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The high-resolution G-banded karyotype of Sus scrofa domestica L
O. Galman, G. Echard
To cite this version:
O. Galman, G. Echard. The high-resolution G-banded karyotype of Sus scrofa domestica L. Genetics
Selection Evolution, BioMed Central, 1991, 23 (suppl.1), pp.113s-116s. �hal-02715412�
The high-resolution G-banded karyotype
of Sus scrofa domestica L
O Galman M Yerle, G Echard
Institut National de la Recherche
Agronomique,
Laboratoire de
Génétique Cellulaire,
BP 27, 31326 Castanet-Tolosan, France(Proceedings
of the 9thEuropean Colloquium
onCytogenetics
of DomesticAnimals;
Toulouse-Auzeville,
10-13July 1990)
high resolution banding
/
karyotype/
pig/
GTG-bandingThe need for a
high-resolution
G-bandedkaryotype
of thepig
has been demon- stratedfollowing
thepublication by
the Committee for a StandardizedKaryotype
of Sus
scrofa (CSKSS, 1988)
of its standardkaryotype
which was based on moder-ately
extended G- and R-banded chromosomes.R 0 nne
et al(1987)
hadpresented
a
high-resolution
R-bandedkaryotype
at the 541 band level but nocorresponding
G-bandedkaryotype
has beenpublished
to date. To fill this gap, this paper describesa
high-resolution
GTG-bandedpig karyotype
at the 539 band level.To obtain mitotic
spreads
at lateprophase, early
andmid-metaphase stages, pig lymphocytes
weresynchronized
with methotrexate(10- 7 M)
for 18 h to block cellsat S
phase,
thensubsequently
releasedby
leucovorin(3
x10- 4 M)
andthymidine
(10-
5 M).
Ethidium bromide(2.5
x10- 5 M)
and colcemid(5
x10- 7 M)
wereemployed
2 and 0.5h, respectively,
before harvest.Hypotonic
treatment, GTG-banding, photography and idiogram
construction have been described elsewhere(Yerle
etal, 1987).
The evolution of G-bands of each of the 38
pig
chromosomes wasanalyzed
fromphotographs
of 52well-spread
and banded mitoses atprogressive
mitoticstages
frommetaphase (CSKSS standard)
to lateprophase.
The finalidiograms
of thechromosomes with 4
haploid karyotypes
at the 539 bandlevel,
shown infigure 1,
take into consideration all 160positive,
278negative
and 101 intermediate bands andsubbands, according
to their relativepositions
andstaining
intensities(Yerle
et
al, 1991). Using
standard landmarks and nomenclature ofmajor
bands as refer-ence
points,
the fate of each band was studied. For eachchromosome,
3 or 4 interme-diate
stages
were constructed to indicate which bands hadsubdivided, appeared
orwere retained in the final
elongated stage.
In mostlong
chromosomes(eg, 1, 4, 6, 8, 9, 13,
14 andX)
landmarks established torecognize
the chromosomes are nolonger evident,
forexample
bandq.4.1
on chromosome 13.However,
in other chromosomessome
bands,
eg,q.2.1.1
of chromosome1,
are still distinct in the definitivestage
(fig 1).
Thepersistence
of centromeric dark bands in the telocentric chromosomes(13-18)
from the standard to the finalstage
should also be noted. Thesebands,
which
correspond
to(or overlap)
the terminal R+ bands(Ronne
etal, 1987),
arelikely
to be the centromeric heterochromatic C-bands which were also stainedduring GTG-banding.
The
karyotype proposed
here can be a useful tool for thestudy
ofcomparative
chromosome
organization
and theprecise mapping
of theporcine
genome(Yerle
etal, 1990).
REFERENCES
Committee for the Standardized
Karyotype
of Susscrofa. (1988)
Standardkaryotype
ofthe domestic
pig.
Hereditas 109, 151-157Ronne
M,
PoulsenBS,
ShibasakiY,
FlouS, Elberg
JJ(1990)
Thehigh-resolution
R-banded
karyotype
of the domesticpig
Susscrofa
domestica L.Cytobios
49, 103-109 YerleM,
EchardG,
Gillois M(1987)
Thehigh
resolutionGTG-banding
pattern of rabbit chromosomes.Cytoge!et
Cell Genet 45, 5-9Yerle M, Gellin J, Dalens
M,
Galman 0(1990)
Localization onpig
chromosome 6 of markers:GPI, APOE,
ENO1 carriedby
chromosomes 1 and 19,using
in situhybridization.
Cytogenet
Cell Genet 54, 86-91Yerle
M,
Galman0,
Echard G(1991)
Thehigh
resolution G-T-Gbanding
pattern ofpig
chromosomes.