| Literature DB >> 33859416 |
Divya S Vinjamur1, Qiuming Yao1,2, Mitchel A Cole1, Connor McGuckin1, Chunyan Ren1, Jing Zeng1, Mir Hossain1, Kevin Luk3, Scot A Wolfe3, Luca Pinello2, Daniel E Bauer4.
Abstract
Known fetal hemoglobin (HbF) silencers have potential on-target liabilities for rational β-hemoglobinopathy therapeutic inhibition. Here, through transcription factor (TF) CRISPR screening, we identify zinc-finger protein (ZNF) 410 as an HbF repressor. ZNF410 does not bind directly to the genes encoding γ-globins, but rather its chromatin occupancy is concentrated solely at CHD4, encoding the NuRD nucleosome remodeler, which is itself required for HbF repression. CHD4 has two ZNF410-bound regulatory elements with 27 combined ZNF410 binding motifs constituting unparalleled genomic clusters. These elements completely account for the effects of ZNF410 on fetal globin repression. Knockout of ZNF410 or its mouse homolog Zfp410 reduces CHD4 levels by 60%, enough to substantially de-repress HbF while eluding cellular or organismal toxicity. These studies suggest a potential target for HbF induction for β-hemoglobin disorders with a wide therapeutic index. More broadly, ZNF410 represents a special class of gene regulator, a conserved TF with singular devotion to regulation of a chromatin subcomplex.Entities:
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Year: 2021 PMID: 33859416 PMCID: PMC8180380 DOI: 10.1038/s41588-021-00843-w
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330