Structural rearrangements as a recurrent pathogenic mechanism for SETBP1haploinsufficiency

Autor: Alesi, V., Genovese, S., Roberti, M. C., Sallicandro, E., Di Tommaso, S., Loddo, S., Orlando, V., Pompili, D., Calacci, C., Mei, V., Pisaneschi, E., Faggiano, M. V., Morgia, A., Mammì, C., Astrea, G., Battini, R., Priolo, M., Dentici, M. L., Milone, R., Novelli, A.
Zdroj: Human Genomics; December 2024, Vol. 18 Issue: 1
Abstrakt: Chromosomal structural rearrangements consist of anomalies in genomic architecture that may or may not be associated with genetic material gain and loss. Evaluating the precise breakpoint is crucial from a diagnostic point of view, highlighting possible gene disruption and addressing to appropriate genotype–phenotype association. Structural rearrangements can either occur randomly within the genome or present with a recurrence, mainly due to peculiar genomic features of the surrounding regions. We report about three non-related individuals, harboring chromosomal structural rearrangements interrupting SETBP1, leading to gene haploinsufficiency. Two out of them resulted negative to Chromosomal Microarray Analysis (CMA), being the rearrangement balanced at a microarray resolution. The third one, presenting with a complex three-chromosome rearrangement, had been previously diagnosed with SETBP1haploinsufficiency due to a partial gene deletion at one of the chromosomal breakpoints. We thoroughly characterized the rearrangements by means of Optical Genome Mapping (OGM) and Whole Genome Sequencing (WGS), providing details about the involved sequences and the underlying mechanisms. We propose structural variants as a recurrent event in SETBP1haploinsufficiency, which may be overlooked by laboratory routine genomic analyses (CMA and Whole Exome Sequencing) or only partially determined when associated with genomic losses at breakpoints. We finally introduce a possible role of SETBP1in a Noonan-like phenotype.
Databáze: Supplemental Index
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