PUBLICATION
Neuroendocrine transcriptional programs adapt dynamically to the supply and demand for neuropeptides as revealed in NSF mutant zebrafish
- Authors
- Kurrasch, D.M., Nevin, L.M., Wong, J., Baier, H., and Ingraham, H.A.
- ID
- ZDB-PUB-090629-25
- Date
- 2009
- Source
- Neural Development 4: 22 (Journal)
- Registered Authors
- Baier, Herwig, Kurrasch, Deborah, Nevin, Linda
- Keywords
- none
- MeSH Terms
-
- Animals
- Animals, Newborn
- Apoptosis/physiology
- Embryo, Nonmammalian
- Gene Expression Regulation, Developmental/genetics*
- Gonadotropin-Releasing Hormone/genetics
- Gonadotropin-Releasing Hormone/metabolism
- Hypothalamus*/cytology
- Hypothalamus*/embryology
- Hypothalamus*/growth & development
- In Situ Nick-End Labeling/methods
- Larva
- Mice
- Models, Biological
- Mutation/genetics*
- N-Ethylmaleimide-Sensitive Proteins/genetics
- N-Ethylmaleimide-Sensitive Proteins/metabolism*
- Neurons/metabolism*
- Neuropeptides/genetics
- Neuropeptides/metabolism*
- Oxytocin/genetics
- Oxytocin/metabolism
- Pro-Opiomelanocortin/metabolism
- Pyrrolidonecarboxylic Acid/analogs & derivatives
- Pyrrolidonecarboxylic Acid/metabolism
- Zebrafish/genetics
- Zebrafish/metabolism
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism*
- PubMed
- 19549326 Full text @ Neural Dev.
Citation
Kurrasch, D.M., Nevin, L.M., Wong, J., Baier, H., and Ingraham, H.A. (2009) Neuroendocrine transcriptional programs adapt dynamically to the supply and demand for neuropeptides as revealed in NSF mutant zebrafish. Neural Development. 4:22.
Abstract
BACKGROUND: Regulated secretion of specialized neuropeptides in the vertebrate neuroendocrine system is critical for ensuring physiological homeostasis. Expression of these cell-specific peptide markers in the differentiating hypothalamus commences prior to birth, often predating the physiological demand for secreted neuropeptides. The conserved function and spatial expression of hypothalamic peptides in vertebrates prompted us to search for critical neuroendocrine genes in newly hatched zebrafish larvae. RESULTS: We screened mutant 5-days-post-fertilization zebrafish larvae that fail to undergo visually mediated background adaptation for disruption in hypothalamic pomc expression. To our surprise, the ATPase N-ethylmaleimide sensitive factor (nsf) was identified as an essential gene for maintenance of neuroendocrine transcriptional programs during the embryo-to-larva transition. Despite normal hypothalamic development in nsfst53 mutants, neuropeptidergic cells exhibited a dramatic loss of cell-specific markers by 5 days post-fertilization that is accompanied by elevated intracellular neuropeptide protein. Consistent with the role of NSF in vesicle-membrane fusion events and intracellular trafficking, cytoplasmic endoplasmic reticulum-like membranes accumulate in nsf-/- hypothalamic neurons similar to that observed for SEC18 (nsf ortholog) yeast mutants. Our data support a model in which unspent neuropeptide cargo feedbacks to extinguish transcription in neuropeptidergic cells just as they become functionally required. In support of this model we found that gnrh3 transcripts remained unchanged in pre-migratory, non-functional gonadotropin-releasing hormone (GnRH) neurons in nsf-/- zebrafish. Furthermore, oxytocin-like (oxtl, intp) transcripts, which are found in osmoreceptive neurons and persist in mutant zebrafish, drop precipitously after nsf-/- zebrafish are acutely challenged with high salt. CONCLUSIONS: Our analyses of nsf mutant zebrafish reveal an unexpected role for NSF in hypothalamic development, with mutant 5-days-post-fertilization larvae exhibiting a stage-dependent loss of neuroendocrine transcripts and a corresponding accumulation of neuropeptides in the soma. Based on our collective findings, we speculate that neuroendocrine transcriptional programs adapt dynamically to both the supply and demand for neuropeptides to ensure adequate homeostatic responses.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping