Journal: bioRxiv
Article Title: Discovery of a tRNA-regulatory transcription factor that suppresses breast cancer metastasis
doi: 10.1101/2025.04.26.650725
Figure Lengend Snippet: (A) Pulldown immunoprecipitation (IP) results demonstrating interactions between ZZEF1 domains and mononucleosomes. In, input. IP, biotin pulldown. His, anti-His-tag western blot. (B) Dot plot showing CHD6 as a top interactor identified through ZZEF1 co-IP/MS. (C) Normalized ChIP-seq tracks showing enriched CHD6 binding (orange) in the proximal regions of tRNA-Lys-TTT-3 loci using a CHD6-specific antibody, compared to an IgG control in MDA cells. The purple tracks represent ZZEF1 binding from . (D) Normalized ATAC-seq tracks showing chromatin accessibility at tRNA-Lys-TTT-3 loci in MDA cells with ZZEF1 knockdown, CHD6 knockdown, and CHD6 knockdown in a ZZEF1-deficient background, compared to control cells. (E) Boxplot showing statistical analysis of chromatin accessibility from ATAC-seq at the tRNA-Lys-TTT-3 loci and non-target loci in ZZEF1 knockdown, CHD6 knockdown, and CHD6 knockdown in a ZZEF1-deficient background compared to control cells.
Article Snippet: E. coli codon-optimized DNA sequences coding ZZEF1 domains (EF hand (111-146 amino acid), DOC (226-405 amino acid), ZZ1 (1778-1833 amino acid), ZZ2 (1827-1882 amino acid), ZZ1/2 (1778-1882 amino acid)) were synthesized and cloned into a His-MBP fusion expression vector (Addgene #29654) via BamHI site and Gibson assembly.
Techniques: Immunoprecipitation, Western Blot, Co-Immunoprecipitation Assay, ChIP-sequencing, Binding Assay, Control, Knockdown