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Authordc.contributor.authorTeraoka, H. 
Authordc.contributor.authorRussell, C. es_CL
Authordc.contributor.authorRegan, J. es_CL
Authordc.contributor.authorChandrasekhar, A. es_CL
Authordc.contributor.authorConcha, Miguel L. es_CL
Authordc.contributor.authorYokoyama, R. es_CL
Authordc.contributor.authorHigashi, K. es_CL
Authordc.contributor.authorTake-uchi, M. es_CL
Authordc.contributor.authorDong, W. es_CL
Authordc.contributor.authorHiraga, T. es_CL
Authordc.contributor.authorHolder, N. es_CL
Authordc.contributor.authorWilson, S. W. es_CL
Admission datedc.date.accessioned2007-05-07T20:25:07Z
Available datedc.date.available2007-05-07T20:25:07Z
Publication datedc.date.issued2004-09-05
Cita de ítemdc.identifier.citationJOURNAL OF NEUROBIOLOGY 60 (3): 275-288 SEP 5 2004en
Identifierdc.identifier.issn0022-3034
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/127135
Abstractdc.description.abstractSerotonin (5HT) plays major roles in the physiological regulation of many behavioral processes, including sleep, feeding, and mood, but the genetic mechanisms by which serotonergic neurons arise during development are poorly understood. In the present study, we have investigated the development of serotonergic neurons in the zebratish. Neurons exhibiting 5HT-immunoreactivity (5HT-IR) are detected from 45 h postfertilization (hpf) in the ventral hindbrain raphe, the hypothalamus, pineal organ, and pretectal area. Tryptophan hydroxylases encode rate-limiting enzymes that function in the synthesis of 5HT. As part of this study, we cloned and analyzed a novel zebralish tph gene. named tphR. Unlike two other zebrafish tph genes QphD1 and tphD2), tphR is expressed in serotonergic raphe neurons, similar to tph genes in mammalian species. tphR is also expressed in the pineal organ where it is likely to be involved in the pathway leading to synthesis of melatonin. To better understand the signaling pathways involved in the induction of the serotonergic phenotype, we analyzed tphR expression and 5HT-IR in embryos in which either Hh or Fgf signals are abrogated. Hindbrain 511T neurons are severely reduced in mutants lacking activity of either Ace/Fgf8 or the transcription factor Noi/Pax2.1, which regulates expression of ace/fgf8, and probably other genes encoding signaling proteins. Similarly, serotonergic raphe neurons are absent in embryos lacking Hh activity confirming a conserved role for Hh signals in the induction of these cells. Conversely, over-activation of the Hh pathway increases the number of serotonergic neurons. As in mammals, our results are consistent with the transcription factors Nk2.2 and Gata3 acting downstream of Hh activity in the development of serotonergic raphe neurons. Our results show that the pathways involved in induction of hindbrain serotonergic neurons are likely to be conserved in all vertebrates and help establish the zebrafish as a model system to study this important neuronal class.en
Lenguagedc.language.isoenen
Publisherdc.publisherJOHN WILEY & SONSen
Keywordsdc.subjectENCODING TRYPTOPHAN-HYDROXYLASEen
Títulodc.titleHedgehog and Fgf signaling pathways regulate the development of tphR-expressing serotonergic raphe neurons in zebrafish embryosen
Document typedc.typeArtículo de revista


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