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(1)

in

Rouvier R. (ed.), Baselga M. (ed.).

Rabbit production and genetics in the Mediterranean area Zaragoza : CIHEAM

Options Méditerranéennes : Série A. Séminaires Méditerranéens; n. 17 1991

pages 121-126

Article available on lin e / Article dispon ible en lign e à l’adresse :

--- http://om.ciheam.org/article.php?ID PD F=92605168

--- To cite th is article / Pou r citer cet article

--- Bosch A., Poujardieu B., Rouvier R. Zootech n ical an d gen etic poten tial in crossbreedin g experimen ts an d breed comparison s. In : Rouvier R. (ed.), Baselga M. (ed.). Rabbit production and genetics in the Mediterranean area . Zaragoza : CIHEAM, 1991. p. 121-126 (Options Méditerranéennes : Série A. Séminaires Méditerranéens; n. 17)

---

http://www.ciheam.org/

http://om.ciheam.org/

(2)

Zootechnical and.genetic potential in crossbreeding experiments

and breed comparisons

A. BOSCH*

B. POUJARDIEU**

R. ROUVIER**

* ESCOL4

187,08036 BARCELONA, SPAIN

** INSTITUT NATIONAL DE L4 RECHERCHE AGRONOMIQUE, B.P.

27,31326 CASTANEÏ-TOLOSAN CEDEX, FRANCE

- on involving and

to as well as

effects. Two main models of the available

words:

- zootechnique et génétique dans le cadre d’essais de croisement, et comparaison de races”. Les travaux publiés sur la génétique du lapin dans le cadre de croisements et Comparaisons raciales sont révisés. La construction et l’analyse d’expériences de croisement sont discutées, avec une référence particulière aux effets génétiques d’hétérosis direct, maternel, ainsi qu’à ceux de recombinaison. Deux modèles principaux d’analyse de plans de croisement sontproposés compte tenu de la bibliographie.

: Génétique du lapin, croisement, hétérosis, effets de recombinaison, comparaison de races.

Introduction

animal allows the

exploitation of the genetic

and the biological standpoint. is also analysis of genetic

suggest that we have objective scientifically established to

The aim of this is to show of a

to define the and

its implementation as well as to expose its

A crossbreeding experiment.

A step within

a

process

1980;. 1982;

1982; 1984;

1988) most of the published is a step within a of knowledge acquisition. We shall limit to the knowledge

can help in the choice of the definition of utilization.

by (1984, 1988)

the utilization of in

choice. 1961, of field

we know the management conditions

availabilities et 1973). 1970, public financed defined a national plan of

shall come

a female mated with a meat type

male. the task of of the

Options - - n” 17 - 1992: 121-126

(3)

which ones should be to be selected? and,

of we have to estimate

the

used in within it is

to

The tool

of with

with the the

by selection, shall be

in cages

having as

main activity. the

OF

Within a given types

can be used.

was the by Ouhayoun (1977).

the estimation of specific combining ability became as as the estimation of

combining ability.

Within these types of the most often in

as as the

go the objective is a

to the of

is the main goal. Since knowledge of the specific combining ability is

choice of the the

is developed is

the evaluated.

the following examples (Ouhayoun, 1977) evaluated

station is suitable in this case.

be evaluated at an such as

that of

1986). was

impossible.

A 1077, selected at shows an conditions (30" C and 80%

1984). A of

with autochthonous animals allows the of the

to diffuse to the

to the

This device the

of the action:

is

the knowledge of

of allows the definition

of a diffusion policy.

This last example is that of of an

shows the of

studies which, physiological

knowledge that might be involved, help in the choice the of those susceptible to be adapted.

The aim of is the

acquisition of knowledge which, the

economical and social aspects. is

of success. A of the

to the

the is the choice of

objective. As any an of

is a way of testing a hypothesis in a dialogue between knowledge and

How to construct

a

crossbreeding experiment

involves

of designs.

we will to any

case. to the decomposition of the mean value of

1969; 1990).

The comes assigning

given age

is of

to the of size of is often

To size as is

analogical to the existence of I

on 1982). A t least

in the case of

exists (Chai, 1969). The only is to assign size

assumption of no epistasis (Eisen, 1983), is the addition of

...

if the individual is

if the dam is if

is if the individual comes

at l shows the

is the individual gene value. This will be as

the of the of

- 122 -

(4)

effects effect

individual. They value

of the individual due to the effect of the dam genes

defined as

the which

The of the

utilized both to design

the chosen,

the design of

to the simulation of devices and the of

is also an element of decision (Cunningham

and Connolly, 1989; 1989).

How to analyze a crossbreeding experiment

The aim of the analysis is to obtain the estimates of

the with a maximum

an been the

we want to eliminate

the genetic effects. The way they in the

genetic effects is the two types

of analyzing a

Within the we the estimable

genetic effects as fixed. (1982) has discussed

of the objectives

(1987) of model based upon

(1982) decomposition of the value of the mean. Each two line is

effects, namely: a, 6, aa, a6 and 66; which to additivity, dominance and the

between these two: additive by additive, additive by dominance and dominance by

by (1954).

The second type of model is in

function of the basis of

genetic type effects. The analysis is decomposed in two 1984): estimation of

genotypic values and estimation of genetic effects. The estimated by the estimable coefficients of

of coefficients is

1990). The choice of any function is dictated by means of isolating a genetic effect. The of the of the genetic effect is obtained by the

that defines the the

of the to of an

estimated genetic effect is

A one step calculation can be used by SAS (1986)

estimates of the functions giving the

the genotypic values as well as to significance.

Conceptually, both models applied to the same to the same genetic hypotheses.

can the second in its

genetic elements by the levels of the by

1 and 2).

main effects

be 2 by assigning to each individual

the coefficients of

main genetic effects 3).

with only, of

is:

=

F;

-

+

- - a b = F2- F112 - With

ab = - aal2 - 66 - ab = 6

+

66

F, the

is, which in can be due 6 aa, both. 6 is big and positive we then have a case of

be big since it estimates 6 and 66 aa is big and negative, new

of line A and line

two cases, aa being big and negative,

main

additive effects, aa

1987).

The existence of aa

the development of synthetic since aa can be fixed in the new line.

is to

look of

AA =

c

(aa2ij)k

(5)

is loci (ij), and

assuming summation all of loci (k)

in the lines

1987).

to evaluate AA of

in that

Conclusions

be used to analyze and evaluate the magnitude of and

effects, as well as meaning of main effects

and second These tools can help in

the design of leading to the

of the efficiency of the scheme.

The capacity to estimate the

will depend upon the availability of both physical and

analytical should be

tested and evaluated in basis.

References

lines of

of

of of two selected

of of the W.

AS. Vol. 2~158-166.

(1969): Effects of in

J. 60, 64-70.

An extension of the concept of

882.

J. (1989): Efficient 78, 381-386.

65, 17-23.

components of Z.

the W.

G. (1984):

d'une ambiance chaude et 4-8

(1988): Genetics of

of the W.

Génét. Sél. Anim., 5:83-107.

:

n" 8,29-34.

(Oryctolngus cuniculus). 2nd Cong. of the W.

on Genetics applied to 1982.

of

- 124 -

(6)

1. effects, maternal and grand maternal effects, heterosis, recombination effects.

(A X

effects A

effects

ab ab/2 ab/2

is the of A with and ab is the effect of A with

to (1969).

2. (1982) decomposition of line and crossline average values into main genetic effects and second order interactions.

6 a6 66

-1 -1 1 1 1

1 -1 1 -1 1

1/2 O 1/4 O O

O O O O O

(A X

O 1 O O 1

O 1 O O 1

X (A X -U2 O 1/4 O O

effects A

A

3. Application of (1982) decomposition of line and crossline average values into maternal main effects and maternal second order interactions.

(A X

6 a6 66

1 -1 1 -1 1

-1 -1 1 1 1

-1 -1 1 1 1

1 -1 1 -1 1

O 1 O O 1

O 1 O O 1

O 1 O O 1

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