Yang Lei, Tong Mei-Ling, Chi Xia, Zhang Min, Zhang Chun-Mei, Guo Xi-Rong
State Key Laboratory of Reproductive Medicine, Department of Pediatrics, Nanjing Maternity and Child Health Care Hospital Affiliated to Nanjing Medical University, No 123 Tianfei Xiang, Mochou Road, Nanjing 210029, China.
Int J Mol Sci. 2012 Nov 22;13(12):15575-87. doi: 10.3390/ijms131215575.
NYGGF4, an obesity-related gene, is proposed to be involved in the development of insulin resistance; however, the underlying molecular mechanisms remain unclear. In the present analysis, NimbleGen tiling arrays were used to determine the patterns of genomic DNA methylation at CpG islands and promoters in NYGGF4-overexpression adipocytes. A total of 2352 CpG dinucleotides in 2018 genes and 3490 CpG dinucleotides in 3064 genes were found to be hypermethylated or hypomethylated, respectively, in NYGGF4-overexpression adipocytes. Furthermore, gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes(KEGG) pathway analysis revealed enrichment of biological processes associated with energy metabolism and signal transduction events, including the peroxisome proliferator-activated receptor gamma (PPARγ) signaling pathway, and mitogen-activated protein kinases(MAPK) and Ras homolog gene family, member A (RhoA) signaling. These data demonstrate that differentially methylated genes are significantly overrepresented in NYGGF4-overexpression adipocytes, providing valuable clues for further exploration of the role of NYGGF4 in insulin sensitivity regulation.
NYGGF4是一种与肥胖相关的基因,据推测其参与胰岛素抵抗的发生发展;然而,其潜在的分子机制仍不清楚。在本分析中,使用NimbleGen平铺阵列来确定NYGGF4过表达脂肪细胞中CpG岛和启动子处的基因组DNA甲基化模式。在NYGGF4过表达脂肪细胞中,分别发现2018个基因中的2352个CpG二核苷酸和3064个基因中的3490个CpG二核苷酸发生了高甲基化或低甲基化。此外,基因本体(GO)和京都基因与基因组百科全书(KEGG)通路分析显示,与能量代谢和信号转导事件相关的生物学过程富集,包括过氧化物酶体增殖物激活受体γ(PPARγ)信号通路、丝裂原活化蛋白激酶(MAPK)和Ras同源基因家族成员A(RhoA)信号通路。这些数据表明,差异甲基化基因在NYGGF4过表达脂肪细胞中显著富集,为进一步探索NYGGF4在胰岛素敏感性调节中的作用提供了有价值的线索。