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Endocrinology, Northwestern University"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJNA789183"],"scientific_name":["Mus musculus"],"long_description":["Using mRNA-seq and ChIP-seq in muscle tissue, we found that BCL6 controls a broad range of anabolic targets, directly suppressing eukaryotic translation initiation factor 4E-binding protein 1 (Eif4epb1) and myostatin (Mstn) while enhancing insulin-like growth factor 1 (Igf1) and androgen receptor (Ar). Consistent with these gene regulatory effects, skeletal muscle ablation of Bcl6 increased physical association of the translation initiation factor eIF4E with its inhibitor EIF4E-BP1 and ribosomal sequencing in vivo revealed reduced translation efficiency. Overall design: Genome-wide maps of chromatin state, gene expression, and translation efficiency in skeletal muscle in wild-type, control, and Bcl6 knock-out mice."],"tag":["xref:PubMed:38337096"],"repository":["ENA"],"additional_accession":[]},"is_claimable":false,"name":"Translational control of skeletal muscle mass by the transcriptional repressor BCL6","description":"Translational control of skeletal muscle mass by the transcriptional repressor BCL6","dates":{"last_updated":"2025-09-24","first_public":"2023-12-27"},"accession":"PRJNA789183","cross_references":{"GEO":["GSE190956"],"taxon":["10090"],"PubMed":["38337096"]}}