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Adiponectin Gene Variation -4522C/T Is Associated with Type 2 Diabetic Obesity and Insulin Resistance in Chinese 被引量:2
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作者 刘合焜 陈素云 +4 位作者 张思仲 肖翠英 任艳 田浩明 李雪飞 《Journal of Genetics and Genomics》 SCIE CAS CSCD 北大核心 2007年第10期877-884,共8页
The authors investigated the possible association of -4522C/T variation of adiponectin gene with coronary heart disease (CHD) and type 2 diabetes mellitus (T2DM). Genotyping of SNP --4522C/T in 304 patients with C... The authors investigated the possible association of -4522C/T variation of adiponectin gene with coronary heart disease (CHD) and type 2 diabetes mellitus (T2DM). Genotyping of SNP --4522C/T in 304 patients with CHD, 389 patients with T2DM, and 405 age and sex-matched healthy control subjects was carried out by means of PCR-RFLP approach. No significant difference in the genotype or allele frequencies was found, either between patients with CHD and control subjects, or between patients with T2DM and control subjects. However, in the subgroup analysis, an association of the TAr genotype and T allele with type 2 diabetes combined with obesity (BMI ≥ 25 kg/m2) was found (P = 0.014 and P = 0.034, respectively). Also the homeostasis model assessment of insulin resistance (HOMA-IR) in T2DM patients with T/T genotype was significantly higher than that in T2DM patients carrying C allele (P = 0.0069). The authors' findings for the first time demonstrated that SNP --4522 in the adiponectin gene was associated with T2DM that combined with obesity and higher insulin resistance index in patients with T2DM. This indicated that the variation might associate with an increased susceptibility to type 2 diabetic obesity and insulin resistance. But -4522C/T polymorphism did not contribute to the susceptibility of CHD. 展开更多
关键词 ADIPONECTIN single nucleotide polymorphism coronary heart disease type 2 diabetes insulin resistance
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小鼠睾丸组织特异表达基因Rnf148的鉴定及其编码E3泛素连接酶的功能分析 被引量:1
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作者 刘运强 陶大昌 +3 位作者 廖顺尧 杨元 马用信 张思仲 《四川大学学报(医学版)》 CAS CSCD 北大核心 2014年第1期1-5,共5页
目的研究小鼠Rnf148基因表达的时空特异性及其环指结构域的E3泛素连接酶功能。方法提取不同成年小鼠组织、不同胚胎期组织和出生后小鼠睾丸组织的总RNA,通过实时荧光RT-PCR和Northern杂交分析小鼠Rnf148基因的表达谱。构建包含整个Rnf14... 目的研究小鼠Rnf148基因表达的时空特异性及其环指结构域的E3泛素连接酶功能。方法提取不同成年小鼠组织、不同胚胎期组织和出生后小鼠睾丸组织的总RNA,通过实时荧光RT-PCR和Northern杂交分析小鼠Rnf148基因的表达谱。构建包含整个Rnf148蛋白的环指结构域与谷胱甘肽-S-转移酶(GST)的融合蛋白原核表达载体,在BL21细菌中诱导表达后,经GST琼脂糖凝胶纯化GST-Rnf148重组蛋白。体外泛素化反应试验检测GST-Rnf148重组蛋白的E3泛素连接酶功能。结果在小鼠13种不同器官组织中,Rnf148mRNA仅存在于睾丸组织中。进一步Northern杂交验证了只在小鼠睾丸组织表达一个1.2kb左右的Rnf148基因mRNA片段。小鼠Rnf148基因在胚胎期及出生后3周内不表达,出生后21d开始表达,25d后达到表达高峰并一直持续表达。实验成功诱导表达并纯化了GST-Rnf148重组蛋白,体外蛋白泛素化反应显示该重组蛋白具有E3泛素连接酶的功能。结论小鼠Rnf148基因特异地表达在出生3周后的睾丸组织中,Rnf148蛋白的环指结构域具有泛素连接酶活性。 展开更多
关键词 小鼠 Rnf148基因 睾丸特异表达 环指结构域 E3泛素连接酶
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