Cassinari Kevin, Brehin Anne Claire, Kundul Ferdi, Castelain Mathieu, Patrier-Sallebert Sophie, Diguet Alain, Verspyck Eric, Houdayer Claude, Joly-Hélas Géraldine, Chambon Pascal
Department of Genetics and Reference Center for Developmental Disorders Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, 76000, Rouen, France.
Department of Pathology, Normandy Centre for Genomic and Personalized Medicine, Normandie University, UNIROUEN, U1245 and Rouen University Hospital, 76000, Rouen, Inserm, France.
Chromosome Res. 2025 Mar 12;33(1):3. doi: 10.1007/s10577-025-09763-5.
Jumping translocations and jumping-like translocations constitute a rare category of complex chromosomal rearrangements, which are primarily observed in hematologic disorders and solid tumors. This study outlines a complex structural mosaic rearrangement involving a single recipient chromosome and three distinct donor chromosomes, with varying patterns of mosaicism observed across different cell lines. The rearrangement was confirmed by karyotyping, FISH, and array-CGH. These analyses revealed significant chromosomal duplications and deletions, which may contribute to the observed phenotypic abnormalities. Following characterization via various cytogenetic techniques, this rearrangement appears to be the first reported instance of a jumping-like translocation in prenatal constitutional genetics. This finding enables the formulation of hypotheses regarding the mechanisms underlying such intricate structural variants and their detection via contemporary genetic methods.
跳跃性易位和类跳跃性易位构成了一类罕见的复杂染色体重排,主要见于血液系统疾病和实体瘤。本研究概述了一种涉及一条受体染色体和三条不同供体染色体的复杂结构嵌合重排,在不同细胞系中观察到了不同的嵌合模式。通过核型分析、荧光原位杂交(FISH)和阵列比较基因组杂交(array-CGH)证实了这种重排。这些分析揭示了明显的染色体重复和缺失,这可能导致了观察到的表型异常。通过各种细胞遗传学技术进行特征描述后,这种重排似乎是产前体质遗传学中首次报道的类跳跃性易位实例。这一发现有助于就此类复杂结构变异的潜在机制及其通过当代遗传方法的检测提出假设。