4.2 Article

Osmoregulation of the transcriptome of the hypothalamic supraoptic nucleus: A resource for the community

Journal

JOURNAL OF NEUROENDOCRINOLOGY
Volume 33, Issue 8, Pages -

Publisher

WILEY
DOI: 10.1111/jne.13007

Keywords

dehydration; plasticity; regulon; RNA sequencing; supraoptic nucleus; transcriptome

Funding

  1. Biotechnology and Biological Sciences Research Council [BB/J005452/1, BB/J015415/1, BB/R016879/1]
  2. Medical Research Council [MR/N022807/1, 1662603]
  3. The Leverhulme Trust [RPG-2017-287]
  4. British Heart Foundation [FS/17/60/33474]
  5. BBSRC [BB/J015415/1, BB/J005452/1, BB/R016879/1] Funding Source: UKRI
  6. MRC [MR/N022807/1] Funding Source: UKRI

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The hypothalamic supraoptic nucleus (SON) serves as a crucial osmoregulatory control center with different gene expression changes in euhydrated and dehydrated states, potentially involving regulatory networks and new research areas in neuroendocrinology.
The hypothalamic supraoptic nucleus (SON) is a core osmoregulatory control centre that deciphers information about the metabolic state of the organism and orchestrates appropriate homeostatic (endocrine) and allostatic (behavioural) responses. We have used RNA sequencing to describe the polyadenylated transcriptome of the SON of the male Wistar Han rat. These data have been mined to generate comprehensive catalogues of functional classes of genes (enzymes, transcription factors, endogenous peptides, G protein coupled receptors, transporters, catalytic receptors, channels and other pharmacological targets) expressed in this nucleus in the euhydrated state, and that together form the basal substrate for its physiological interactions. We have gone on to show that fluid deprivation for 3 days (dehydration) results in changes in the expression levels of 2247 RNA transcripts, which have similarly been functionally catalogued, and further mined to describe enriched gene categories and putative regulatory networks (Regulons) that may have physiological importance in SON function related plasticity. We hope that the revelation of these genes, pathways and networks, most of which have no characterised roles in the SON, will encourage the neuroendocrine community to pursue new investigations into the new 'known-unknowns' reported in the present study.

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