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Molecular characterization and expression analysis of NDUFS4 gene in m. longissimus dorsi of Laiwu pig (Sus scrofa)

机译:NDUFS4基因在大肠杆菌中的分子鉴定与表达分析。莱芜猪背最长肌(Sus scrofa)

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To study the molecular basis of intramuscular fat (IMF) deposition, suppression subtractive hybridization was used to investigate the differences in gene expression between m. longissimus dorsi (LD) of high IMF Laiwu pig group and low IMF Laiwu pig group. From two specific subtractive cDNA libraries, the expression-upregulated clone HL-27 was selected by reverse Northern high-density blot, and then identified to be pig mitochondrial NADH dehydrogenase (ubiquinone) Fe-S protein 4 (NDUFS4). Pig NDUFS4full-length cDNA was cloned by RACE, and contains a 528 bp-open reading frame (ORF) encoding 175 amino acid residues. The derived amino acid sequence of NDUFS4 is well conserved compared with NDUFS4 of various species with higher degree of sequence similarity with other mammalian (86.3–92.6 %) than amphibian, aves, and fishes (70.2–81.1 %), and contains one N-linked glycosylation site, one O-linked glycosylation site, seven Ser phosphorylation sites and five Thr phosphorylation sites. A-G mutation wasfound at nt 122 site of ORF between Laiwu pig and Large White, which results in the K-R mutation at 41 site of protein sequence. Real-time PCR analysis indicated that the level of NDUFS4 mRNA expression was higher in high IMF Laiwu pig group than in lowIMF Laiwu pig group, and in Laiwu pig than in Large White. The tissue expression of the pig NDUFS4 gene showed a tissue-specific pattern: highly expressed in LD muscle, spleen and kidney, but hardly expressed in lung, stomach and large intestine. The possible role of NDUFS4 and its relation to IMF deposition are discussed.
机译:为了研究肌内脂肪(IMF)沉积的分子基础,使用抑制消减杂交技术研究了m。之间的基因表达差异。高IMF莱芜猪组和低IMF莱芜猪组的背最长肌(LD)。从两个特定的减法cDNA文库中,通过反向Northern高密度印迹选择表达上调的克隆HL-27,然后鉴定其为猪线粒体NADH脱氢酶(泛醌)Fe-S蛋白4(NDUFS4)。猪NDUFS4全长cDNA通过RACE克隆,包含一个528 bp的开放阅读框(ORF),编码175个氨基酸残基。与各种物种的NDUFS4相比,NDUFS4的氨基酸序列保守性高,与其他哺乳动物(86.3–26.6%)的序列相似性程度高于两栖动物,八角和鱼类(70.2–81.1%),并且包含一个N-连接的糖基化位点,一个O-连接的糖基化位点,七个Ser磷酸化位点和五个Thr磷酸化位点。在莱芜猪和大白猪之间ORF的nt 122位点发现了A-G突变,导致在蛋白质序列的41位出现了K-R突变。实时PCR分析表明,高IMF的莱芜猪组的NDUFS4 mRNA表达水平高于低IMF的莱芜猪组,和莱芜猪均高于大白猪。猪NDUFS4基因的组织表达显示出组织特异性模式:在LD肌肉,脾脏和肾脏中高表达,而在肺,胃和大肠中几乎不表达。讨论了NDUFS4的可能作用及其与IMF沉积的关系。

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