神经生长因子IB
生物
线粒体生物发生
细胞生物学
线粒体
核受体
基因表达
线粒体DNA
分子生物学
转录因子
基因表达调控
基因
遗传学
作者
Duco S. Koenis,Inkie J. A. Evers‐van Gogh,Pieter B. van Loenen,Wilbert Zwart,Eric Kalkhoven,Carlie J.M. de Vries
出处
期刊:FEBS Letters
[Wiley]
日期:2024-06-02
卷期号:598 (14): 1715-1729
标识
DOI:10.1002/1873-3468.14942
摘要
Mitochondrial biogenesis requires precise regulation of both mitochondrial‐encoded and nuclear‐encoded genes. Nuclear receptor Nur77 is known to regulate mitochondrial metabolism in macrophages and skeletal muscle. Here, we compared genome‐wide Nur77 binding site and target gene expression in these two cell types, which revealed conserved regulation of mitochondrial genes and enrichment of motifs for the transcription factor Yin‐Yang 1 (YY1). We show that Nur77 and YY1 interact, that YY1 increases Nur77 activity, and that their binding sites are co‐enriched at mitochondrial ribosomal protein gene loci in macrophages. Nur77 and YY1 co‐expression synergistically increases Mrpl1 expression as well as mitochondrial abundance and activity in macrophages but not skeletal muscle. As such, we identify a macrophage‐specific Nur77‐YY1 interaction that enhances mitochondrial metabolism.
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