Kim Hyeng-Soo, Ryoo Zae Young, Choi Sang Un, Lee Sanggyu
School of Life Science, BK21 plus KNU Creative BioResearch Group, Kyungpook National University, Daegu 702-701, Republic of Korea.
Korea Research Institute of Chemical Technology, Daejeon 305-600, Republic of Korea.
Gene. 2015 Jul 1;565(1):15-21. doi: 10.1016/j.gene.2015.03.077. Epub 2015 Apr 17.
Because of the recent discovery of brown adipose tissues tissue in adult humans, brown adipose tissues have garnered additional attention. Many studies have attempted to transform the precursor cells within the white adipocyte cultures to Brite (brown-in-white) cells by using genomic modification or pharmacological activation in order to determine the therapeutic effect of obesity. However, genome-scale analysis of the genetic factors governing the development of white and brown adipose tissues remains incomplete. In order to identify the key genes that regulate the development of white and brown adipose tissues in mice, a transcriptome analysis was performed on the adipose tissues. Network analysis of differentially expressed genes indicated that Trim30 and Ucp3 play pivotal roles in energy balance and glucose homeostasis. In addition, it was discovered that identical biological processes and pathways in the white and brown adipose tissues might be regulated by different genes. Trim30 and Ucp3 might be used as genetic markers to precisely represent the stage of obesity during the early and late stages of adipose tissue development, respectively. These results may provide a stepping-stone for future obesity-related studies.
由于近期在成年人体内发现了棕色脂肪组织,棕色脂肪组织受到了更多关注。许多研究试图通过基因组修饰或药物激活,将白色脂肪细胞培养物中的前体细胞转化为米色(白中带褐)细胞,以确定肥胖症的治疗效果。然而,对控制白色和棕色脂肪组织发育的遗传因素进行的全基因组规模分析仍不完整。为了鉴定调节小鼠白色和棕色脂肪组织发育的关键基因,对脂肪组织进行了转录组分析。对差异表达基因的网络分析表明,Trim30和Ucp3在能量平衡和葡萄糖稳态中起关键作用。此外,还发现白色和棕色脂肪组织中相同的生物学过程和信号通路可能受不同基因调控。Trim30和Ucp3可能分别用作遗传标记,精确表征脂肪组织发育早期和晚期的肥胖阶段。这些结果可能为未来肥胖相关研究提供一个跳板。