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Animal models constructed with hybrid relatedness matrix vs incomplete pedigree: an experimental and simulation approach.

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HAL Id: hal-02809584

https://hal.inrae.fr/hal-02809584

Submitted on 6 Jun 2020

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Animal models constructed with hybrid relatedness matrix vs incomplete pedigree: an experimental and

simulation approach.

Julie Gauzere, Etienne Klein, Sylvie Oddou-Muratorio, Laurène Gay

To cite this version:

Julie Gauzere, Etienne Klein, Sylvie Oddou-Muratorio, Laurène Gay. Animal models constructed with hybrid relatedness matrix vs incomplete pedigree: an experimental and simulation approach.. 4. International Conference on Quantitative Genetics: Understanding Variation in Complex Traits, Jun 2012, Edinburgh, United Kingdom. 2012. �hal-02809584�

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Animal models constructed with hybrid relatedness matrix

vs incomplete pedigree in Fagus sylvatica

Julie Gaüzere*, Etienne Klein*, Sylvie Oddou-Muratorio* and Laurène Gay°

* INRA – U.R.F.M. - Mediterranean Forest Ecology – Avignon – France

° INRA – UMR A.G.A.P. – Genetic improvement and adaptation of Mediterranean and tropical plants

To alleviate the effort associated with generating offspring with complete pedigree information, simplified protocols with incomplete pedigrees have been adopted, like open-pollinated shemes. This solution accept untestable assumptions related to the genetic constitution of the families, the numbers of male parents involved and their contributions. Today, molecular markers provide an alternative way to construct animal models via reconstructed pedigrees or relatedness matrix. However, for some species phenotypic informations are still easier to obtain than molecular informations.

This study aims at judging the estimation errors caused by simplifying assumptions in classical breeding experimentations, and at investigating the efforts that should be allocated to obtain respectively phenotypic and information in quantitative genetic studies in wild population.

Accounting for complex kinship structure markedly changed VA and h² estimates : for the different studied traits, the estimates of h² varied between 0.22 and 0.45 when using paternal information, versus h² between 0.39 and 0.63 assuming only maternal half-sibs.

The best quantitative genetics model is an intermediate between the models (i) and (iii), i.e. the model which include the most genetic and phenotypic information. However, genetic data are rarely available on sampled of this size.

We can optimize the use of genetic information in creating a hybrid relatedness matrix which should contain : information from paternity assignments (complete pedigree), relatedness estimated from markers (Fij) and mean relatedness estimations within and between families. This last point should allow to consider that the paternal contributions to the fertilization are skewed and that mother-tree can be pollinated by only a few male-trees.

N1 900m N2 1100m N4 1400m 11°C 44% Hum. rel. 9,5°C 47% Hum. rel. 7°C 55% Hum. rel.

60 maternal progenies (100 individuals per family)

from 3 wild populations on an altitudinal gradient in the South East of France, transferred in a common garden

Context and aims

Material

● Putatively adaptative and performance

traits measured on 6000 seedlings : height increment and budburst phenology

A subset of 625 offspring and all their

mothers and putative fathers genotyped at 13 microsatellite markers

Conclusion

Mating pattern is highly variable among families

Quantitative genetics simplified protocols can lead

to wrong interpretations since genetic effects can be

confuse with maternal effects

Accounting for paternal relatedness among

individuals greatly affect the estimation of VA and h²

The relevance of constructing a « hybrid »

relatedness matrix incorporating several sources of

available information (incomplete pedigree, paternity

assignments, relatedness estimated from markers)

instead of using simplifying assumptions, will be

tested by simulation approach

Discussion

a) Results of mating pattern analysis

Methods and results

Model (i) 5457 ind Model (ii) 625 ind Model (iii) 625 ind Model (i)

5457 ind Model (ii)625 ind Model (iii)625 ind

DeltaH Budburst 0 0,1 0,2 0,3 0,4 0,5 0,6 0,7 0,8 0 0,1 0,2 0,3 0,4 0,5 0,6 0,7 0,8 0,9

The VA and h² of the traits were estimated :

(i) using the 6000 phenotyped seedlings, and assuming that they were all half-sibs (ii) using the sub-sample of 625 individuals, still assuming that they were all half-sibs

(iii) using the same sub-sample and accounting for the paternal relatedness between

individuals inferred by Cervus analysis

b) Quantitative genetics analysis

➔ High heterogeneity of matings systems among mother-trees

➔ High rates of full sibs and selfing in some families =

assumption of maternal half sibs families violated

Hybrid Matrix

F11 1 1/4 1/2 1/2 1/4 1/4 Fij Family1 Family 1 Family 2 Family 2 F12 ― ― ― 1 1 1 1 1/4 1/4 1/4 F11 ― F11 ― F11 ― F11 ― F11 ― F11 ― F11 ― F12 ― F12 ― F12 ― F12 ― F12 ― F12 ― F―12 F

kl : mean relatedness estimation

within (k=l) and among families

Study species : Fagus sylvatica, a monoecious,

wind-pollinated, highly outcrossed European tree species

ACCAF

F

ij : relatedness coefficient

between individual i and j Cervus analysis with n potential father in each population....and we found x

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