研究报告

腹部脂肪组织APN基因DNA甲基化及mRNA表达与维吾尔族T2DM的相关性

展开
  • 1. 石河子大学,新疆地方病与民族高发病教育部重点实验室,新疆石河子 832000; 2. 石河子大学医学院第一附属医院心内科,新疆石河子 832000
张君,博士,副教授,研究方向:肥胖及代谢相关疾病病因学研究。E-mail: zhangjunyc@163.com张望强,硕士,主治医师,研究方向:临床心血管病。E-mail: 616692381@qq.com张君和张望强并列第一作者。

收稿日期: 2014-06-19

  修回日期: 2014-10-11

  网络出版日期: 2015-02-10

基金资助

石河子大学重大科技攻关计划项目(编号:gxjs2012-zdgg02)和石河子大学高层次人才科研启动资金专项(编号:RCZX201230)资助

Correlation between type 2 diabetes and DNA methylation and mRNA expression of APN in abdominal adipose tissues in Xinjiang Uygur population

Expand
  • 1. The Key Laboratory of Xinjiang Endemic and Ethnic Disease, Ministry of Education , Medicine School of Shihezi University, Shihezi 832000,China;
    2. Department of Cardiology, First Affiliated Hospital, Medicine School of Shihezi University, Shihezi 832000,China

Received date: 2014-06-19

  Revised date: 2014-10-11

  Online published: 2015-02-10

摘要

为探讨APN基因启动子区DNA甲基化及mRNA表达与新疆维吾尔族T2DM发生、发展的相关性,文章选择新疆维吾尔族正常个体50例、肥胖个体48例、肥胖伴T2DM个体26例,收集腹部网膜脂肪组织,利用变性高效液相色谱技术检测APN基因启动子区DNA甲基化情况,应用Real-time PCR方法检测APN 基因mRNA表达情况。结果显示,APN基因启动子区DNA甲基化阳性率在正常对照(34%)、肥胖(47.9%)及T2DM组(65.4%)逐渐增加,差异具有统计学意义(P<0.05)。Real-time PCR结果显示,正常对照组APN mRNA相对拷贝数(0.7162)显著高于肥胖(0.4244)及T2DM组(0.4093),差异具有统计学意义(P<0.05)。非T2DM个体相关性分析提示,APN mRNA相对拷贝数与空腹血清葡萄糖(Fasting plasma glucose, FPG)、糖化血红蛋白(Glycosylated hemoglobin, HbA1c)、甘油三酯(Triglyceride, TG)水平显著负相关(P<0.05)。APN基因启动子区DNA甲基化与其mRNA表达负相关,甲基化阳性组相对拷贝数(0.2700)显著低于阴性组(0.7870),差异具有统计学意义(P<0.01)。以上结果提示,APN基因启动子区DNA甲基化通过抑制其 mRNA表达导致糖脂代谢紊乱,可能参与了新疆维吾尔族肥胖及T2DM的发生、发展过程。

本文引用格式

张君, 张望强, 丁毓磊, 许彭, 王婷婷, 徐文静, 陆环, 刘宗智, 谢建新 . 腹部脂肪组织APN基因DNA甲基化及mRNA表达与维吾尔族T2DM的相关性[J]. 遗传, 2015 , 37(3) : 269 -275 . DOI: 10.16288/j.yczz.14-199

Abstract

To investigate the relationship between type 2 diabetes mellitus (T2DM) onset and development and mRNA expression and promoter methylation of adiponectin (APN) gene in abdominal adipose tissues of Xinjiang Uygur population, abdominal adipose tissues of omentum were collected and divided into control, obesity and T2DM groups. The status of APN promoter methylation was detected by denaturing high performance liquid chromatography (DHPLC), while the mRNA expression level of APN was detected by RT-PCR. Results show that methylation positive rate of APN was at the lowest level in control, middel in obesity and highest in T2DM groups, and the differences are statistically significant. Comparing the APN mRNA relative copy number of adipose tissue in each group, we found that the relative copy number of APN in control group is significantly higher than that of obesity and T2DM groups. There is a negative correlation between the mRNA expression level of APN in abdominal adipose tissue and fasting plasma glucose (FPG), glycosylated hemoglobin (HbA1c) and triglyceride (TG) level. There is a negative correlation in DNA promoter methylation and mRNA expression of APN gene. Relative copy number of APN in DNA methylation positive group is significantly lower than that of the negative group. In conclusion, increased APN promoter methylation results in decreased mRNA expression, which induces glucose and lipid metabolic disorder, thus contributing to the initiation and development of T2DM in Xinjiang Uygur population.

参考文献

[1] Maier S, Olek A. Diabetes: a candidate disease for efficient DNA methylation profiling. J Nutr , 2002, 132(8): 2440S-2443S.
[2] Barr&#x000e8;s R, Osler ME, Yan J, Rune A, Fritz T, Caidahl K, Krook A, Zierath JR. Non-CpG methylation of the PGC-l&#x003b1; promoter through DNMT3B controls mitochondrial density. Cell Metab , 2009, 10(3): 189-198.
[3] 霍丽梅, 宋光耀, 叶蔚. 脂联素与2型糖尿病发生发展的研究进展. 临床汇萃, 2005, 20(1): 54-56.
[4] 徐忠星, 张和占, 买买提&#x000b7;西日甫, 买买提阿不拉艾山, 库热西江&#x000b7;托乎提, 程钦, 董宇莉, 依米提, 艾山江. 新疆墨玉县维吾尔族糖尿病患病率调查. 中国基层医药, 2002, 9(3): 221.
[5] Scherer PE, Williams S, Fogliano M, Baldini G, Lodish HF. A novel serum protein similar to C1q, produced exclusively in adipocytes. J Biol Chem , 1995, 270(45): 26746-26749.
[6] Yamauchi T, Kamon J, Waki H, Terauchi Y, Kubota N, Hara K, Mori Y, Ide T, Murakami K, Tsuboyama-Kasaoka N, Ezaki O, Akanuma Y, Gavrilova O, Vinson C, Reitman ML, Kagechika H, Shudo K, Yoda M, Nakano Y, Tobe K, Nagai R, Kimura S, Tomita M, Froguel P, Kadowaki T. The fat-derived hormonead-iponectin reverses insulin resistance associated with both lipoatrophy and obesity. Nat Med , 2001, 7(8): 941-946.
[7] Hotta K, Funahashi T, Arita Y, Takahashi M, Matsuda M, Okamoto Y, Iwahashi H, Kuriyama H, Ouchi N, Maeda K, Nishida M, Kihara S, Sakai N, Nakajima T, Hasegawa K, Muraguchi M, Ohmoto Y, Nakamura T, Yamashita S, Hanafusa T, Matsuzawa Y. Plasma concentrations of a novel, adipose-specific protein, adiponectin, in type 2 diabetic patients. Arterioscler Thromb Vasc Bio , 2000, 20(6): 1595-1599.
[8] Abbasi F, Chu JW, Lamendola C, McLaughlin T, Hayden J, Reaven GM, Reaven PD. Discrimination between obesity and insulin resistance in the relationship with adiponectin. Diabetes , 2004, 53(3): 585-590.
[9] C&#x000f4;t&#x000e9; M, Mauri&#x000e8;ge P, Bergeron J, Alm&#x000e9;ras N, Tremblay A, Lemieux I, Despr&#x000e9;s JP. Adiponectinemia in visceral obesity: impact on glucose tolerance and plasma lipo protein and lipid levels in men. J Clin Endocrinol Metab , 2005, 90(3): 1434-1439.
[10] Lindsay RS, Funahashi T, Hanson RL, Matsuzawa Y, Tanaka S, Tataranni PA, Knowler WC, Krakoff J. Adiponectin and development of type 2 diabetes in the pima Indian population. Lancet , 2002, 360(9326): 57-58.
[11] Bobbert T, Rochlitz H, Wegewitz U, Akpulat S, Mai K, Weickert MO, M&#x000f6;hlig M, Pfeiffer AF, Spranger J. Changes of adiponectin oligomer composition by moderate weight reduction. Diabetes , 2005, 54(9): 2712-2719.
[12] Maeda N, Shimomura I, Kishida K, Nishizawa H, Matsuda M, Nagaretani H, Furuyama N, Kondo H, Takahashi M, Arita Y, Komuro R, Ouchi N, Kihara S, Tochino Y, Okutomi K, Horie M, Takeda S, Aoyama T, Funahashi T, Matsuzawa Y. Diet-induced insulin resistance in mice lacking adiponectin/ACRP30. Nat Med , 2002, 8(7): 731-737.
[13] Kubota N, Terauchi Y, Yamauchi T, Kubota T, Moroi M, Matsui J, Eto K, Yamashita T, Kamon J, Satoh H, Yano W, Froguel P, Nagai R, Kimura S, Kadowaki T, Noda T. Disruption of adiponectin causes insulin resistance and neointimal formation. J Biol Chem , 2002, 277(29): 25863- 25866.
[14] Hotta K, Funahashi T, Bodkin NL, Ortmeyer HK, Arita Y, Hansen BC, Matsuzawa Y. Circulating concentrations of the adipocyte protein adiponectin are decreased in parallel with reduced insulin sensitivity during the progression to type 2 diabetes in rhesus monkey. Diabetes , 2001, 50(5): 1126-1133.
[15] Dwivedi RS, Herman JG, McCaffrey TA, Raj DS. Beyond genetics: epigenetic code in chronic kidney disease. Kidney Int , 2011, 79(1): 23-32.
[16] Bechtel W, McGoohan S, Zeisberg EM, M&#x000fc;ller GA, Kalbacher H, Salant DJ, M&#x000fc;ller CA, Kalluri R, Zeisberg M. Methylation determines fibroblast activation and fibrogenesis in the kidney. Nat Med , 2010, 16(5): 544-550.
[17] Laborie LB, Mackay DJG, Temple IK, Molven A, S&#x000f8;vik O, Nj&#x000f8;lstad PR. DNA hypomethylation, transient neonatal diabetes, and prune
文章导航

/