Villarroya Francesc, Peyrou Marion, Giralt Marta
Department of Biochemistry and Molecular Biomedicine, Institut de Biomedicina (IBUB), University of Barcelona, Barcelona, Catalonia, Spain; CIBER Fisiopatología de la Obesidad y Nutrición, Instituto de Salud Carlos III, Spain; Institut de Recerca Pediàtrica Sant Joan de Déu, Barcelona, Catalonia, Spain.
Department of Biochemistry and Molecular Biomedicine, Institut de Biomedicina (IBUB), University of Barcelona, Barcelona, Catalonia, Spain; CIBER Fisiopatología de la Obesidad y Nutrición, Instituto de Salud Carlos III, Spain; Institut de Recerca Pediàtrica Sant Joan de Déu, Barcelona, Catalonia, Spain.
Biochimie. 2017 Mar;134:86-92. doi: 10.1016/j.biochi.2016.09.017. Epub 2016 Oct 5.
Regulated transcription of the uncoupling protein-1 (UCP1) gene, and subsequent UCP1 protein synthesis, is a hallmark of the acquisition of the differentiated, thermogenically competent status of brown and beige/brite adipocytes, as well as of the responsiveness of brown and beige/brite adipocytes to adaptive regulation of thermogenic activity. The 5' non-coding region of the UCP1 gene contains regulatory elements that confer tissue specificity, differentiation dependence, and neuro-hormonal regulation to UCP1 gene transcription. Two main regions-a distal enhancer and a proximal promoter region-mediate transcriptional regulation through interactions with a plethora of transcription factors, including nuclear hormone receptors and cAMP-responsive transcription factors. Co-regulators, such as PGC-1α, play a pivotal role in the concerted regulation of UCP1 gene transcription. Multiple interactions of transcription factors and co-regulators at the promoter region of the UCP1 gene result in local chromatin remodeling, leading to activation and increased accessibility of RNA polymerase II and subsequent gene transcription. Moreover, a commonly occurring A-to-G polymorphism in close proximity to the UCP1 gene enhancer influences the extent of UCP1 gene transcription. Notably, it has been reported that specific aspects of obesity and associated metabolic diseases are associated with human population variability at this site. On another front, the unique properties of the UCP1 promoter region have been exploited to develop brown adipose tissue-specific gene delivery tools for experimental purposes.
解偶联蛋白-1(UCP1)基因的转录调控以及随后的UCP1蛋白合成,是棕色和米色/明亮脂肪细胞获得分化的、具有产热能力状态的标志,也是棕色和米色/明亮脂肪细胞对产热活性适应性调节作出反应的标志。UCP1基因的5'非编码区包含赋予UCP1基因转录组织特异性、分化依赖性和神经激素调节的调控元件。两个主要区域——一个远端增强子和一个近端启动子区域——通过与大量转录因子相互作用来介导转录调控,这些转录因子包括核激素受体和cAMP反应性转录因子。共调节因子,如PGC-1α,在UCP1基因转录的协同调节中起关键作用。转录因子和共调节因子在UCP1基因启动子区域的多重相互作用导致局部染色质重塑,从而导致RNA聚合酶II的激活和可及性增加以及随后的基因转录。此外,UCP1基因增强子附近常见的A到G多态性影响UCP1基因转录的程度。值得注意的是,据报道肥胖及相关代谢疾病的特定方面与该位点的人类群体变异性有关。另一方面,UCP1启动子区域的独特特性已被用于开发用于实验目的的棕色脂肪组织特异性基因递送工具。