Ruyter B, Andersen O, Dehli A, Ostlund Farrants A K, Gjøen T, Thomassen M S
AKVAFORSK, Institute of Aquaculture Research, As, Norway.
Biochim Biophys Acta. 1997 Oct 18;1348(3):331-8. doi: 10.1016/s0005-2760(97)00080-5.
A cDNA fragment which encodes salmon peroxisome proliferator activated receptor y (sPPARgamma) was amplified by PCR from the liver of Atlantic salmon (Salmo salar L.). The fragment was 627 bp long. The sequence of the amplified PCR product was similar to the PPARgamma of mouse and hamster. 59% of the bases were identical. Northern blot analysis of salmon liver mRNA showed that the amplified sPPARgamma fragment hybridised to three specific transcripts of lengths 1.6, 2.4 and 3.3 kb. Clofibric acid and bezafibrate, administered to salmon hepatocytes in culture, resulted in a 1.7-fold increase of the 1.6 kb sPPARgamma transcript. The activity of acyl-CoA oxidase also increased approx. 1.7-fold after administration of fibrates. These results indicate that PPAR is an important factor in mediating enzymatic response to fibrates in fish.
通过聚合酶链反应(PCR)从大西洋鲑(Salmo salar L.)肝脏中扩增出一个编码鲑鱼过氧化物酶体增殖物激活受体γ(sPPARγ)的cDNA片段。该片段长627 bp。扩增的PCR产物序列与小鼠和仓鼠的PPARγ相似,59%的碱基相同。对鲑鱼肝脏mRNA进行Northern印迹分析表明,扩增的sPPARγ片段与长度分别为1.6、2.4和3.3 kb的三种特异性转录本杂交。在培养的鲑鱼肝细胞中施用氯贝酸和苯扎贝特后,1.6 kb的sPPARγ转录本增加了1.7倍。施用贝特类药物后,酰基辅酶A氧化酶的活性也增加了约1.7倍。这些结果表明,PPAR是介导鱼类对贝特类药物酶促反应的重要因素。