Publication
Somatostatin signalling coordinates energy metabolism allocation to reproduction in zebrafish
| dc.contributor.author | Chen, Jie | |
| dc.contributor.author | Zhao, Wenting | |
| dc.contributor.author | Cao, Lei | |
| dc.contributor.author | Martins, Rute Sofia Tavares | |
| dc.contributor.author | Canario, Adelino | |
| dc.date.accessioned | 2024-09-28T10:07:17Z | |
| dc.date.available | 2024-09-28T10:07:17Z | |
| dc.date.issued | 2024-07-29 | |
| dc.description.abstract | BackgroundEnergy allocation between growth and reproduction determines puberty onset and fertility. In mammals, peripheral hormones such as leptin, insulin and ghrelin signal metabolic information to the higher centres controlling gonadotrophin-releasing hormone neurone activity. However, these observations could not be confirmed in lower vertebrates, suggesting that other factors may mediate the energetic trade-off between growth and reproduction. A bioinformatic and experimental study suggested co-regulation of the circadian clock, reproductive axis and growth-regulating genes in zebrafish. While loss-of-function of most of the identified co-regulated genes had no effect or only had mild effects on reproduction, no such information existed about the co-regulated somatostatin, well-known for its actions on growth and metabolism.ResultsWe show that somatostatin signalling is pivotal in regulating fecundity and metabolism. Knock-out of zebrafish somatostatin 1.1 (sst1.1) and somatostatin 1.2 (sst1.2) caused a 20-30% increase in embryonic primordial germ cells, and sst1.2-/- adults laid 40% more eggs than their wild-type siblings. The sst1.1-/- and sst1.2-/- mutants had divergent metabolic phenotypes: the former had 25% more pancreatic alpha-cells, were hyperglycaemic and glucose intolerant, and had increased adipocyte mass; the latter had 25% more pancreatic beta-cells, improved glucose clearance and reduced adipocyte mass.ConclusionsWe conclude that somatostatin signalling regulates energy metabolism and fecundity through anti-proliferative and modulatory actions on primordial germ cells, pancreatic insulin and glucagon cells and the hypothalamus. The ancient origin of the somatostatin system suggests it could act as a switch linking metabolism and reproduction across vertebrates. The results raise the possibility of applications in human and animal fertility. | eng |
| dc.identifier.doi | 10.1186/s12915-024-01961-7 | |
| dc.identifier.issn | 1741-7007 | |
| dc.identifier.uri | http://hdl.handle.net/10400.1/25961 | |
| dc.language.iso | eng | |
| dc.peerreviewed | yes | |
| dc.publisher | BioMed Central | |
| dc.relation | Algarve Centre for Marine Sciences | |
| dc.relation | Algarve Centre for Marine Sciences | |
| dc.relation | Centre for Marine and Environmental Research | |
| dc.relation | Somatostatin regulation of fecundity and potential application to sturgeon roe production | |
| dc.relation.ispartof | BMC Biology | |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
| dc.subject | Trade-offFecundity | |
| dc.subject | Metabolism | |
| dc.subject | Diabetes | |
| dc.subject | Zebrafish | |
| dc.subject | Pancreas | |
| dc.subject | Ovary | |
| dc.title | Somatostatin signalling coordinates energy metabolism allocation to reproduction in zebrafish | eng |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| oaire.awardTitle | Algarve Centre for Marine Sciences | |
| oaire.awardTitle | Algarve Centre for Marine Sciences | |
| oaire.awardTitle | Centre for Marine and Environmental Research | |
| oaire.awardTitle | Somatostatin regulation of fecundity and potential application to sturgeon roe production | |
| oaire.awardURI | info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04326%2F2020/PT | |
| oaire.awardURI | info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F04326%2F2020/PT | |
| oaire.awardURI | info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/LA%2FP%2F0101%2F2020/PT | |
| oaire.awardURI | http://hdl.handle.net/10400.1/25960 | |
| oaire.citation.issue | 1 | |
| oaire.citation.startPage | 163 | |
| oaire.citation.title | BMC Biology | |
| oaire.citation.volume | 22 | |
| oaire.fundingStream | 6817 - DCRRNI ID | |
| oaire.fundingStream | 6817 - DCRRNI ID | |
| oaire.fundingStream | 6817 - DCRRNI ID | |
| oaire.fundingStream | 3599-PPCDT | |
| oaire.version | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |
| person.familyName | Chen | |
| person.familyName | Martins | |
| person.familyName | Canario | |
| person.givenName | Jie | |
| person.givenName | Rute Sofia Tavares | |
| person.givenName | Adelino | |
| person.identifier | 143624 | |
| person.identifier.ciencia-id | 9210-A59A-9203 | |
| person.identifier.ciencia-id | A418-0899-1BD9 | |
| person.identifier.ciencia-id | 1F1E-D3B3-F804 | |
| person.identifier.orcid | 0000-0001-5804-2981 | |
| person.identifier.orcid | 0000-0002-6244-6468 | |
| person.identifier.rid | C-7942-2009 | |
| person.identifier.scopus-author-id | 56568523700 | |
| project.funder.identifier | http://doi.org/10.13039/501100001871 | |
| project.funder.identifier | http://doi.org/10.13039/501100001871 | |
| project.funder.identifier | http://doi.org/10.13039/501100001871 | |
| project.funder.name | Fundação para a Ciência e a Tecnologia | |
| project.funder.name | Fundação para a Ciência e a Tecnologia | |
| project.funder.name | Fundação para a Ciência e a Tecnologia | |
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