The effect of gene SKI polymorphism on carcass traits in pigs

Transkrypt

The effect of gene SKI polymorphism on carcass traits in pigs
Animal Science Papers and Reports vol. 24 (2006) no. 2, 163-168
Institute of Genetics and Animal Breeding, Jastrzębiec, Poland
SHORT REPORT
The effect of gene SKI polymorphism
on carcass traits in pigs
Paweł Urbański1, Mariusz Pierzchała1, Agnieszka Korwin-Kossakowska1,
Jolanta Kurył1, Marian Kamyczek2, Marian Różycki3
1
Polish Academy of Sciences Institute of Genetics and Animal Breeding,
Jastrzębiec, 05-552 Wólka Kosowska, Poland
2
Pig Hybridization Centre, National Research Institute of Animal Production,
Pawłowice, 64-122 Pawłowice, Poland
3
National Research Institute of Animal Production, 32-083 Balice/Cracow, Poland
(Received April 24, 2006, accepted June 06, 2006)
Phosprotein, the product of proto-oncogene SKI, plays a role in the control of cell growth and in
skeletal muscle differentiation. The aim of this study was to characterize the polymorphism of gene
SKI identified with restriction endonuclease BsmAI in gilts of Polish Large White (PLW, n=117)
and Polish Landrace (PL, n=51), and to analyse the relation between the SKI genotypes and carcass
traits. The animals were free of RYR1T allele. In both breeds, the frequency of homozygote CC at
the SKI locus occurred very low. The only significant relations between genotype and carcass traits
were observed in PLW gilts for weight of loin and weight of sirloin.
KEY WORDS: carcass quality / gene polymorphism /pig / SKI
Selection for increased growth rate or decreased backfat thickness was important
in pig breeding during last two decades, based, among others, on OTL identification.
Within this area, one of the methods used is evaluation of candidate genes polymorphism
effect on phenotypic variation [Kurył 2000 – a review].
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P. Urbański et al.
Recently, the SKI proto-oncogene was suggested as potentially influencing
carcass traits in pigs [Stratil et al. 2002]. SKI encodes a nuclear protein, binds to
DNA in association with other cellular factors, and modulates transcription [Berk
et al. 1997]. These proteins are involved in cell proliferation, differentiation and
apoptosis. The gene SKI has also been found implicated in the control of myogenesis
processes [Berk et al. 1997]. Earlier Colmenares and Stavnezer [1989] reported that
the proto-oncogene SKI induces muscle cell differentiation. Transgenic pigs and mice
carrying SKI sequences show marked muscle hypertrophy characterized by myofibretype specificity [Sutrave et al. 1990, Pursel et al. 1992]. The induction of MYOD1
and MYF4 expression by the SKI suggests, that this proto-oncogene acts early in the
pathway, perhaps in the determination step next to MYOD1 and(or) MYF5. Thus,
induction of myofibre hypertrophy suggests the SKI activity during postnatal muscle
growth, perhaps in cooperation with other genes [Colmenares et al. 1991]. In order to
determine a normal function of this gene in vivo, Berk et al. [1997] have disrupted the
mouse SKI gene. The results confirmed its function in skeletal muscle development
and showed a novel role of the factor in the morphogenesis of craniofacial structures
and the central nervous system. But the exact role of the gene in development of
skeletal muscle still remains unclear.
In the porcine SKI mapped to pig chromosome 6, double nucleotide substitution
CG→TC at positions 304-305 resulting in an amino acid substitution in the protein
(Arg→Ser), was described by Stratil et al. [2002]. This polymorphism is located
in exon 1, encoding functional domain responsible for transformation and muscle
differentiation.
The aim of this study was to evaluate the effect of the mutation described on
porcine growth rate and carcass traits. A similar analysis has not been reported in
literature to date.
Material and methods
Included were Polish Large White (PLW, n=117) and Polish Landrace (PL, n=51)
gilts free of RYR1T allele. The pigs were fattened and slaughtered at the Pig Testing
Station of the National Research Institute of Animal Production, Pawłowice near
Leszno Wlkp, Poland. From 25 to 100 kg live body weight the commercial mixed
feed was applied ad libitum. Right carcass side was dissected into lean, fat and bone
according to the procedure described by Różycki [1996]. In the present study the
following traits were considered: weight of right carcass side, weight of ham with
shank, height of loin eye, loin eye area, loin weight, sirloin weight, meat content
of valuable carcass cuts and meat content of carcass. Genomic DNA was isolated
from leukocytes according to Kawasaki [1990]. The SKI genotyping was performed
using PCR/RFLP technique with BsmAI (Alw26I) endonuclease, recognizing G→
C substitution, according to Stratil et al. [2002]. An amplified 350 bp fragment
encompassed part of SKI exon 1. Association analyses were carried out for each of two
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SKI gene polymorphism and carcass traits in pigs
breeds separately using the least squares method of the GLM procedure [Statistical
Analysis Systems Institute Inc. 2001, according to the following model:
where:
Yijkl = µ + Gi + Oj + β(xij - x) + eij
yij – trait measured on ij-th animal;
µ – overall mean;
Gi – effect of SKI genotype;
Oj – sire effect;
β(xij - x) – linear regression for weight of right carcass side (for carcass traits)
and age at slaughter (for growth rate traits);
eij – random error.
Results and discussion
The frequency of genotypes and alleles at the SKI locus is shown in Table 1. The
G305C polymorphism present in exon 1 was identified with enzyme BsmAI. Three
SKI /G305C genotypes were observed in breeds tested, but the frequency of genotype
CC was low in both (11.1% in PLW and 1.96% in PL). In PLW the frequency of
homozygotes GG was similar to that of heterozygotes whereas in PL the most frequent
was GG genotype. Stratil et al. [2002] reported the highest frequency of SKI C allele
in Pietrain pigs, whereas Meishan pigs appeared to be monomorphic for the allele G.
However, one should mention that in a cited study by Stratil et al. [2002] number of
animals of individual breeds was very low (6 and 12, respectively).
Table 1. Frequency of genotypes and alleles at locus SKI in Polish Large White (PLW) and Polish
Landrace (PL) gilts
Breed
Number
of animals
Number and frequency
genotypes
alleles
GG
GC
CC
G
C
PLW
117
50
(42.7%)
54
(46.1%)
13
(11.11%)
0.66
0.34
PL
51
37
(72.5%)
13
(25.4%)
1
(1.96%)
0.85
0.15
A significant relationship between production traits and the genotype at the
SKI locus was observed for two traits and in PLW gilts only (Tab. 2). The tested
transversion – G305C – was found significant for weight of loin and weight of sirloin.
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P. Urbański et al.
Table 2. Least squares means (LSM) and their standard errors (SE) for two carcass traits as
affected significantly by genotype at the SKI locus in Polish Large White pigs
SKI genotype at nucleotide G305C
Carcass trait
Weight of sirloin (kg)
Weight of loin (kg)
GG
GC
CC
LSM
SE
LSM
SE
LSM
SE
0.359Aa
6.769a
0.006
0.089
0.340B
6.556b
0.005
0.084
0.339b
6.749
0.009
0.138
aA...
Within rows means bearing different superscripts differ significantly at: small letters −
P≤0.05; capital − P≤0.01.
The homozygotes of the G allele showed the highest value of these traits, compared to
heterozygotes and homozygotes of allele C. Heterozygotes showed the lowest weight
of loin compared to both homozygotes. Such phenomenon observed earlier for certain
human genes was named a negative (or positive) heterosis – Comings and MacMurray
[2000] – who suggested that if the regulation of the gene is dose-dependent, the
presence of a regulatory sequence in a heterozygous state could modify the gene
function. Similar associations were also observed in our earlier studies regarding
MyoD genes family [Cieślak et al. 2002, Urbański et al. 2005, 2006, WyszyńskaKoko et al. 2006].
We did not observe any significant relation between SKI genotypes and carcass
traits in PL pigs tested in this study. A low number of animals (51 only) may be the
reason for insignificance of associations studied (Tab. 1).
The SKI proto-oncogene has been mapped to chromosome 6 by Stratil et al.
[2002], where two other genes – RYR1 [Fujii et al. 1991] and H-FABP [Gerbens et
al. 1997] – as well as QTLs important for growth rate and carcass traits [Paszek et al.
1999 and Geldermann et al. 2003] have been localized. The RYR1 genotype is known
to affect carcass quality. In the present study, however, this was excluded as the gilts
analysed were free of RYR1T allele. Thus, the observed effect of SKI genotype on
carcass traits has not been modified by RYR1 gene linked to SKI locus.
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Paweł Urbański, Mariusz Pierzchała, Agnieszka Korwin-Kossakowska,
Jolanta Kurył, Marian Kamyczek, Marian Różycki
Analiza wpływu polimorfizmu genu SKI na cechy tuszy świń
Streszczenie
Protoonkogen SKI pełni ważną rolę w procesie wzrostu i rozwoju organizmu oraz jest zaangażowany
w proces rozwoju mięśni szkieletowych. Produktami tego genu są białka jądrowe, uczestniczące, między
innymi, w indukcji procesów miogenezy. Celem badań była charakterystyka polimorfizmu genu SKI świń
dwóch ras hodowanych w Polsce – wielkiej białej polskiej (PLW) i polskiej białej zwisłouchej (PL) – i
ocena wpływu tego polimorfizmu na cechy tuszy. Badaniami objęto zwierzęta wolne od genu RYR1T, aby
wykluczyć wpływ genotypu RYR1 na cechy tuszy. W obu rasach zaobserwowano bardzo niską frekwencję
osobników homozygotycznych CC. Istotne zależności między genotypem a badanymi cechami stwierdzono
tylko w rasie wbp (PLW) i to wyłącznie w odniesieniu do masy polędwicy i masy polędwiczki. Autorzy
wnioskują, że znajomość genotypu SKI może być przydatna w selekcji ukierunkowanej na poprawę
wymienionych cech tuszy, jednak badania te powinny być kontynuowane na materiale obejmującym inne
rasy i linie, aby stwierdzić, czy zaobserwowane zależności mają charakter uniwersalny.
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