Khan Hammal, Koh Glenn, Chong Angie En Qi, Zahid Muhammad, Hussain Shabir, Ali Hamid, Ahmad Wasim, Xue Shifeng
Department of Biosciences, COMSATS University Islamabad, Islamabad, Pakistan.
Department of Biological Sciences, National University of Singapore, Singapore.
Clin Genet. 2023 Mar;103(3):341-345. doi: 10.1111/cge.14254. Epub 2022 Nov 1.
Isolated syndactyly is a common limb malformation with limited known genetic etiology. We used exome sequencing to discover a novel heterozygous missense variant c.2915G > C: p.Arg972Pro in AFF3 on chromosome 2q11.2 in a family with isolated syndactyly in hands and feet. AFF3 belongs to a family of nuclear transcription activating factors and is involved in limb dorsoventral patterning. The variant Arg972Pro is located near the C terminus, a region that is yet to be associated with human disorders. Functional studies did not show a difference in the stability or subcellular localization of the mutant and wild type proteins. Instead, overexpression in zebrafish embryos suggests that Arg972Pro is a loss-of-function allele. These results suggest that variants in the C terminus of AFF3 may cause a phenotype distinct from previously characterized AFF3 variants.
孤立性并指(趾)畸形是一种常见的肢体畸形,已知的遗传病因有限。我们利用外显子组测序,在一个患有手足孤立性并指(趾)畸形的家族中,发现了位于2号染色体q11.2上AFF3基因的一个新的杂合错义变异c.2915G>C:p.Arg972Pro。AFF3属于核转录激活因子家族,参与肢体背腹模式形成。变异体Arg972Pro位于C末端附近,该区域尚未与人类疾病相关联。功能研究未显示突变体和野生型蛋白质在稳定性或亚细胞定位上存在差异。相反,在斑马鱼胚胎中的过表达表明Arg972Pro是一个功能丧失等位基因。这些结果表明,AFF3基因C末端的变异可能导致与先前已鉴定的AFF3变异不同的表型。