Division of Human Genetics, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45215, USA.
Center for Cancer and Cell Biology, Van Andel Institute, Grand Rapids, MI 49503, USA.
Development. 2023 Feb 1;150(3). doi: 10.1242/dev.201038. Epub 2023 Feb 15.
Frizzled 2 (FZD2) is a transmembrane Wnt receptor. We previously identified a pathogenic human FZD2 variant in individuals with FZD2-associated autosomal dominant Robinow syndrome. The variant encoded a protein with a premature stop and loss of 17 amino acids, including a region of the consensus dishevelled-binding sequence. To model this variant, we used zygote microinjection and i-GONAD-based CRISPR/Cas9-mediated genome editing to generate a mouse allelic series. Embryos mosaic for humanized Fzd2W553* knock-in exhibited cleft palate and shortened limbs, consistent with patient phenotypes. We also generated two germline mouse alleles with small deletions: Fzd2D3 and Fzd2D4. Homozygotes for each allele exhibit a highly penetrant cleft palate phenotype, shortened limbs compared with wild type and perinatal lethality. Fzd2D4 craniofacial tissues indicated decreased canonical Wnt signaling. In utero treatment with IIIC3a (a DKK inhibitor) normalized the limb lengths in Fzd2D4 homozygotes. The in vivo replication represents an approach for further investigating the mechanism of FZD2 phenotypes and demonstrates the utility of CRISPR knock-in mice as a tool for investigating the pathogenicity of human genetic variants. We also present evidence for a potential therapeutic intervention.
卷曲蛋白 2(FZD2)是一种跨膜 Wnt 受体。我们之前在患有 FZD2 相关常染色体显性罗宾诺综合征的个体中鉴定出一种致病性的人类 FZD2 变体。该变体编码的蛋白质含有一个过早的停止和 17 个氨基酸的缺失,包括一个公认的离散结合序列区域。为了模拟这种变体,我们使用受精卵微注射和基于 i-GONAD 的 CRISPR/Cas9 介导的基因组编辑来产生一系列具有人类化 Fzd2W553* 敲入的小鼠等位基因。胚胎镶嵌具有人类化 Fzd2W553* 敲入的个体表现出腭裂和肢体缩短,与患者表型一致。我们还生成了两个具有小缺失的生殖系小鼠等位基因:Fzd2D3 和 Fzd2D4。每个等位基因的纯合子都表现出高度穿透性的腭裂表型,与野生型相比,肢体缩短,并伴有围产期致死性。Fzd2D4 颅面组织显示出减少的经典 Wnt 信号。在体内用 IIIC3a(一种 DKK 抑制剂)处理可使 Fzd2D4 纯合子的肢体长度正常化。体内复制代表了进一步研究 FZD2 表型机制的方法,并证明了 CRISPR 敲入小鼠作为研究人类遗传变异致病性的工具的实用性。我们还提供了潜在治疗干预的证据。