首页> 外文期刊>Canadian Journal of Animal Science >Sequence characterization, tissue-specific expression and polymorphism of the porcine intestinal-type fatty acid binding protein gene.
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Sequence characterization, tissue-specific expression and polymorphism of the porcine intestinal-type fatty acid binding protein gene.

机译:猪肠型脂肪酸结合蛋白基因的序列表征,组织特异性表达和多态性。

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The intestinal fatty-acid-binding protein (I-FABP) shows binding specificity for long-chain fatty acids and is proposed to be involved in the uptake of dietary fatty acids and their intracellular transport. In this study, the full-length cDNA of porcine I-FABP gene was obtained by the rapid amplification of cDNA ends (RACE). The nucleotide sequence and the predicted protein sequence share high sequence identity with its mammalian counterparts. Northern hybridization and semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) revealed that porcine I-FABP is expressed in all 12 tissues studied (heart, brain, kidney, skeletal muscle, testis, liver, skin, small intestine, fat, stomach, lymph and pituitary), but a transcript of approximate 620 bp is more abundant in small intestine than in other tissues. The full-length genomic DNA of the porcine I-FABP gene was amplified by PCR. The coding region of the pig I-FABP gene is organized in four exons and spans an approximate 3.5-kb genomic region. Comparative sequencing of four pig breeds revealed a single nucleotide polymorphism (SNP) within exon 1 of which an A-&G substitution at codon 21 changes a codon for lysine into a codon for arginine. The distribution of allele and genotype frequencies differed significantly between indigenous Chinese Zang, Dahe and Yanan breeds (higher frequencies of A and AA) and Western Large White breed (higher frequencies of G and GG, P&0.01). The association analysis using five pig populations suggested that A21G polymorphism was associated with intramuscular fat content, indicating that the I-FABP gene A21G SNP can be a potential molecular marker for intramuscular fat content..
机译:肠道脂肪酸结合蛋白(I-FABP)对长链脂肪酸表现出结合特异性,并被认为与膳食脂肪酸的摄取及其细胞内运输有关。本研究通过快速扩增cDNA末端(RACE)获得了猪I-FABP基因的全长cDNA。核苷酸序列和预测的蛋白质序列与其哺乳动物对应物具有高度的序列同一性。 Northern杂交和半定量逆转录聚合酶链反应(RT-PCR)显示,猪I-FABP在所有研究的12个组织(心脏,脑,肾脏,骨骼肌,睾丸,肝脏,皮肤,小肠,脂肪)中都有表达(胃,淋巴和垂体),但是小肠中大约620 bp的转录物比其他组织中的丰富。通过PCR扩增猪I-FABP基因的全长基因组DNA。猪I-FABP基因的编码区被组织为四个外显子,并跨越一个大约3.5 kb的基因组区域。四个猪品种的比较测序揭示了外显子1内的单核苷酸多态性(SNP),其中第21位密码子的A→G取代将赖氨酸的密码子变为精氨酸的密码子。等位基因和基因型频率的分布在中国本土的藏族,大河和延安品种(AA和AA的频率较高)和西部大白种(G和GG的频率较高,P <0.01)之间存在显着差异。使用五个猪群的关联分析表明,A21G多态性与肌内脂肪含量有关,这表明I-FABP基因A21G SNP可能是肌内脂肪含量的潜在分子标记。

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