypes. Here we examine the molecular basis of this selectivity in the OXT MCNs by stereotaxic microinjections of adeno-associated...

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Autores principales: Raymond L Fields, Todd A Ponzio, Makoto Kawasaki, Harold Gainer
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Publicado: Public Library of Science (PLoS) 2012
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Acceso en línea:https://doaj.org/article/007a3c0d7667495c99002bf301bddbd0
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spelling oai:doaj.org-article:007a3c0d7667495c99002bf301bddbd02021-11-18T07:27:12ZCell-type specific oxytocin gene expression from AAV delivered promoter deletion constructs into the rat supraoptic nucleus in vivo.1932-620310.1371/journal.pone.0032085https://doaj.org/article/007a3c0d7667495c99002bf301bddbd02012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22363799/?tool=EBIhttps://doaj.org/toc/1932-6203The magnocellular neurons (MCNs) in the hypothalamus selectively express either oxytocin (OXT) or vasopressin (AVP) neuropeptide genes, a property that defines their phenotypes. Here we examine the molecular basis of this selectivity in the OXT MCNs by stereotaxic microinjections of adeno-associated virus (AAV) vectors that contain various OXT gene promoter deletion constructs using EGFP as the reporter into the rat supraoptic nucleus (SON). Two weeks following injection of the AAVs, immunohistochemical assays of EGFP expression from these constructs were done to determine whether the EGFP reporter co-localizes with either the OXT- or AVP-immunoreactivity in the MCNs. The results show that the key elements in the OT gene promoter that regulate the cell-type specific expression the SON are located -216 to -100 bp upstream of the transcription start site. We hypothesize that within this 116 bp domain a repressor exists that inhibits expression specifically in AVP MCNs, thereby leading to the cell-type specific expression of the OXT gene only in the OXT MCNs.Raymond L FieldsTodd A PonzioMakoto KawasakiHarold GainerPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 2, p e32085 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Raymond L Fields
Todd A Ponzio
Makoto Kawasaki
Harold Gainer
Cell-type specific oxytocin gene expression from AAV delivered promoter deletion constructs into the rat supraoptic nucleus in vivo.
description The magnocellular neurons (MCNs) in the hypothalamus selectively express either oxytocin (OXT) or vasopressin (AVP) neuropeptide genes, a property that defines their phenotypes. Here we examine the molecular basis of this selectivity in the OXT MCNs by stereotaxic microinjections of adeno-associated virus (AAV) vectors that contain various OXT gene promoter deletion constructs using EGFP as the reporter into the rat supraoptic nucleus (SON). Two weeks following injection of the AAVs, immunohistochemical assays of EGFP expression from these constructs were done to determine whether the EGFP reporter co-localizes with either the OXT- or AVP-immunoreactivity in the MCNs. The results show that the key elements in the OT gene promoter that regulate the cell-type specific expression the SON are located -216 to -100 bp upstream of the transcription start site. We hypothesize that within this 116 bp domain a repressor exists that inhibits expression specifically in AVP MCNs, thereby leading to the cell-type specific expression of the OXT gene only in the OXT MCNs.
format article
author Raymond L Fields
Todd A Ponzio
Makoto Kawasaki
Harold Gainer
author_facet Raymond L Fields
Todd A Ponzio
Makoto Kawasaki
Harold Gainer
author_sort Raymond L Fields
title Cell-type specific oxytocin gene expression from AAV delivered promoter deletion constructs into the rat supraoptic nucleus in vivo.
title_short Cell-type specific oxytocin gene expression from AAV delivered promoter deletion constructs into the rat supraoptic nucleus in vivo.
title_full Cell-type specific oxytocin gene expression from AAV delivered promoter deletion constructs into the rat supraoptic nucleus in vivo.
title_fullStr Cell-type specific oxytocin gene expression from AAV delivered promoter deletion constructs into the rat supraoptic nucleus in vivo.
title_full_unstemmed Cell-type specific oxytocin gene expression from AAV delivered promoter deletion constructs into the rat supraoptic nucleus in vivo.
title_sort cell-type specific oxytocin gene expression from aav delivered promoter deletion constructs into the rat supraoptic nucleus in vivo.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/007a3c0d7667495c99002bf301bddbd0
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AT makotokawasaki celltypespecificoxytocingeneexpressionfromaavdeliveredpromoterdeletionconstructsintotheratsupraopticnucleusinvivo
AT haroldgainer celltypespecificoxytocingeneexpressionfromaavdeliveredpromoterdeletionconstructsintotheratsupraopticnucleusinvivo
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