• Aucun résultat trouvé

How to use molecular data to account for non random mating in quantitative genetic estimates derived from family structured experiments

N/A
N/A
Protected

Academic year: 2021

Partager "How to use molecular data to account for non random mating in quantitative genetic estimates derived from family structured experiments"

Copied!
3
0
0

Texte intégral

(1)

HAL Id: hal-01269078

https://hal.archives-ouvertes.fr/hal-01269078

Submitted on 5 Jun 2020

HAL is a multi-disciplinary open access archive for the deposit and dissemination of sci-entific research documents, whether they are pub-lished or not. The documents may come from teaching and research institutions in France or abroad, or from public or private research centers.

L’archive ouverte pluridisciplinaire HAL, est destinée au dépôt et à la diffusion de documents scientifiques de niveau recherche, publiés ou non, émanant des établissements d’enseignement et de recherche français ou étrangers, des laboratoires publics ou privés.

How to use molecular data to account for non random

mating in quantitative genetic estimates derived from

family structured experiments

Sylvie Muratorio, Laurène Gay, Etienne Klein

To cite this version:

Sylvie Muratorio, Laurène Gay, Etienne Klein. How to use molecular data to account for non random mating in quantitative genetic estimates derived from family structured experiments. 4. International Statistical Ecology Conference (ISEC 2014), Jul 2014, Montpellier, France. 1 p. �hal-01269078�

(2)

4th International Statistical Ecology Conference

Montpellier, France

1-4 July 2014

(3)

How to use molecular data to account for non random mating in quantitative genetic estimates derived from family structured experiments

Julie GAÜZEREa, Sylvie ODDOU-MURATORIOa, Laurène GAYb and Etienne KLEINc

a UR629 Ecologie des Forêts Méditerranéennes (URFM), F-84914 Avignon, France b UMR 1334 Amélioration génétique et adaptation des plantes méditerranéennes et tropicales

(AGAP), F-34060 Montpellier, France

c UR546 Biostatistiques et Processus Spatiaux (BioSP), F-84914 Avignon, France

Keywords: evolutionary ecology, survey design and analysis, quantitative genetics, pedigree-free methods

Abstract: Accurate estimates of heritability (h²) of fitness-related traits are necessary to assess their

adaptive response in changing environments. For plants, maternal families are often sampled to estimate h². Estimates thus rely on several assumptions about the mating system and the relatedness among mates (basically offspring are assumed to be half-sibs or unrelated). In particular, when mating events are impossible to observe and sample sizes are large, the paternal relatedness is often neglected, leading to bias in the h² estimates.

We performed a simulation study to investigate how molecular markers can be used to analyze more efficiently the family structured designs. We compared the simple method based on a maternal family model assumption with methods using marker-based relatedness coefficients, pedigree or hybrid genetic information (animal models) to account for paternal relatedness. We assessed the effect of unequal male reproductive success, inbreeding and maternal effects on h² estimates.

Results showed that in presence of unequal male reproductive success, neglecting the genetic relatedness between families led to bias the h² estimates derived from the family model. Regarding the animal model, the method using mean marker-based relatedness coefficients was efficient to deal with non-random mating system and ancestral inbreeding in the parental population. But this method was biased in presence of maternal effects. In such cases, only the use of finest genetic information, like pedigrees, allowed to improve the accuracy of the h² estimates. Using a hybrid approach, that uses both the pedigree and mean relatedness information, was efficient to deal with any departures from the family assumptions.

In conclusion, family structure designs are part of the experimental exceptions, with inbred samples, where pedigree-free, or partial pedigree-free (also called hybrid approach), methods can be used to get accurate h² estimates, at the condition that mean relatedness coefficients are used (estimated at the family/population level).

Références

Documents relatifs

The first patient died few hours after birth by hydrops fetalis, the second one presented with neonatal jaundice and severe anemia necessitating urgent blood transfusion.. This

Hevea brasiliensis ; breeding ; latex production ; metabolic typology of rubber clones ; latex diagnostic ; molecular genetic markers ; microsatellites ; genetic linkage mapping

Pour les infections urinaires chez cette population, le traitement choisi devrait idéalement être le plus spéci- fique possible afin de limiter l’émergence de résistances et

It seem that the subjectivist account is not really able to make sense of perceptual experience as openness to the world, as the mind- independent object of

on 200 genetic marker loci of animals in the reference population and correlation with true autozygosity ¯r for total genome length of 30 Morgans, random mating and different

MaGelLAn 1.0 is primarily used to: (1) optimise the sampling strat‑ egy for molecular analyses; (2) identify and correct pedigree inconsistencies; and (3) identify maternal lineages

Here, we present a simple prediction equation for the SE of the estimated genetic correlation between traits recorded on distinct individuals, for nested full-half sib schemes

We invite human evaluators to examine the tweets identified as family-related from 50 random users, to determine whether each tweet is truly related to family members. As the