Alleles and genotypes frequency at the locus c.529 + 27G>C (c.619 + 27G>C)

Alleles and genotypes frequency at the locus c.529 + 27G>C (c.619 + 27G>C)

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The present study was undertaken to analyse the genetic variation in coding sequences, splicing sites and regulatory sequences of FABP4, PPARγ and SCD genes in five breeds of sheep raised in Poland with different purposes: meat (Suffolk, Ile de France), dairy/prolific (Olkuska sheep, Koludzka) and primitive breeds (Polish Mountain Sheep). To identi...

Context in source publication

Context 1
... populations of Ile de France, Suffolk and Polish Mountain Sheep ewes were in genetic Hardy-Weinberg equilibrium in the studied locus. Table 7. and Figure 4. place In the case of the SCD gene, the presence of the transition c.*945G>A (g.20442503C>T) ...

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Citations

... Peroxisome proliferator-activated receptor γ (PPARγ)-a member of the nuclear receptor superfamily-is a ligand-activated transcription factor that regulates biological processes in a variety of tissues, including the placenta [7]. PPARγ plays a key regulatory role in lipid metabolism and promotes adipocyte differentiation [8]. ...
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Trophoblast cells synthesize and secrete prostaglandins (PGs), which are essential for ruminants in early gestation to recognize pregnancy. Hormones in the intrauterine environment play an important role in regulating PGs synthesis during implantation, but the underlying mechanism remains unclear. In this study, co-treatment of sheep trophoblast cells (STCs) with progesterone (P4), estradiol (E2), and interferon-tau (IFN-τ) increased the ratio of prostaglandin E2 (PGE2) to prostaglandin F2α (PGF2α) and upregulated peroxisome proliferator-activated receptor γ (PPARγ) expression, while inhibiting the mechanistic target of rapamycin (mTOR) pathway and activating cellular autophagy. Under hormone treatment, inhibition of PPARγ activity decreased the ratio of PGE2/PGF2α and cellular activity, while activating expression of the mTOR downstream marker—the phosphorylation of p70S6K (p-p70S6K). We also found that the PPARγ/mTOR pathway played an important role in regulating trophoblast cell function. Inhibition of the mTOR pathway by rapamycin increased the ratio of PGE2/PGF2α and decreased the expression of apoptosis-related proteins after inhibiting PPARγ activity. In conclusion, our findings provide new insights into the molecular mechanism of prostaglandin regulation of trophoblast cells in sheep during early pregnancy, indicating that the PPARγ/mTOR pathway plays an important role in PGs secretion and cell viability.