辅活化剂
过氧化物酶体增殖物激活受体
转录因子
PPARGC1A型
核受体
过氧化物酶体
核受体辅活化子2
生物
神经退行性变
细胞生物学
能量稳态
受体
内分泌学
内科学
生物化学
基因
医学
疾病
作者
Christoph Handschin,Bruce M. Spiegelman
出处
期刊:Endocrine Reviews
[The Endocrine Society]
日期:2006-10-03
卷期号:27 (7): 728-735
被引量:975
摘要
Many biological programs are regulated at the transcriptional level. This is generally achieved by the concerted actions of several transcription factors. Recent findings have shown that, in many cases, transcriptional coactivators coordinate the overall regulation of the biological programs. One of the best-studied examples of coactivator control of metabolic pathways is the peroxisome proliferator-activated receptor γ coactivator 1 (PGC-1) family. These proteins are strong activators of mitochondrial function and are thus dominant regulators of oxidative metabolism in a variety of tissues. The PGC-1 coactivators themselves are subject to powerful regulation at the transcriptional and posttranslational levels. Recent studies have elucidated the function of the PGC-1 coactivators in different tissues and have highlighted the implications of PGC-1 dysregulation in diseases such as diabetes, obesity, cardiomyopathy, or neurodegeneration.
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