Estimates of recent and historical effective population size in turbot, seabream, seabass and carp selective breeding programmes.


Journal

Genetics, selection, evolution : GSE
ISSN: 1297-9686
Titre abrégé: Genet Sel Evol
Pays: France
ID NLM: 9114088

Informations de publication

Date de publication:
06 Nov 2021
Historique:
received: 01 02 2021
accepted: 22 10 2021
entrez: 7 11 2021
pubmed: 8 11 2021
medline: 26 11 2021
Statut: epublish

Résumé

The high fecundity of fish species allows intense selection to be practised and therefore leads to fast genetic gains. Based on this, numerous selective breeding programmes have been started in Europe in the last decades, but in general, little is known about how the base populations of breeders have been built. Such knowledge is important because base populations can be created from very few individuals, which can lead to small effective population sizes and associated reductions in genetic variability. In this study, we used genomic information that was recently made available for turbot (Scophthalmus maximus), gilthead seabream (Sparus aurata), European seabass (Dicentrarchus labrax) and common carp (Cyprinus carpio) to obtain accurate estimates of the effective size for commercial populations. Restriction-site associated DNA sequencing data were used to estimate current and historical effective population sizes. We used a novel method that considers the linkage disequilibrium spectrum for the whole range of genetic distances between all pairs of single nucleotide polymorphisms (SNPs), and thus accounts for potential fluctuations in population size over time. Our results show that the current effective population size for these populations is small (equal to or less than 50 fish), potentially putting the sustainability of the breeding programmes at risk. We have also detected important drops in effective population size about five to nine generations ago, most likely as a result of domestication and the start of selective breeding programmes for these species in Europe. Our findings highlight the need to broaden the genetic composition of the base populations from which selection programmes start, and suggest that measures designed to increase effective population size within all farmed populations analysed here should be implemented in order to manage genetic variability and ensure the sustainability of the breeding programmes.

Sections du résumé

BACKGROUND BACKGROUND
The high fecundity of fish species allows intense selection to be practised and therefore leads to fast genetic gains. Based on this, numerous selective breeding programmes have been started in Europe in the last decades, but in general, little is known about how the base populations of breeders have been built. Such knowledge is important because base populations can be created from very few individuals, which can lead to small effective population sizes and associated reductions in genetic variability. In this study, we used genomic information that was recently made available for turbot (Scophthalmus maximus), gilthead seabream (Sparus aurata), European seabass (Dicentrarchus labrax) and common carp (Cyprinus carpio) to obtain accurate estimates of the effective size for commercial populations.
METHODS METHODS
Restriction-site associated DNA sequencing data were used to estimate current and historical effective population sizes. We used a novel method that considers the linkage disequilibrium spectrum for the whole range of genetic distances between all pairs of single nucleotide polymorphisms (SNPs), and thus accounts for potential fluctuations in population size over time.
RESULTS RESULTS
Our results show that the current effective population size for these populations is small (equal to or less than 50 fish), potentially putting the sustainability of the breeding programmes at risk. We have also detected important drops in effective population size about five to nine generations ago, most likely as a result of domestication and the start of selective breeding programmes for these species in Europe.
CONCLUSIONS CONCLUSIONS
Our findings highlight the need to broaden the genetic composition of the base populations from which selection programmes start, and suggest that measures designed to increase effective population size within all farmed populations analysed here should be implemented in order to manage genetic variability and ensure the sustainability of the breeding programmes.

Identifiants

pubmed: 34742227
doi: 10.1186/s12711-021-00680-9
pii: 10.1186/s12711-021-00680-9
pmc: PMC8572424
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

85

Subventions

Organisme : Seventh Framework Programme
ID : KBBE.2013.1.2-659 10 under grant agreement n° 613611 FISHBOOST project
Organisme : Horizon 2020
ID : 727315 MedAID project
Organisme : Ministerio de Ciencia e Innovación (ES)
ID : CGL2016-75904-C2
Organisme : Xunta de Galicia (ES)
ID : ED431C 2020-05
Organisme : Ministry of Education, Youth and Sports (CZ)
ID : Project Biodiverzity (CZ.02.1.01/0.0/0.0/16_025/0007370)
Organisme : MCIN/ AEI /10.13039/501100011033
ID : PID2020-114426GB-C22
Organisme : MCIN/ AEI /10.13039/501100011033
ID : PID2020-114426GB-C2

Informations de copyright

© 2021. The Author(s).

Références

Nat Rev Genet. 2011 Sep 16;12(10):703-14
pubmed: 21921926
Genet Sel Evol. 2019 Jun 6;51(1):26
pubmed: 31170906
Anim Genet. 2017 Apr;48(2):237-241
pubmed: 27699807
Theor Appl Genet. 1968 Jun;38(6):226-31
pubmed: 24442307
J Biomed Biotechnol. 2011;2011:329025
pubmed: 21049003
Front Genet. 2019 Sep 04;10:745
pubmed: 31552083
Genetics. 2014 Jun;197(2):769-80
pubmed: 24717176
Nat Genet. 2014 Nov;46(11):1212-9
pubmed: 25240282
J Anim Sci. 1997 Apr;75(4):934-40
pubmed: 9110204
Evol Appl. 2018 Apr 06;11(8):1322-1341
pubmed: 30151043
Mol Biol Evol. 2020 Dec 16;37(12):3642-3653
pubmed: 32642779
Mol Biol Evol. 2019 Mar 1;36(3):632-637
pubmed: 30517680
Genetics. 2011 Oct;189(2):633-44
pubmed: 21840864
Genome Res. 2003 Apr;13(4):635-43
pubmed: 12654718
DNA Res. 2018 Aug 1;25(4):439-450
pubmed: 29897548
BMC Genet. 2012 Jul 02;13:54
pubmed: 22747677
Heredity (Edinb). 2017 Feb;118(2):177-185
pubmed: 27624114
Anim Genet. 2008 Dec;39(6):623-34
pubmed: 18828863
BMC Genomics. 2015 Nov 11;16:922
pubmed: 26559809
Genet Sel Evol. 2018 Jun 8;50(1):30
pubmed: 29884113
Genet Sel Evol. 2016 Jun 24;48(1):46
pubmed: 27342705
Front Genet. 2018 Dec 14;9:649
pubmed: 30619473
BMC Genet. 2018 Jul 11;19(1):43
pubmed: 29996763
Front Genet. 2019 May 22;10:498
pubmed: 31191613
Front Genet. 2014 Nov 25;5:414
pubmed: 25505485
G3 (Bethesda). 2018 Nov 6;8(11):3507-3513
pubmed: 30150301

Auteurs

María Saura (M)

Departamento de Mejora Genética Animal, INIA-CSIC, Ctra. de La Coruña, km 7.5, 28040, Madrid, Spain. saura.maria@inia.es.

Armando Caballero (A)

Centro de Investigación Mariña, Facultade de Bioloxía, Universidade de Vigo, 36310, Vigo, Spain.

Enrique Santiago (E)

Departamento de Biología Funcional, Universidad de Oviedo, C/ Julián Clavería s/n, 33006, Oviedo, Spain.

Almudena Fernández (A)

Departamento de Mejora Genética Animal, INIA-CSIC, Ctra. de La Coruña, km 7.5, 28040, Madrid, Spain.

Elisabeth Morales-González (E)

Departamento de Mejora Genética Animal, INIA-CSIC, Ctra. de La Coruña, km 7.5, 28040, Madrid, Spain.

Jesús Fernández (J)

Departamento de Mejora Genética Animal, INIA-CSIC, Ctra. de La Coruña, km 7.5, 28040, Madrid, Spain.

Santiago Cabaleiro (S)

CETGA, Cluster de Acuicultura de Galicia, Punta do Couso s/n, 15695, Aguiño-Ribeira, Spain.

Adrián Millán (A)

Geneaqua, 27002, Lugo, Spain.

Paulino Martínez (P)

Departament of Zoology, Genetics and Physical Anthropology, Universidade de Santiago de Compostela, 27002, Lugo, Spain.

Christos Palaiokostas (C)

The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Midlothian, EH25 9RG, UK.

Martin Kocour (M)

South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, Faculty of Fisheries and Protection of Waters, University of South Bohemia in České Budějovice, Zátiší 728/II, 389 25, Vodňany, Czech Republic.

Muhammad L Aslam (ML)

Nofima AS, P.O. Box 210, 1431, Ås, Norway.

Ross D Houston (RD)

The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Midlothian, EH25 9RG, UK.

Martin Prchal (M)

South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, Faculty of Fisheries and Protection of Waters, University of South Bohemia in České Budějovice, Zátiší 728/II, 389 25, Vodňany, Czech Republic.

Luca Bargelloni (L)

Universitá degli Studi di Padova, Via 8 Febbraio 1848, 2, 35122, Padova, PD, Italy.

Kostas Tzokas (K)

Andromeda Group SA, Leof. Lavriou 99, 190 02, Peania, Greece.

Pierrick Haffray (P)

SYSAAF, Station LPGP/INRAE, Campus de Beaulieu, 35042, Rennes, France.

Jean-Sebastien Bruant (JS)

Ferme Marine De Douhet, Route du Douhet, 17840, La Brée-les-Bains, France.

Beatriz Villanueva (B)

Departamento de Mejora Genética Animal, INIA-CSIC, Ctra. de La Coruña, km 7.5, 28040, Madrid, Spain.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH