Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Hum Mutat. 2022 Dec;43(12):2033-2053. doi: 10.1002/humu.24461. Epub 2022 Sep 24.
Xia-Gibbs syndrome (XGS; MIM# 615829) is a rare mendelian disorder characterized by Development Delay (DD), intellectual disability (ID), and hypotonia. Individuals with XGS typically harbor de novo protein-truncating mutations in the AT-Hook DNA binding motif containing 1 (AHDC1) gene, although some missense mutations can also cause XGS. Large de novo heterozygous deletions that encompass the AHDC1 gene have also been ascribed as diagnostic for the disorder, without substantial evidence to support their pathogenicity. We analyzed 19 individuals with large contiguous deletions involving AHDC1, along with other genes. One individual bore the smallest known contiguous AHDC1 deletion (∼350 Kb), encompassing eight other genes within chr1p36.11 (Feline Gardner-Rasheed, IFI6, FAM76A, STX12, PPP1R8, THEMIS2, RPA2, SMPDL3B) and terminating within the first intron of AHDC1. The breakpoint junctions and phase of the deletion were identified using both short and long read sequencing (Oxford Nanopore). Quantification of RNA expression patterns in whole blood revealed that AHDC1 exhibited a mono-allelic expression pattern with no deficiency in overall AHDC1 expression levels, in contrast to the other deleted genes, which exhibited a 50% reduction in mRNA expression. These results suggest that AHDC1 expression in this individual is compensated by a novel regulatory mechanism and advances understanding of mutational and regulatory mechanisms in neurodevelopmental disorders.
夏-吉布斯综合征(XGS;MIM# 615829)是一种罕见的孟德尔疾病,其特征为发育迟缓(DD)、智力残疾(ID)和低张力。XGS 患者通常存在 AT-Hook DNA 结合基序含 1 区(AHDC1)基因的新生截短突变,尽管一些错义突变也可导致 XGS。包含 AHDC1 基因的大型新生杂合性缺失也被认为是该疾病的诊断标准,但没有充分的证据支持其致病性。我们分析了 19 名患有涉及 AHDC1 基因的大片段连续缺失的个体,以及其他基因。一名个体携带了已知最小的连续 AHDC1 缺失(约 350Kb),包含 chr1p36.11 上的另外八个基因(Feline Gardner-Rasheed、IFI6、FAM76A、STX12、PPP1R8、THEMIS2、RPA2、SMPDL3B),并在 AHDC1 的第一个内含子内终止。使用短读和长读测序(Oxford Nanopore)确定了缺失的断点连接和相位。全血中 RNA 表达模式的定量分析表明,AHDC1 表现出单等位基因表达模式,总体上 AHDC1 表达水平没有缺陷,与其他缺失的基因形成对比,后者的 mRNA 表达水平降低了 50%。这些结果表明,该个体中 AHDC1 的表达通过一种新的调节机制得到代偿,并增进了对神经发育障碍中突变和调节机制的理解。