Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons
- Autores
- Gelman, Diego Matias; Noain, Daniela Maria Clara; Avale, Maria Elena; Otero Corchon, Veronica; Low, Malcolm J.; Rubinstein, Marcelo
- Año de publicación
- 2003
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- To introduce restricted DNA recombination events into catecholaminergic neurons using the Cre/loxP technology, we generated transgenic mice carrying the Cre recombinase gene driven by a 9 kb rat tyrosine hydroxylase (TH) promoter. Immunohistochemistry performed on transgenic mouse brain sections revealed a high number of cells expressing Cre in areas where TH is normally expressed, including the olfactory bulb, hypothalamic and midbrain dopaminergic neurons, and the locus coeruleus. Double immunohistochemistry and immunofluorescence indicated that colocalization of TH and Cre is greater than 80%. Cre expression was also found in TH-positive amacrine neurons of the retina, chromaffin cells of the adrenal medulla, and sympathetic ganglia. We intercrossed TH-Cre mice with the floxed reporter strain Z/AP and observed efficient Cre-mediated recombination in all areas expressing TH, indicating that transgenic Cre is functional. Therefore, we have generated a valuable transgenic mouse strain to induce specific mutations of "floxed" genes in catecholaminergic neurons.
Fil: Gelman, Diego Matias. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Noain, Daniela Maria Clara. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Avale, Maria Elena. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Otero Corchon, Veronica. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Low, Malcolm J.. Oregon Health and Science University; Estados Unidos
Fil: Rubinstein, Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina. Centro de Estudios Científicos; Chile - Materia
-
Catecholamine
Cre Recombinase
Dopamine
Loxp
Norepinephrine
Transgenic Mouse
Tyrosine Hydroxylase - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/79707
Ver los metadatos del registro completo
id |
CONICETDig_b783a90def3911cee9c75dcfc5a28682 |
---|---|
oai_identifier_str |
oai:ri.conicet.gov.ar:11336/79707 |
network_acronym_str |
CONICETDig |
repository_id_str |
3498 |
network_name_str |
CONICET Digital (CONICET) |
spelling |
Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neuronsGelman, Diego MatiasNoain, Daniela Maria ClaraAvale, Maria ElenaOtero Corchon, VeronicaLow, Malcolm J.Rubinstein, MarceloCatecholamineCre RecombinaseDopamineLoxpNorepinephrineTransgenic MouseTyrosine Hydroxylasehttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1To introduce restricted DNA recombination events into catecholaminergic neurons using the Cre/loxP technology, we generated transgenic mice carrying the Cre recombinase gene driven by a 9 kb rat tyrosine hydroxylase (TH) promoter. Immunohistochemistry performed on transgenic mouse brain sections revealed a high number of cells expressing Cre in areas where TH is normally expressed, including the olfactory bulb, hypothalamic and midbrain dopaminergic neurons, and the locus coeruleus. Double immunohistochemistry and immunofluorescence indicated that colocalization of TH and Cre is greater than 80%. Cre expression was also found in TH-positive amacrine neurons of the retina, chromaffin cells of the adrenal medulla, and sympathetic ganglia. We intercrossed TH-Cre mice with the floxed reporter strain Z/AP and observed efficient Cre-mediated recombination in all areas expressing TH, indicating that transgenic Cre is functional. Therefore, we have generated a valuable transgenic mouse strain to induce specific mutations of "floxed" genes in catecholaminergic neurons.Fil: Gelman, Diego Matias. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Noain, Daniela Maria Clara. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Avale, Maria Elena. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Otero Corchon, Veronica. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Low, Malcolm J.. Oregon Health and Science University; Estados UnidosFil: Rubinstein, Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina. Centro de Estudios Científicos; ChileWiley-liss, Div John Wiley & Sons Inc2003-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/79707Gelman, Diego Matias; Noain, Daniela Maria Clara; Avale, Maria Elena; Otero Corchon, Veronica; Low, Malcolm J.; et al.; Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons; Wiley-liss, Div John Wiley & Sons Inc; Genesis; 36; 4; 8-2003; 196-2021526-954XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pubmed/12929090info:eu-repo/semantics/altIdentifier/doi/10.1002/gene.10217info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/gene.10217info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:35:16Zoai:ri.conicet.gov.ar:11336/79707instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 09:35:16.398CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons |
title |
Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons |
spellingShingle |
Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons Gelman, Diego Matias Catecholamine Cre Recombinase Dopamine Loxp Norepinephrine Transgenic Mouse Tyrosine Hydroxylase |
title_short |
Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons |
title_full |
Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons |
title_fullStr |
Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons |
title_full_unstemmed |
Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons |
title_sort |
Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons |
dc.creator.none.fl_str_mv |
Gelman, Diego Matias Noain, Daniela Maria Clara Avale, Maria Elena Otero Corchon, Veronica Low, Malcolm J. Rubinstein, Marcelo |
author |
Gelman, Diego Matias |
author_facet |
Gelman, Diego Matias Noain, Daniela Maria Clara Avale, Maria Elena Otero Corchon, Veronica Low, Malcolm J. Rubinstein, Marcelo |
author_role |
author |
author2 |
Noain, Daniela Maria Clara Avale, Maria Elena Otero Corchon, Veronica Low, Malcolm J. Rubinstein, Marcelo |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
Catecholamine Cre Recombinase Dopamine Loxp Norepinephrine Transgenic Mouse Tyrosine Hydroxylase |
topic |
Catecholamine Cre Recombinase Dopamine Loxp Norepinephrine Transgenic Mouse Tyrosine Hydroxylase |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
To introduce restricted DNA recombination events into catecholaminergic neurons using the Cre/loxP technology, we generated transgenic mice carrying the Cre recombinase gene driven by a 9 kb rat tyrosine hydroxylase (TH) promoter. Immunohistochemistry performed on transgenic mouse brain sections revealed a high number of cells expressing Cre in areas where TH is normally expressed, including the olfactory bulb, hypothalamic and midbrain dopaminergic neurons, and the locus coeruleus. Double immunohistochemistry and immunofluorescence indicated that colocalization of TH and Cre is greater than 80%. Cre expression was also found in TH-positive amacrine neurons of the retina, chromaffin cells of the adrenal medulla, and sympathetic ganglia. We intercrossed TH-Cre mice with the floxed reporter strain Z/AP and observed efficient Cre-mediated recombination in all areas expressing TH, indicating that transgenic Cre is functional. Therefore, we have generated a valuable transgenic mouse strain to induce specific mutations of "floxed" genes in catecholaminergic neurons. Fil: Gelman, Diego Matias. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina Fil: Noain, Daniela Maria Clara. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina Fil: Avale, Maria Elena. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina Fil: Otero Corchon, Veronica. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina Fil: Low, Malcolm J.. Oregon Health and Science University; Estados Unidos Fil: Rubinstein, Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina. Centro de Estudios Científicos; Chile |
description |
To introduce restricted DNA recombination events into catecholaminergic neurons using the Cre/loxP technology, we generated transgenic mice carrying the Cre recombinase gene driven by a 9 kb rat tyrosine hydroxylase (TH) promoter. Immunohistochemistry performed on transgenic mouse brain sections revealed a high number of cells expressing Cre in areas where TH is normally expressed, including the olfactory bulb, hypothalamic and midbrain dopaminergic neurons, and the locus coeruleus. Double immunohistochemistry and immunofluorescence indicated that colocalization of TH and Cre is greater than 80%. Cre expression was also found in TH-positive amacrine neurons of the retina, chromaffin cells of the adrenal medulla, and sympathetic ganglia. We intercrossed TH-Cre mice with the floxed reporter strain Z/AP and observed efficient Cre-mediated recombination in all areas expressing TH, indicating that transgenic Cre is functional. Therefore, we have generated a valuable transgenic mouse strain to induce specific mutations of "floxed" genes in catecholaminergic neurons. |
publishDate |
2003 |
dc.date.none.fl_str_mv |
2003-08 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/79707 Gelman, Diego Matias; Noain, Daniela Maria Clara; Avale, Maria Elena; Otero Corchon, Veronica; Low, Malcolm J.; et al.; Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons; Wiley-liss, Div John Wiley & Sons Inc; Genesis; 36; 4; 8-2003; 196-202 1526-954X CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/79707 |
identifier_str_mv |
Gelman, Diego Matias; Noain, Daniela Maria Clara; Avale, Maria Elena; Otero Corchon, Veronica; Low, Malcolm J.; et al.; Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons; Wiley-liss, Div John Wiley & Sons Inc; Genesis; 36; 4; 8-2003; 196-202 1526-954X CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pubmed/12929090 info:eu-repo/semantics/altIdentifier/doi/10.1002/gene.10217 info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/gene.10217 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Wiley-liss, Div John Wiley & Sons Inc |
publisher.none.fl_str_mv |
Wiley-liss, Div John Wiley & Sons Inc |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
_version_ |
1844613097214443520 |
score |
13.070432 |