Division of Hematology, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Department of Epigenetics and Molecular Carcinogenesis, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Mol Cell. 2021 Jan 21;81(2):239-254.e8. doi: 10.1016/j.molcel.2020.11.006. Epub 2020 Dec 9.
Metazoan transcription factors typically regulate large numbers of genes. Here we identify via a CRISPR-Cas9 genetic screen ZNF410, a pentadactyl DNA-binding protein that in human erythroid cells directly activates only a single gene, the NuRD component CHD4. Specificity is conveyed by two highly evolutionarily conserved clusters of ZNF410 binding sites near the CHD4 gene with no counterparts elsewhere in the genome. Loss of ZNF410 in adult-type human erythroid cell culture systems and xenotransplantation settings diminishes CHD4 levels and derepresses the fetal hemoglobin genes. While previously known to be silenced by CHD4, the fetal globin genes are exposed here as among the most sensitive to reduced CHD4 levels.. In vitro DNA binding assays and crystallographic studies reveal the ZNF410-DNA binding mode. ZNF410 is a remarkably selective transcriptional activator in erythroid cells, and its perturbation might offer new opportunities for treatment of hemoglobinopathies.
后生动物转录因子通常调节大量基因。在这里,我们通过 CRISPR-Cas9 基因敲除筛选鉴定了一个五趾 DNA 结合蛋白 ZNF410,它在人类红细胞中仅直接激活单个基因,即 NuRD 成分 CHD4。特异性由 CHD4 基因附近两个高度进化保守的 ZNF410 结合位点簇传递,在基因组的其他地方没有相应的位点。在成人型人类红细胞培养系统和异种移植环境中,ZNF410 的缺失降低了 CHD4 水平并解除了胎儿血红蛋白基因的抑制。虽然先前已知被 CHD4 沉默,但这里暴露的胎儿球蛋白基因是对降低的 CHD4 水平最敏感的基因之一。体外 DNA 结合测定和晶体学研究揭示了 ZNF410-DNA 结合模式。ZNF410 是红细胞中一种非常选择性的转录激活剂,其干扰可能为血红蛋白病的治疗提供新的机会。