Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons

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 rev...

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Autor principal: Gelman, D.M
Otros Autores: Noaín, D., Avale, M.E, Otero, V., Low, M.J, Rubinstein, M.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2003
Acceso en línea:Registro en Scopus
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024 7 |2 scopus  |a 2-s2.0-0042386703 
024 7 |2 cas  |a dopamine, 51-61-6, 62-31-7; tyrosine 3 monooxygenase, 9036-22-0; Alkaline Phosphatase, EC 3.1.3.1; Catecholamines; Cre recombinase, EC 2.7.7.-; Integrases, EC 2.7.7.-; Tyrosine 3-Monooxygenase, EC 1.14.16.2; Viral Proteins 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a GNESF 
100 1 |a Gelman, D.M. 
245 1 0 |a Transgenic mice engineered to target Cre/LoxP-mediated DNA recombination into catecholaminergic neurons 
260 |c 2003 
270 1 0 |m Rubinstein, M.; INGEBI-CONICET, Vuelta de Obligado 2490, 1428-Buenos Aires, Argentina; email: mrubins@dna.uba.ar 
506 |2 openaire  |e Política editorial 
504 |a Asmus, S.E., Newman, S.W., Tyrosine hydroxylase mRNA-containing neurons in the medial amygdaloid nucleus and the reticular nucleus of the thalamus in the Syrian hamster (1993) Brain Res Mol Brain Res, 20, pp. 267-273 
504 |a Asmus, S.E., Kincaid, A.E., Newman, S.W., A species-specific population of tyrosine hydroxylase-immunoreactive neurons in the medial amygdaloid nucleus of the Syrian hamster (1992) Brain Res, 575, pp. 199-207 
504 |a Guillin, O., Diaz, J., Carroll, P., Griffon, N., Schwartz, J.C., Sokoloff, P., BDNF controls dopamine D3 receptor expression and triggers behavioural sensitization (2001) Nature, 411, pp. 86-89 
504 |a Gwinn-Hardy, K., Genetics of parkinsonism (2002) Mov Disord, 17, pp. 645-656 
504 |a Hillarp, N.A., Fuxe, K., Dahlstrom, A., Demonstration and mapping of central neurons containing dopamine, noradrenaline, and 5-hydroxytryptamine and their reactions to psychopharmaca (1966) Pharmacol Rev, 18, pp. 727-741 
504 |a Jonakait, G.M., Markey, K.A., Goldstein, M., Black, I.B., Transient expression of selected catecholaminergic traits in cranial sensory and dorsal root ganglia of the embryonic rat (1984) Dev Biol, 101, pp. 51-60 
504 |a Lobe, C.G., Koop, K.E., Kreppner, W., Lomeli, H., Gertsenstein, M., Nagy, A., Z/AP, a double reporter for cre-mediated recombination (1999) Dev Biol, 208, pp. 281-292 
504 |a Mezey, E., Phenylethanolamine N-methyltransferase-containing neurons in the limbic system of the young rat (1989) Proc Natl Acad Sci USA, 86, pp. 347-351 
504 |a Min, N., Joh, T.H., Kim, K.S., Peng, C., Son, J.H., 5′ upstream DNA sequence of the rat tyrosine hydroxylase gene directs high-level and tissue-specific expression to catecholaminergic neurons in the central nervous system of transgenic mice (1994) Brain Res Mol Brain Res, 27, pp. 281-289 
504 |a Mouradian, M.M., Recent advances in the genetics and pathogenesis of Parkinson disease (2002) Neurology, 5, pp. 179-185 
504 |a Nagy, A., Cre recombinase: The universal reagent for genome tailoring (2000) Genesis, 26, pp. 99-109 
504 |a Price, J., Mudge, A.W., A subpopulation of rat dorsal root ganglion neurons is catecholaminergic (1983) Nature, 301, pp. 241-243 
504 |a Rossant, J., McMahon, A., "Cre"-ating mouse mutants-a meeting review on conditional mouse genetics (1999) Genes Dev, 13, pp. 142-145 
504 |a Schimmel, J.J., Crews, L., Roffler-Tarlov, S., Chikaraishi, D.M., 4.5 kb of the rat tyrosine hydroxylase 5′ flanking sequence directs tissue specific expression during development and contains consensus sites for multiple transcription factors (1999) Brain Res Mol Brain Res, 74, pp. 1-14 
504 |a Zetterstrom, R.H., Solomin, L., Jansson, L., Hoffer, B.J., Olson, L., Perlmann, T., Dopamine neuron agenesis in Nurr1-deficient mice (1997) Science, 276, pp. 248-250 
520 3 |a 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. © 2003 Wiley-Liss, Inc.  |l eng 
593 |a Vollum Institute, Dept. of Behavioral Neuroscience, Oregon Health and Science University, Portland, OR, United States 
593 |a Centro de Estudios Cientificos, Valdivia, Chile 
593 |a INGEBI-CONICET, Vuelta de Obligado 2490, 1428-Buenos Aires, Argentina 
690 1 0 |a CATECHOLAMINE 
690 1 0 |a CRE RECOMBINASE 
690 1 0 |a DOPAMINE 
690 1 0 |a LOXP 
690 1 0 |a NOREPINEPHRINE 
690 1 0 |a TRANSGENIC MOUSE 
690 1 0 |a TYROSINE HYDROXYLASE 
690 1 0 |a CATECHOLAMINE 
690 1 0 |a CRE RECOMBINASE 
690 1 0 |a DOPAMINE 
690 1 0 |a GENE PRODUCT 
690 1 0 |a PROTEIN CRE LOXP 
690 1 0 |a RECOMBINANT DNA 
690 1 0 |a TYROSINE 3 MONOOXYGENASE 
690 1 0 |a UNCLASSIFIED DRUG 
690 1 0 |a ADRENAL MEDULLA 
690 1 0 |a ANIMAL CELL 
690 1 0 |a ARTICLE 
690 1 0 |a BRAIN REGION 
690 1 0 |a CATECHOLAMINE NERVE CELL 
690 1 0 |a CHROMAFFIN CELL 
690 1 0 |a DNA RECOMBINATION 
690 1 0 |a DOPAMINERGIC NERVE CELL 
690 1 0 |a DOUBLE IMMUNOHISTOCHEMISTRY 
690 1 0 |a FLOXED GENE 
690 1 0 |a GENE FUNCTION 
690 1 0 |a GENE MUTATION 
690 1 0 |a GENE TARGETING 
690 1 0 |a GENE TECHNOLOGY 
690 1 0 |a GENETIC ENGINEERING 
690 1 0 |a HYPOTHALAMUS 
690 1 0 |a IMMUNOFLUORESCENCE 
690 1 0 |a IMMUNOHISTOCHEMISTRY 
690 1 0 |a LOCUS CERULEUS 
690 1 0 |a MESENCEPHALON 
690 1 0 |a MOUSE 
690 1 0 |a NONHUMAN 
690 1 0 |a OLFACTORY BULB 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a PROMOTER REGION 
690 1 0 |a PROTEIN EXPRESSION 
690 1 0 |a PROTEIN LOCALIZATION 
690 1 0 |a RAT 
690 1 0 |a RETINA AMACRINE CELL 
690 1 0 |a STRAIN IDENTIFICATION 
690 1 0 |a SYMPATHETIC GANGLION 
690 1 0 |a TRANSGENIC MOUSE 
690 1 0 |a ALKALINE PHOSPHATASE 
690 1 0 |a ANIMALS 
690 1 0 |a BRAIN CHEMISTRY 
690 1 0 |a CATECHOLAMINES 
690 1 0 |a FEMALE 
690 1 0 |a GENE EXPRESSION REGULATION, ENZYMOLOGIC 
690 1 0 |a GENE TARGETING 
690 1 0 |a GENES, REPORTER 
690 1 0 |a GENETIC ENGINEERING 
690 1 0 |a HUMANS 
690 1 0 |a IMMUNOHISTOCHEMISTRY 
690 1 0 |a INTEGRASES 
690 1 0 |a MICE 
690 1 0 |a MICE, TRANSGENIC 
690 1 0 |a NEURONS 
690 1 0 |a PREGNANCY 
690 1 0 |a PROMOTER REGIONS (GENETICS) 
690 1 0 |a RATS 
690 1 0 |a RECOMBINATION, GENETIC 
690 1 0 |a TISSUE DISTRIBUTION 
690 1 0 |a TRANSGENES 
690 1 0 |a TYROSINE 3-MONOOXYGENASE 
690 1 0 |a VIRAL PROTEINS 
690 1 0 |a MUS MUSCULUS 
700 1 |a Noaín, D. 
700 1 |a Avale, M.E. 
700 1 |a Otero, V. 
700 1 |a Low, M.J. 
700 1 |a Rubinstein, M. 
773 0 |d 2003  |g v. 36  |h pp. 196-202  |k n. 4  |p Genesis  |x 1526954X  |t Genesis 
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856 4 0 |u https://hdl.handle.net/20.500.12110/paper_1526954X_v36_n4_p196_Gelman  |y Handle 
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