AIMP1负性调控PPARgamma:与脂肪形成有关

J. H. Kim, J. Han, Sunghoon Kim
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引用次数: 0

摘要

过氧化物酶体增殖物激活受体g (PPARg)作为脂肪形成的关键决定因素,其调控机制对于理解脂质代谢紊乱和糖代谢综合征的原因具有重要意义。在最近发表在《细胞科学杂志》上的一篇论文中,我们证明了氨基酰基- trna合成酶相互作用多功能蛋白1 (AIMP1)是一种新的ppar负调控因子。虽然AIMP1最初被发现是一个与多trna合成酶复合体相关的翻译因子,但它已被证明在多种细胞过程中发挥调节作用。现在AIMP1被证明通过与PPARg的dna结合域直接相互作用负调控PPARg介导的转录,抑制脂肪形成。这些结果表明,AIMP1作为一种新的PPARg抑制剂,提高了翻译与脂肪形成之间的可能联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
AIMP1 negatively regulates PPARgamma: Implication in adipogenesis
The regulation mechanism of peroxisome proliferator-activated receptor g (PPARg) known as key determinant in adipogenesis is important for understanding the cause of lipid metabolic disorders and glucose metabolic syndromes. In a recent paper published in Journal of Cell Science, we demonstrated that aminoacyl-tRNA synthetase-interacting multifunctional protein 1 (AIMP1) is a novel negative regulator of PPARg. Although AIMP1 is originally found as a factor associated with multi-tRNA synthetase complex for translation, it has been shown to play regulatory roles in diverse cellular processes. Now AIMP1 is shown to negatively regulates PPARg-mediated transcription through direct interaction with DNA-binding domain of PPARg and inhibits adipogenesis. These results suggest that AIMP1 functions as a novel inhibitor of PPARg, raising the possible linkage between translation and adipogenesis.
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