Tejedor Juan Ramón, Soriano-Sexto Alejandro, Beccari Leonardo, Castejón-Fernández Natalia, Correcher Patricia, Sainz-Ledo Lidia, Alba-Linares Juan José, Urdinguio Rocío G, Ugarte Magdalena, Fernández Agustín F, Rodríguez-Pombo Pilar, Fraga Mario F, Pérez Belén
Nanomaterials and Nanotechnology Research Centre (CINN-CSIC), Spanish National Research Council (CSIC), Principality of Asturias, Spain.
Health Research Institute of Asturias (ISPA), Foundation for Biomedical Research and Innovation in Asturias (FINBA), Principality of Asturias, Spain.
J Inherit Metab Dis. 2025 Jan;48(1):e12829. doi: 10.1002/jimd.12829. Epub 2024 Dec 10.
Maple syrup urine disease (MSUD) is a rare inherited metabolic disorder characterized by deficient activity of the branched-chain alpha-ketoacid dehydrogenase (BCKDH) complex, required to metabolize the amino acids leucine, isoleucine, and valine. Despite its profound metabolic implications, the molecular alterations underlying this metabolic impairment had not yet been completely elucidated. We performed a comprehensive multi-omics integration analysis, including genomic, epigenomic, and transcriptomic data from fibroblasts derived from a cohort of MSUD patients and unaffected controls to genetically characterize an MSUD case and to unravel the MSUD pathophysiology. MSUD patients exhibit a defined episignature that reshapes the global DNA methylation landscape, resulting in the stimulation of HOX cluster genes and the restriction of cell cycle gene-related signatures. Subsequent data integration revealed the impact of AP1-related and CEBPB transcription factors on the observed molecular reorganization, with MEIS1 emerging as a potential downstream candidate affected by robust epigenetic repression in MSUD patients. Furthermore, the integration of multi-omics layers facilitated the identification of a strong epigenetic repression in the DBT promoter in a patient wherein no BCKDH pathogenic variants had been detected. A Circular Chromatin Conformation Capture assay indicated a disturbance of the interactions of DBT promoter, thereby unveiling alternative modes of disease inheritance. Integration of multi-omics data unveiled underlying molecular networks rewired in MSUD patients and represents a powerful approach with diagnostic potential for rare genetic disorders with unknown genetic bases.
枫糖尿症(MSUD)是一种罕见的遗传性代谢紊乱疾病,其特征是代谢亮氨酸、异亮氨酸和缬氨酸所需的支链α-酮酸脱氢酶(BCKDH)复合体活性不足。尽管其具有深远的代谢影响,但这种代谢损伤背后的分子改变尚未完全阐明。我们进行了全面的多组学整合分析,包括来自一组MSUD患者和未受影响对照的成纤维细胞的基因组、表观基因组和转录组数据,以对一个MSUD病例进行基因特征分析,并揭示MSUD的病理生理学机制。MSUD患者表现出一种特定的表观特征,重塑了整体DNA甲基化格局,导致HOX簇基因的激活和细胞周期基因相关特征的受限。随后的数据整合揭示了AP1相关和CEBPB转录因子对观察到的分子重组的影响,MEIS1作为MSUD患者中受强烈表观遗传抑制影响的潜在下游候选基因出现。此外,多组学层面的整合有助于在一名未检测到BCKDH致病变异的患者中鉴定出DBT启动子中的强烈表观遗传抑制。环状染色质构象捕获分析表明DBT启动子的相互作用受到干扰,从而揭示了疾病遗传的替代模式。多组学数据的整合揭示了MSUD患者中重新连接的潜在分子网络,代表了一种对具有未知遗传基础的罕见遗传疾病具有诊断潜力的强大方法。