Open AccessDetection of TSC1 / TSC2 mosaic variants in patients with cardiac rhabdomyoma and tuberous sclerosis complex by hybrid‐capture next‐generation sequencing
Author(s) -
Wang Siyu,
Sun Hairui,
Wang Jianbin,
Gu Xiaoyan,
Han Lu,
Wu Yuduo,
Yan He,
Han Ling,
Zhang Hongjia,
He Yihua
Publication year - 2021
Publication title -
molecular genetics and genomic medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.765
H-Index - 29
ISSN - 2324-9269
DOI - 10.1002/mgg3.1802
Subject(s) - tuberous sclerosis , tsc1 , tsc2 , fetus , biology , multiplex ligation dependent probe amplification , digital polymerase chain reaction , multiplex , germline mosaicism , neurotypical , pathology , genetics , somatic cell , medicine , polymerase chain reaction , autism , pregnancy , exon , autism spectrum disorder , gene , apoptosis , pi3k/akt/mtor pathway , psychiatry
Background Fetal cardiac rhabdomyoma (CR) is strongly associated with tuberous sclerosis complex (TSC), which is caused by variants in TSC1 and TSC2 . However, in 10%–15% of patients with clinically confirmed TSC, no TSC1 / TSC2 variants are identified by panel sequencing or multiplex ligation‐dependent probe amplification (MLPA). Methods We analyzed eight fetuses with CR and their families. No TSC1 / TSC2 variants had previously been identified for six of these fetuses, and we suspected the other two families of gonadal mosaicism. We performed next‐generation sequencing (NGS) using CR tissue, umbilical cord tissue, and parental blood. All positive results, involving two paternal semen, were verified by droplet digital polymerase chain reaction (ddPCR). Results Four fetuses carried low‐level mosaic variants (0.05%–14.89%), and two only exhibited somatic mosaic variants in the CR tissue (15.76% and 37.69%). Two fathers had gonadal mosaicism (9.07% and 4.86%). We identified nine pathogenic variants in eight fetuses, including one fetus with a second‐hit variant. Conclusion The fetuses assessed in this study carried low ‐ level and somatic mosaic variants, and CR tissue from one fetus exhibited a second‐hit variant. Heterozygous gonadal variants can exist in patients with low‐level mosaicism. Combining NGS with ddPCR improves the accuracy of prenatal TSC diagnosis.