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αS1-CnD, another allele associated with a decreased
synthesis rate at the caprine αS1-casein locus
M.F. Mahé, F. Grosclaude
To cite this version:
Note
α
S1
-Cn
D
,
another allele associated with
a
decreased
synthesis
rate at
the
caprine α
S1
-casein
locus
M.F. Mahé
F.
Grosclaude
Institut National de la Recherche
Agronomique,
Laboratoire deGénétique Biochimique.
Centre deJouy-en-Josas,
78350Jouy-en-Josas,
France(received
20September
1988,accepted
15 November1988)
Summary —
A seventh allele of thecaprine a
s
,--asein
locus, called!X
S1-Cn
D
,
was observed inFrench
Alpine
and Saanen breeds. Itsfrequency
in alarge
herd (AM 98) was 0.025. Like!X
S1-Cn
B
-,
!X
S1-Cn
F
and!X
S1-Cn
o
,
this allele is associated with a decreasedsynthesis
rate, itsapproximate
mean contribution
being
0.6 - 0.8g/I,
very close to that of!X
S1-Cn
F
.
goat -
<X
s1
-caseln - polymorphism - quantitative
variationsRésumé —
<X
s1
-Cn
D
,
un autre allèle à taux desynthèse
réduit au locus de la caséineo
si
-caprine.
Unseptième
allèle du locus de la caséinea
S1
-caprine,
as!!no,
a été observé dans les racesAlpine
et Saanenfrançaises.
Safréquence
dans ungrand troupeau ( N=198)
était de0,025. Comme
a
S1
-Cn
B
-,
a
S1
-
C
n
F
eta
,
a
-Cn
S1
cet allèle est associé à un taux desynthèse
réduit, sa contribution moyenne étant d’environ 0,6 à 0,8g4,
donc trèsproche
de celled as!!nF.
chèvre - caséine as, -
polymorphisme -
variationsquantitatives
Introduction
Grosclaude et al.
(1987)
haverecently
concluded that thepolymorphism
ofgoat
cx
s1
-casein
is under the control of a minimum of 6 alleles. Allelesc
x
S1-Cn
A
,
c
x
S1-Cn
B
andc
x
S1-Cn
c
were found to be associated with ahigh c
x
s1-casein
content(approximate
meancontribution of each allele
being
3.6g/1) compared
toc
x
S1-Cn
F
anda
si
-Cn"
which areassociated
respectively
with a low content(0.6 g/1)
and an intermediate content(1.6
g/I),
whilec
x
S1-Cn
o
appeared
to be a true null allele.In the same
publication,
the authors mentioned the presence in theelectrophoregrams
of some
milks,
of an additionalband,
called x, whichreacted
inimmunoblotting
withanti-a
s1
-casein
antibodies. We show in thepresent
note that this bandcorresponds
inMaterial and Methods
Individual milk
samples
were obtained from the &dquo;Station deTestage Caprin&dquo;
nearMois-sac, Sainte-Croix Vall6e
Frangaise,
France or fromprivate
farms located in west central France. Alltechniques
were as described in Grosclaude etal.(1987).
Results and Discussion
Band x
(Fig.
2 in Grosclaude etal.,
1987),
hereafter calledD,
migrates slightly
moreslowly
than(3-casein (Fig.
1)
inSDS-polyacrylamide gel.
Because of unavoidable varia-tions in theelectrophoretic
conditions,
this band may be maskedby
the(i-casein
band,
but,
in all cases, its presence can be ascertainedby immunoblotting.
In order to establish the
genetic
determinism of fractionD,
ourfamily
data werescreened for the presence of sires
transmitting
this fraction to theirdaughters.
One suchsire,
numberedA316,
wasfound,
with a total of 16dam-daughter pairs.
In the progeny ofthis
sire,
fraction Dappeared
to be controlledby
an allele of the locusa
si
-Cn
because itwas transmitted in atternance with variant
F,
theproportion
of the 2 classes ofdaughters
not
being significantly
different from the 1: 1 ratio(Table
I).
In
addition,
12 damspossessed
fractionD,
together
with either variant F(9 cases)
orvariant B-
(3 cases). Except
in onedam-daughter
pair, suspected
to be a case offrom sires which did not transmit fraction
D,
8 did and 12 did not receiveD,
aproportion
which
again
was notsignificantly
different from the 1: 1 ratio.Grosclaude et al.
(1987) reported
that,
curiously,
fraction x(here D),
present
in themilk of certain
dams,
was not transmitted to theirdaughters,
an observation at variance with the conclusions of thepresent
note. Re-examination of thesurviving dam-daughter
pairs
among the 7 consideredby
these authorssuggests
theprobable
occurrence of 2parentage
errors in thissample.
The non-transmission of fraction D in the 5remaining
pairs
is attributable to mere chance(P=
0.03).
Allele
a
S1
-Cn
D
is the seventh allele identified at thegoat
as!!asein
locus. Itsfrequency
in thelarge Alpine
herd of Moissac(N
=198)
was 0.025. It was also observedin the Saanen breed. Grosclaude et al.
(1987)
estimated that thefrequencies
ofa
s
,-Cn
O
were 0.05 in
Alpine
and 0.03 in Saanen. Because in their dataa
S1
-Cn
D
was notdistin-guished
froma
s
,-Cn
O
,
these values in factapply
to the combinedfrequencies
ofa
S1
-Cn
o
anda
S1
-Cn
D
.
Thefrequencies
of each of these 2 alleles are thus rather low inboth breeds.
On
immunoblots,
as well as onSDS-polyacrylamide gels,
varianta
s
,-CnD
appearsmuch weaker than variants
a
S1
-CnA,
B or C. Quantification of this variantby
rocket-immunoelectrophoresis,
carried out on individual milksamples
from four animals with thegenotype
as!-Cn!iF,
indicated that theapproximate
mean contribution of allelea
s
,-Cn
D
was = 0.6 - 0.8
g/I,
a lowvalue,
close to that found forF
a
-Cn
S1
(0.6
g/I).
Allelea
si
-Cn
D
is thus the fourth out of a total of 7 alleles associated with a decreasedsynthesis
rate atthe
goat
ag
i
-casein
locus. The biochemicalparticularities
of varianta
S1
-CnD
are underAcknowledgments
We thank J. Bouillon, A.
Maingot,
A. Piacere, G. Ricordeau and J.-P.Sigwald
for their constant and valuablehelp
and N. Mazure for her skillful assistance.Reference
Grosclaude F., Mah6 M.-F.,