Children's Hospital of Fudan University, Shanghai 201102, China.
Shanghai Key Laboratory of Birth Defects, Shanghai 201102, China.
Chin Med J (Engl). 2024 Aug 5;137(15):1823-1834. doi: 10.1097/CM9.0000000000003192. Epub 2024 Jul 8.
Heterotaxy (HTX) is a thoracoabdominal organ anomaly syndrome and commonly accompanied by congenital heart disease (CHD). The aim of this study was to analyze rare copy number variations (CNVs) in a HTX/CHD cohort and to examine the potential mechanisms contributing to HTX/CHD.
Chromosome microarray analysis was used to identify rare CNVs in a cohort of 120 unrelated HTX/CHD patients, and available samples from parents were used to confirm the inheritance pattern. Potential candidate genes in CNVs region were prioritized via the DECIPHER database, and PNPLA4 was identified as the leading candidate gene. To validate, we generated PNPLA4 -overexpressing human induced pluripotent stem cell lines as well as pnpla4 -overexpressing zebrafish model, followed by a series of transcriptomic, biochemical and cellular analyses.
Seventeen rare CNVs were identified in 15 of the 120 HTX/CHD patients (12.5%). Xp22.31 duplication was one of the inherited CNVs identified in this HTX/CHD cohort, and PNPLA4 in the Xp22.31 was a candidate gene associated with HTX/CHD. PNPLA4 is expressed in the lateral plate mesoderm, which is known to be critical for left/right embryonic patterning as well as cardiomyocyte differentiation, and in the neural crest cell lineage. Through a series of in vivo and in vitro analyses at the molecular and cellular levels, we revealed that the biological function of PNPLA4 is importantly involved in the primary cilia formation and function via its regulation of energy metabolism and mitochondria-mediated ATP production.
Our findings demonstrated a significant association between CNVs and HTX/CHD. Our data strongly suggested that an increased genetic dose of PNPLA4 due to Xp22.31 duplication is a disease-causing risk factor for HTX/CHD.
异构(HTX)是一种胸腹器官异常综合征,常伴有先天性心脏病(CHD)。本研究旨在分析 HTX/CHD 队列中的罕见拷贝数变异(CNVs),并探讨导致 HTX/CHD 的潜在机制。
采用染色体微阵列分析技术,对 120 例无亲缘关系的 HTX/CHD 患者进行罕见 CNVs 分析,并利用父母的可利用样本证实遗传模式。通过 DECIPHER 数据库对 CNVs 区域的潜在候选基因进行优先级排序,鉴定 PNPLA4 为主要候选基因。为了验证,我们生成了 PNPLA4 过表达的人类诱导多能干细胞系和 pnpla4 过表达的斑马鱼模型,随后进行了一系列转录组、生化和细胞分析。
在 120 例 HTX/CHD 患者中,有 15 例(12.5%)发现了 17 种罕见 CNVs。在这个 HTX/CHD 队列中,鉴定出 Xp22.31 重复是一种遗传 CNVs,Xp22.31 中的 PNPLA4 是与 HTX/CHD 相关的候选基因。PNPLA4 在侧中胚层表达,该组织对于左右胚胎模式以及心肌细胞分化至关重要,同时也在神经嵴细胞谱系中表达。通过一系列在分子和细胞水平上的体内和体外分析,我们揭示了 PNPLA4 通过调节能量代谢和线粒体介导的 ATP 产生,对初级纤毛的形成和功能具有重要的生物学功能。
我们的研究结果表明,CNVs 与 HTX/CHD 之间存在显著关联。我们的数据强烈表明,由于 Xp22.31 重复导致 PNPLA4 的遗传剂量增加是 HTX/CHD 的致病危险因素。