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| 陆川猪黑皮质激素受体4基因克隆及序列分析 | |
| 引用本文： | 谢婉,刘明君,何剑雄,申玉建,陈宝剑,关志惠,张名媛,郭亚芬,兰干球,蒋钦杨,杨秀荣,梁晶,谢炳坤. 陆川猪黑皮质激素受体4基因克隆及序列分析[J]. 中国畜牧兽医, 2018, 45(2): 320-329. DOI: 10.16431/j.cnki.1671-7236.2018.02.005 |
| 作者姓名： | 谢婉 刘明君 何剑雄 申玉建 陈宝剑 关志惠 张名媛 郭亚芬 兰干球 蒋钦杨 杨秀荣 梁晶 谢炳坤 |
| 作者单位： | 1. 广西大学动物科学技术学院, 南宁 530004; 2. 广西壮族自治区畜牧研究所, 广西家畜遗传改良重点实验室, 南宁 530001; 3. 广西医科大学实验动物中心, 南宁 530021 |
| 基金项目： | 国家自然科学基金（31360544） |
| 摘 要： | 试验旨在对陆川猪黑皮质激素受体4（melanocortin-4 receptor，MC4R）基因进行克隆及相关信息学分析。通过提取陆川猪背最长肌总RNA，采用RT-PCR、克隆等方法获得含目的基因MC4R的质粒pMD18-T-MC4R，经菌落PCR和测序鉴定正确后，应用相关生物信息学软件对陆川猪MC4R基因的理化性质、蛋白质的结构、修饰结构和亚细胞定位等进行预测分析。结果表明，MC4R基因CDS区长999 bp，编码332个氨基酸，与NCBI上公布的野猪MC4R基因序列中的CDS区存在4个碱基差异，其中175和906 bp处为同义突变，110和278 bp处为错义突变，分别引起第37位谷氨酸变为甘氨酸和第93位缬氨酸变为丙氨酸。同源性比对结果发现，MC4R基因在不同物种及进化的过程中具有较高的保守性。陆川猪MC4R蛋白有明显的疏水区域，不存在信号肽，但有7个跨膜结构域，其编码蛋白的二级结构元件有α-螺旋、延伸链、β-转角和无规则卷曲。修饰结构预测表明，MC4R蛋白存在多处N糖基化位点，但无O糖基化位点，可能主要分布于内质网和囊泡。本研究成功克隆了陆川猪MC4R基因，为更好地开发利用地方品种陆川猪及其繁育奠定理论基础。 |
| 关 键 词： | 陆川猪 MC4R基因 克隆 |
| 收稿时间： | 2017-07-27 |
Cloning and Sequence Analysis of MC4R Gene in Luchuan Pig |
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| XIE Wan,LIU Mingjun,HE Jianxiong,SHEN Yujian,CHEN Baojian,GUAN Zhihui,ZHANG Mingyuan,GUO Yafen,LAN Ganqiu,JIANG Qinyang,YANG Xiurong,LIANG Jing,XIE Bingkun. Cloning and Sequence Analysis of MC4R Gene in Luchuan Pig[J]. China Animal Husbandry & Veterinary Medicine, 2018, 45(2): 320-329. DOI: 10.16431/j.cnki.1671-7236.2018.02.005 | |
| Authors: | XIE Wan LIU Mingjun HE Jianxiong SHEN Yujian CHEN Baojian GUAN Zhihui ZHANG Mingyuan GUO Yafen LAN Ganqiu JIANG Qinyang YANG Xiurong LIANG Jing XIE Bingkun |
| Affiliation: | 1. College of Animal Science & Technology, Guangxi University, Nanning 530004, China; 2. Guangxi Key Laboratory of Livestock Genetic Improvement, Guangxi Institute of Animal Sciences, Nanning 530001, China; 3. Laboratory Animal Center, Guangxi Medical University, Nanning 530021, China |
| Abstract: | This study was aimed to clone melanocortin-4 receptor(MC4R) gene of Luchuan pig and analyze its genetic structure with bioinformatic software. The recombination plasmid pMD18-T-MC4R was constructed with RT-PCR and cloning methods, and detected by colony PCR and sequencing. After successfully constructed the recombination plasmid pMD18-T-MC4R, the further analysis of physical and chemical properties, structure of protein and modification and the subcellular localization were proceeded. The results showed that the cloned MC4R gene fragment included a 999 bp whole length CDS and encoded 332 amino acids. Compared with MC4R gene of Sus scrofa submission in NCBI, there were four base mutations of MC4R gene in Luchuan pig, two mutations at 175 and 906 bp were the same sense mutations,the other two mutations at 110 and 278 bp were the mis-sense mutations, causing glutamic acid converted to glycine and valine converted to alanine in 37 and 93 amino acid residues, respectively. Homology analysis indicated that MC4R was evolutionarily conserved in different species. Seven transmembrane helical regions, several N-glycosylation sites and distinct hydrophobic region were found, but no signal peptide and potential phosphorylation exited in MC4R protein, which might distribute mainly in the endoplasmic reticulum and vacuolar. The elements in the second structure of encoded protein were α-helix, extended strand,β-turn and random coil. The Luchuan pig MC4R gene was successfully cloned in this study, and provided a foundation for further studying on developing and utilizing the local species Luchuan pig and its breeding. |
| Keywords: | Luchuan pig MC4R gene clone |
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