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天祝白牦牛OXGR1基因多态性与体尺性状的关联性分析 被引量:1
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作者 王琪 张全伟 +2 位作者 张勇 马友记 赵兴绪 《兽类学报》 CAS CSCD 北大核心 2017年第4期379-388,共10页
为了研究牦牛α-酮戊二酸(盐)受体1(Oxoglutarate receptor 1,OXGR1)基因多态性与其体尺性状的相关性,本文以4-8岁天祝雄性(阉)白牦牛的血液DNA(n=192)为实验材料并构建DNA混合池。通过DNA直接测序法检测OXGR1的核苷酸序列潜在的多态位... 为了研究牦牛α-酮戊二酸(盐)受体1(Oxoglutarate receptor 1,OXGR1)基因多态性与其体尺性状的相关性,本文以4-8岁天祝雄性(阉)白牦牛的血液DNA(n=192)为实验材料并构建DNA混合池。通过DNA直接测序法检测OXGR1的核苷酸序列潜在的多态位点;利用高分辨率熔解曲线分析技术(High Resolution Melting,HRM)进行分型。采用SHESIS软件对OXGR1基因多态位点进行连锁不平衡分析;运用PIC-Calc 0.6软件分析多态信息含量;采用卡方检验检测Hardy-Weinberg平衡;运用SPSS20.0软件对多态位点与体尺性状进行关联分析;运用RNAFOLD、ExPASy和Swiss-model软件对OXGR1基因突变前后的蛋白结构进行预测分析。结果表明:天祝白牦牛OXGR1基因有两个多态位点,分别为347(A/G)和678(G/A),每个位点均有3种基因型(AA、AG和GG),其优势基因型分别为GG和AA。两个SNPs均达到Hardy-Weinberg平衡(P>0.05),存在强连锁不平衡(D’>0.75,R^2>0.33),且均表现为中度多态(0.25<PIC<0.5)。上述位点不同基因型在体斜长、体高、胸围和管围存在显著差异(P<0.05)。分子结构预测显示:347位点处突变为错义突变,其编码的氨基酸由天冬酰胺变为丝氨酸。突变后OXGR1 mRNA二级结构、蛋白质二级结构及三级结构均发生改变。上述结果表明:OXGR1基因可作为牦牛分子育种的候选分子标记,为今后牦牛遗传资源的保护、开发以及新品种的选育提供依据。 展开更多
关键词 牦牛 oxgr1基因 多态性 HRM 体尺性状
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AKG/OXGR1 promotes skeletal muscle blood flow and metabolism by relaxing vascular smooth muscle
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作者 Jinping Yang Guli Xu +15 位作者 Yiming Xu Pei Luo Yexian Yuan Lin Yao Jingjing Zhou Yunlong Zhu Ishwari Gyawali Chang Xu Jinlong Feng Zewei Ma Yuxian Zeng Songbo Wang Ping Gao Canjun Zhu Qingyan Jiang Gang Shu 《Life Metabolism》 2022年第3期285-297,共13页
In response to contraction during exercise,skeletal muscle growth and metabolism are dynamically regulated by nerve action,blood flow,and metabolic feedback.α-Ketoglutarate(AKG),a bioactive intermediate in the tricar... In response to contraction during exercise,skeletal muscle growth and metabolism are dynamically regulated by nerve action,blood flow,and metabolic feedback.α-Ketoglutarate(AKG),a bioactive intermediate in the tricarboxylic acid cycle released during exercise,has been shown to promote skeletal muscle hypertrophy.However,the underlying mechanism of AKG in regulating skeletal muscle development and metabolism is still less known.2-Oxoglutarate receptor 1(OXGR1),the endogenous AKG receptor,is found to be distributed in the vascular smooth muscle(VSM)of skeletal muscles.OXGR1 knockout results in skeletal muscle atrophy,accompanied by decreased expression of myosin heavy chain I(MyHC I),capillary density,and endurance exercise capacity.Furthermore,the study found that dietary AKG supplementation increased mice endurance exercise distance,MyHC I/MyHC IIb ratio,arteriole,and capillary densities in skeletal muscle.Meanwhile,acute AKG administration gradually increased the blood flow in the lower limbs.Further,by using OXGR1 global knockout and OXGR1 VSM-specific(MYH11-Cre×OXGR1-FloxP)knockdown models,we found that OXGR1 in VSM is essential for AKG-induced improvement of skeletal muscle performances.According to the in vitro study,AKG expanded the cell area in VSM with a decreased intracellular pH by OXGR1.Our results demonstrated a novel role of AKG/OXGR1 in VSM of skeletal muscle to regulate blood flow and then enhance slow muscle fiber conversion and capillarization.These findings provide a theoretical basis for the AKG/OXGR1 signaling pathway to maintain human muscle function and improve meat production and livestock and poultry meat quality. 展开更多
关键词 oxgr1 AKG smooth muscle cell skeletal muscle blood flow METABOLISM
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Smooth muscle AKG/OXGR1 signaling regulates epididymal fluid acid–base balance and sperm maturation
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作者 Chang Xu Yexian Yuan +12 位作者 Cha Zhang Yuchuan Zhou Jinping Yang Huadong Yi Ishwari Gyawali Jingyi Lu Sile Guo Yunru Ji Chengquan Tan Songbo Wang Yongliang Zhang Qingyan Jiang Gang Shu 《Life Metabolism》 2022年第1期67-80,共14页
Infertility is a global concern attributed to genetic defects,lifestyle,nutrition,and any other factors that affect the local metabolism and niche microenvironment of the reproductive system.2-Oxoglutarate receptor 1(... Infertility is a global concern attributed to genetic defects,lifestyle,nutrition,and any other factors that affect the local metabolism and niche microenvironment of the reproductive system.2-Oxoglutarate receptor 1(OXGR1)is abundantly expressed in the testis;however,its cellular distribution and biological function of OXGR1 in the male reproductive system remain unclear.In the current study,we demonstrated that OXGR1 is primarily expressed in epididymal smooth muscle cells(SMCs).Aging and heat stress significantly reduced OXGR1 expression in the epididymis.Using OXGR1 global knockout and epididymal-specific OXGR1 knockdown models,we revealed that OXGR1 is essential for epididymal sperm maturation and fluid acid–base balance.Supplementation ofα-ketoglutaric acid(AKG),the endogenous ligand of OXGR1,effectively reversed epididymal sperm maturation disorders caused by aging and heat stress.Furthermore,in vitro studies showed that AKG markedly stimulated the release of instantaneous intracellular calcium from epididymal SMCs and substantially reduced the pH_(i) value in the epididymal SMCs via OXGR1.Mechanistically,we discovered that AKG/OXGR1 considerably increased the expression of Na^(+)/HCO_(3)^(−)cotransporter(NBCe1)mRNA in the epididymal SMCs,mediated by intracellular calcium signaling.The local AKG/OXGR1 system changed the epididymal fluid pH value and HCO_(3)^(−)concentration,thereby regulating sperm maturation via intracellular calcium signaling and NBCe1 mRNA expression.This study for the first time reveals the crucial role of OXGR1 in male fertility and sheds light on the applicability of metabolic intermediates in the nutritional intervention of reproduction. 展开更多
关键词 AKG oxgr1 EPIDIDYMIS acid-base balance sperm maturation
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α-酮戊二酸/酮戊二酸受体1系统对雄性动物睾酮分泌和精子生成的影响 被引量:1
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作者 徐畅 张姹 +4 位作者 谭成全 习欠云 王声会 江青艳 束刚 《动物营养学报》 CAS CSCD 北大核心 2022年第5期3286-3296,共11页
本试验旨在研究α-酮戊二酸(AKG)/酮戊二酸受体1(OXGR1)系统对雄性动物睾酮分泌和精子生成的影响。首先采用免疫荧光检测OXGR1在睾丸组织中的定位。然后以酮戊二酸受体1敲除(OXGR1 knockout,OXGR1KO)小鼠为模型,采用酶联免疫吸附剂测定(... 本试验旨在研究α-酮戊二酸(AKG)/酮戊二酸受体1(OXGR1)系统对雄性动物睾酮分泌和精子生成的影响。首先采用免疫荧光检测OXGR1在睾丸组织中的定位。然后以酮戊二酸受体1敲除(OXGR1 knockout,OXGR1KO)小鼠为模型,采用酶联免疫吸附剂测定(ELISA)法检测血清睾酮含量,运用苏木精-伊红(HE)染色分析睾丸曲细精管空腔面积、睾丸组织形态差异,采用实时荧光定量PCR检测睾丸生精标志基因mRNA表达水平。在急性试验中,选取16只10周龄雄性小鼠,按体重随机分成4组,分别注射0、1、5、10 mg/kg AKG 6 h后检测血清睾酮含量和小鼠攻击性,再选取10周龄雄性小鼠和OXGR1KO小鼠各12只,并按体重随机分成4组,每组注射5 mg/kg AKG 6 h后检测血清睾酮含量。在离体试验中,用不同浓度AKG处理睾丸间质细胞(TM3细胞)24 h后,检测TM3细胞上清液睾酮含量;并使用200μmol/L AKG处理TM3细胞检测细胞内瞬时钙离子浓度。在长期试验中,选取8周龄雄性小鼠和OXGR1KO小鼠各12只,并按体重随机分成4组,分别为WT组、WT+2%AKG组、OXGR1KO组和OXGR1KO+2%AKG组,试验28 d后检测小鼠血清睾酮含量和睾丸曲细精管空腔面积。结果表明:1)OXGR1特异性分布在睾丸间质细胞。2)OXGR1KO可显著或极显著降低小鼠血清睾酮含量和β-微管蛋白Ⅲ(Tubb3)、性别决定基因盒9(Sox9)mRNA相对表达水平(P<0.05或P<0.01)。3)腹腔急性注射5 mg/kg AKG 6 h后,可显著提高小鼠血清睾酮含量(P<0.05),增加小鼠攻击性。4)离体研究表明,AKG以剂量依赖方式极显著上调睾丸间质细胞(TM3)上清液睾酮含量(P<0.01),且200μmol/L AKG可极显著促进TM3细胞瞬时钙离子释放(P<0.01)。5)长期饮水添加2%AKG 4周可极显著提高小鼠血清睾酮含量(P<0.01),极显著减少睾丸曲细精管空腔面积(P<0.01),而OXGR1KO可显著逆转AKG对血清睾酮含量和曲细精管形态变化的影响(P<0.05)。综上所述,AKG作为重要的生物活性代谢中间产物,可通过OXGR1提高雄性动物血清睾酮含量,影响曲细精管发育和精子生成。 展开更多
关键词 Α-酮戊二酸 酮戊二酸受体1 睾酮 空腔面积
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