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犬过氧化物酶体增殖物激活受体的克隆、表达及多态性研究

Cloning, expression and investigation for polymorphisms of canine peroxisome proliferator-activated receptors.

作者信息

Nishii Naohito, Takasu Masaki, Soe Ok Kar, Maeda Sadatoshi, Ohba Yasunori, Inoue-Murayama Miho, Kitagawa Hitoshi

机构信息

Department of Clinical Veterinary Medicine, United Graduate School of Veterinary Sciences, Gifu University, Japan.

出版信息

Comp Biochem Physiol B Biochem Mol Biol. 2007 Aug;147(4):690-7. doi: 10.1016/j.cbpb.2007.04.011. Epub 2007 Apr 22.

Abstract

Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors implicated in lipid metabolism. In this study, the full-length cDNA of canine PPARbeta and gamma were sequenced, and expression of PPARs was evaluated in normal tissues and primary cultures of adipocytes in dogs, followed by investigations for polymorphisms of canine PPARgamma. Comparison of the deduced amino acid sequences of canine PPARbeta and gamma cDNA with that of human PPARbeta and gamma cDNA revealed 95.9% and 98.2% identity, respectively. PPARbeta expression was ubiquitous and high PPARgamma expression was detected in the subcutaneous and omental adipose tissues, spleen and large intestine. Canine PPARgamma mRNA expression in cultured adipocytes began to increase from 4 days after induction of differentiation, and increased nearly ninefold within 10 days after induction of differentiation. Although expression level of PPARalpha was low in the cultured adipocytes, it slightly increased within 10 days. In contrast, expression of PPARbeta showed only small variations during adipocyte differentiation, though expression levels were relatively high. These results suggest that PPARgamma may play an important role in adipocyte differentiation in dogs. Investigations for polymorphisms of PPARgamma revealed a silent polymorphism, C1362T, in 3 of 92 dogs.

摘要

过氧化物酶体增殖物激活受体(PPARs)是参与脂质代谢的配体激活转录因子。在本研究中,对犬PPARβ和γ的全长cDNA进行了测序,并评估了PPARs在犬正常组织和原代脂肪细胞培养物中的表达,随后对犬PPARγ的多态性进行了研究。犬PPARβ和γ cDNA推导的氨基酸序列与人PPARβ和γ cDNA的比较分别显示出95.9%和98.2%的同一性。PPARβ表达普遍存在,在皮下和网膜脂肪组织、脾脏和大肠中检测到高PPARγ表达。培养的脂肪细胞中犬PPARγ mRNA表达在诱导分化后4天开始增加,并在诱导分化后10天内增加近9倍。虽然培养的脂肪细胞中PPARα表达水平较低,但在10天内略有增加。相比之下,PPARβ的表达在脂肪细胞分化过程中仅显示出微小变化,尽管表达水平相对较高。这些结果表明PPARγ可能在犬脂肪细胞分化中起重要作用。对PPARγ多态性的研究在92只犬中的3只中发现了一个沉默多态性C1362T。

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