2010/01/07 by Yong Xu, Thusanth Thuraisingam, David Anderson de Lima Morais +2 · 2 citations
Biochemistry, Genetics and Molecular Biology · #Cellular Mechanics and Interactions #RNA Research and Splicing #Molecular Biology Techniques and Applications #Biology #Cell biology #Chromatin immunoprecipitation #Transactivation #Actin #Molecular biology #Gene knockdown #Cell nucleus #Gene expression #Signal transduction #Regulation of gene expression #Gene #Cytoplasm #Promoter #Genetics
paper · doi:10.1091/mbc.e09-06-0534
openalex publication_date 2010/01/07 · openalex created_date 2025/10/10 · openalex updated_date 2026/08/01
Studies have shown that nuclear translocation of actin occurs under certain conditions of cellular stress; however, the functional significance of actin import remains unclear. Here, we demonstrate that during the phorbol 12-myristate 13-acetate (PMA)-induced differentiation of HL-60 cells toward macrophages, beta-actin translocates from the cytoplasm to the nucleus and that this process is dramatically inhibited by pretreatment with p38 mitogen-activated protein kinase inhibitors. Using chromatin immunoprecipitation-on-chip assays, the genome-wide maps of beta-actin binding to gene promoters in response to PMA treatment is analyzed in HL-60 cells. A gene ontology-based analysis shows that the identified genes belong to a broad spectrum of functional categories such as cell growth and differentiation, signal transduction, response to external stimulus, ion channel activity, and immune response. We also demonstrate a correlation between beta-actin occupancy and the recruitment of RNA polymerase II at six selected target genes, and beta-actin knockdown decreases the mRNA expression levels of these target genes induced by PMA. We further show that nuclear beta-actin is required for PMA-induced transactivation of one target gene, solute carrier family 11 member 1, which is important for macrophage activation. Our data provide novel evidence that nuclear accumulation of beta-actin is involved in transcriptional regulation during macrophage-like differentiation of HL-60 cells.