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Identification of biallelic mutations in MCM3AP and comprehensive literature analysis
被引:0
|作者:
Liu, Chan
[1
,2
]
Xie, Qingfeng
[1
,2
]
Hu, Quan
[1
,2
]
Xiang, Bingwu
[1
,2
]
Zhao, Kaiyi
[1
,2
]
Chen, Xiang
[1
,2
]
Zheng, Feixia
[2
,3
]
机构:
[1] Wenzhou Med Univ, Affiliated Hosp 2, Dept Phys Med & Rehabil Ctr, Wenzhou, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou, Zhejiang, Peoples R China
[3] Wenzhou Med Univ, Affiliated Hosp, Dept Pediat Neurol, Wenzhou, Zhejiang, Peoples R China
关键词:
peripheral neuropathy;
intellectual disability;
MCM3AP;
GANP;
biallelic mutations;
DNA-REPLICATION;
ASSOCIATION;
INITIATION;
VARIANTS;
PROMOTES;
COMPLEX;
FAMILY;
SAC3;
D O I:
10.3389/fgene.2024.1405644
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Background: Minichromosome maintenance complex component 3 associated protein (MCM3AP) is a gene in which mutations can result in autosomal recessive peripheral neuropathy with or without impaired intellectual development. The MCM3AP genotype-phenotype correlation and prognosis remain unclear. The aim of this study was to explore the genotype-phenotype correlations pertaining to MCM3AP. Methods: Whole-exome sequencing (WES) combined with copy number variation sequencing (CNV-seq) were performed on the genomic DNA isolated from a Chinese family, and Sanger sequencing, quantitative PCR and cDNA analyses were performed to examine the mutations. The retrospective study was conducted on 28 individuals with biallelic MCM3AP mutation-related diseases, including features such as mutations, motor development impairment, intellectual disability, weakness/atrophy, and cerebral magnetic resonance imaging abnormalities. Results: Sequencing identified novel compound heterozygous mutations in MCM3AP, namely, a paternal variant c.1_5426del (loss of exons 1-25) and a maternal splicing variant c.1858 + 3A>G. Functional studies revealed that the variant c.1858 + 3A>G resulted in the heterozygous deletion of exon 5, thereby affecting splicing functionality. Furthermore, the compound heterozygous mutation may affect the functionality of the protein domain. Retrospective analysis revealed different genotype-phenotype correlations for the pathogenic variants in biallelic MCM3AP: all individuals (100%) with mutations outside the Sac3 domain exhibited early-onset symptoms, motor developmental delays, and cognitive abnormalities, conversely, the proportions of individuals carrying mutations within the domain were 26.7% (motor delays) and 46.7% (cognitive abnormalities). Conclusion: Our findings further expand the genetic mutation spectrum of biallelic MCM3AP and highlight the genotype-phenotype associations. Additionally, we elaborate on the importance of rehabilitation intervention.
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