Transcriptional coactivator PGC-1α contains a novel CBP80-binding motif that orchestrates efficient target gene expression.
Hana ChoXavier RamboutMichael L GleghornPhuong Quoc Thuc NguyenChristopher R PhippsKeita MiyoshiJason R MyersNaoyuki KataokaRudi FasanLynne E MaquatPublished in: Genes & development (2018)
Although peroxisome proliferator-activated receptor-γ (PPARγ) coactivator 1α (PGC-1α) is a well-established transcriptional coactivator for the metabolic adaptation of mammalian cells to diverse physiological stresses, the molecular mechanism by which it functions is incompletely understood. Here we used in vitro binding assays, X-ray crystallography, and immunoprecipitations of mouse myoblast cell lysates to define a previously unknown cap-binding protein 80 (CBP80)-binding motif (CBM) in the C terminus of PGC-1α. We show that the CBM, which consists of a nine-amino-acid α helix, is critical for the association of PGC-1α with CBP80 at the 5' cap of target transcripts. Results from RNA sequencing demonstrate that the PGC-1α CBM promotes RNA synthesis from promyogenic genes. Our findings reveal a new conduit between DNA-associated and RNA-associated proteins that functions in a cap-binding protein surveillance mechanism, without which efficient differentiation of myoblasts to myotubes fails to occur.
Keyphrases
- binding protein
- skeletal muscle
- gene expression
- single cell
- dna binding
- insulin resistance
- genome wide
- amino acid
- transcription factor
- dna methylation
- public health
- high resolution
- magnetic resonance imaging
- metabolic syndrome
- stem cells
- high throughput
- mesenchymal stem cells
- computed tomography
- adipose tissue
- cell free
- heat shock
- oxidative stress
- circulating tumor
- heat stress
- genome wide analysis