Human Genome and Stem-Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil.
The Federal Research Center Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.
Chromosome Res. 2024 Mar 19;32(2):6. doi: 10.1007/s10577-024-09750-2.
Structural variants (SVs) pose a challenge to detect and interpret, but their study provides novel biological insights and molecular diagnosis underlying rare diseases. The aim of this study was to resolve a 9p24 rearrangement segregating in a family through five generations with a congenital heart defect (congenital pulmonary and aortic valvular stenosis and pulmonary artery stenosis), by applying a combined genomic analysis. The analysis involved multiple techniques, including karyotype, chromosomal microarray analysis (CMA), FISH, genome sequencing (GS), RNA-seq, and optical genome mapping (OGM). A complex 9p24 SV was hinted at by CMA results, showing three interspersed duplicated segments. Combined GS and OGM analyses revealed that the 9p24 duplications constitute a complex SV, on which a set of breakpoints matches the boundaries of the CMA duplicated sequences. The proposed structure for this complex rearrangement implies three duplications associated with an inversion of ~ 2 Mb region on chromosome 9 and a SINE element insertion at the more distal breakpoint. Interestingly, this genomic structure of rearrangement forms a chimeric transcript of the KANK1/DMRT1 loci, which was confirmed by both RNA-seq and Sanger sequencing on blood samples from 9p24 rearrangement carriers. Altogether with breakpoint amplification and FISH analysis, this combined approach allowed a deep characterization of this complex rearrangement. Although the genotype-phenotype correlation remains elusive from the molecular mechanism point of view, this study identified a large genomic rearrangement at 9p24 segregating with a familial congenital heart defect, revealing a genetic biomarker that was successfully applied for embryo selection, changing the reproductive perspective of affected individuals.
结构变异(SVs)的检测和解释颇具挑战,但它们的研究为罕见疾病的新型生物学见解和分子诊断提供了依据。本研究的目的是通过应用基因组联合分析,解析一个家系中存在的 9p24 重排,该家系中存在 5 代人共有的先天性心脏缺陷(先天性肺和主动脉瓣狭窄及肺动脉狭窄)。该分析涉及多种技术,包括核型分析、染色体微阵列分析(CMA)、荧光原位杂交(FISH)、基因组测序(GS)、RNA-seq 和光学基因组图谱(OGM)。CMA 结果提示存在复杂的 9p24 SV,显示三个散布的重复片段。联合 GS 和 OGM 分析显示,9p24 重复构成了一个复杂的 SV,其一系列断点与 CMA 重复序列的边界相匹配。该复杂重排的提出结构表明,三个重复与染色体 9 上约 2 Mb 区域的倒位以及更远端断点处的 SINE 元件插入有关。有趣的是,这种重排的基因组结构形成了 KANK1/DMRT1 基因座的嵌合转录本,这在 9p24 重排携带者的血液样本的 RNA-seq 和 Sanger 测序中均得到了证实。综合断点扩增和 FISH 分析,这种联合方法能够对这种复杂重排进行深入的特征描述。尽管从分子机制的角度来看,基因型-表型相关性仍然难以捉摸,但本研究在 9p24 上鉴定出与家族性先天性心脏缺陷相关的大型基因组重排,揭示了一种遗传生物标志物,该标志物已成功应用于胚胎选择,改变了受影响个体的生殖前景。