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Contribution to the establishment of the R-banded
karyotype in dogs
M Moreno-Millán, A Rodero, Fj Alonso, C Falcón
To cite this version:
Contribution
to
the establishment
of the R-banded
karyotype
in
dogs
M
Moreno-Millán
A Rodero FJ Alonso
C
Falcón
Facultad de
Ueterinaria,
Universidad deCordoba,
Laboratorio de
Citogenetica, Departamento
deGen6tica,
14005 -C6rdoba, Spain
(Proceedings
of the 9thEuropean Colloquium
onCytogenetics
of DomesticAnimals;
Toulouse-Auzeville,
10-13July
1990)
karyotype
/
R-banding/
dogThe
diploid
number of the domesticdog
(Canis
familiaris
L)
iscomposed
of78
chromosomes,
all of themmorphologically
acrocentric with theexception
ofthe X chromosome which is submetacentric and the metacentric Y chromosome. Howard-Peebles and
Pryor
(1980)
published
the first results ofR-banding
inthis
species. Mayr
et al(1983)
laterproposed
asystem
ofarranging
R-bands. Wedescribe a new contribution to the canine
karyotype
obtained after treatment withbromodeoxyuridine
(BrdU).
The chromosomes of 4
dogs,
3 males and 1female,
were obtained from culturesof
integral
bloodaccording
to the method of deGrouchy
et al(1964)
slightly
mod-ified for domestic animals. R-bands wereproduced using
a modified version of the method describedby
Di Berardino et al(1985):
20!g/ml
of BrdU under a UVlamp
afterstaining
with1%
orange acridine inphosphate
buffer,
pH
6.8.Pho-tographs
were obtained with a Universal Zeiss R-III fluorescencephotomicroscope
on Kodalith film. Fivemetaphases
per animal wereanalyzed.
Figure
1 shows a malemetaphase. Figure
2presents
theidiogram
with theimages
obtained in the R-band of the
species
studied.The
description
of thebanding
of eachchromosome,
in accordance with the nomenclatureproposed
at the Parisconference,
is as follows: 1: 6positive
bandsseparated
3-to-3 with aprominent
negative
band in themiddle;
2: 5bands,
the most intense one is located in a centralposition;
3: 6 bandsregularly
spaced;
4: 5
positive
bands,
two in the first1/3
and 3 in theremaining
2/3 regularly
spaced,
all of similarintensity;
5: 2 very intensepositive
bands each one locatedcentrally
in the
proximal
and distalhalves;
6: 5bands,
the mostprominent
are located in theproximal
2/3;
7: 4positive
bandsregularly
spaced
with the 2 distal bandsbeing
more
intense;
8: 4positive bands,
but the distal half is morestrongly
fluorescent;
9: 4 bands and one
prominent negative
band at the end of theproximal
1/3;
10: 4positive
bandsregularly
spaced;
11: 1negative
band in theproximal
1/3
bands of similar
intensity
andregularly
spaced;
13:proximal
half veryintensely
stained with 2positive
bands while the distal half has 2bands;
14: 3positive
bands and 1negative
band at theend;
15: the distal2/3
is moreintensely
stained thanthe
proximal
1/3
with 1negative
band betweenthem;
16: 4positive
bands with the mostintensely
labeled one locatedproximally,
close to thecentromere;
17: 3regularly
spaced bands;
18: 3bands,
the distal band ispale;
19: 3 bands of similarintensity
andregularly
spaced;
20: 2 verystrong
positive
bands in the distal half and 1positive
band in theproximal half;
21: 2 very intense bands in the distal2/3;
22: 3
positive bands,
1 in theproximal
1/3;
23: 3regularly
spaced bands;
24: 2prominent positive bands,
each one in ahalf;
25: 3positive
regularly spaced
bands;
26: 2
positive
bands of similarintensity;
27: 3 bands with the 2 distal bandsbeing
more intense and the centromere is
pale;
28: 2positive
bands with the most intenseone located
centrally
and the centromere ispale;
29: 2bands,
theproximal
band isstrongly
fluorescent and the centromere ispale;
30: 2bands,
1 medium and 1distal;
31: 2positive
bands,
theproximal
onebeing
more intense than the distal one; 32:2 very intense bands in the distal
half;
33: 3regularly spaced bands;
34: 2 bandsseparated by
acentral, prominent negative band;
35: 1positive
band at theend;
36: 1prominent positive
band at theend;
37: 2 bands in the distal2/3;
fluorescent; Xq:
4bands,
the central band is the mostintense; Yp:
1pale
band atthe
end;
Yq:
1positive
band at the end.In the same way that certain standards have been studied and established for
the
karyotypes
of otherspecies
of domesticanimals,
we think that it is necessary toinvestigate
further the chromosomes of caninespecies
to attain differentobjectives.
On onehand,
thestudy
and characterization of differentkaryotypes
from anevolutionary
viewpoint
by using high-resolution banding techniques
should beenvisaged;
on theother,
the effect of chromosome anomalies on thefertility
ofthe different breeds of domestic
dogs
should beexplored.
REFERENCES
de
Grouchy
J, Roubin M,Passage
E(1964)
Microtechnique
pour 1’6tude des chromosomes humains apartir
d’une culture deleucocytes sanguins.
Ann Genet7,
45-46Di Berardino
D,
LioiMB,
lannuzzi L(1985)
Identification of nucleolusorganizer
chromo-somes in cattle
(Bos
taurusL) by sequential
silverstaining
+ RBAbanding. Caryotogia
38,
95-102Howard-Peebles