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.
引用
收藏
页数:10
相关论文
共 50 条
  • [41] Primary hepatocellular adenoma due to biallelic HNF1A mutations and its co-occurrence with MODY 3: case-report and review of the literature
    Junling Fu
    Tong Wang
    Xiao Zhai
    Xinhua Xiao
    Endocrine, 2020, 67 : 544 - 551
  • [42] Identification of Data Analysis Methods and Focus Trends in Port State Control Inspections: A Comprehensive Literature Review
    Junaidi, Arif
    Yudo, Hartono
    Ab-Samat, Hasnida
    INTERNATIONAL JOURNAL OF TECHNOLOGY, 2024, 15 (01) : 179 - 194
  • [43] Identification and Proteomic Analysis of Distinct UBE3A/E6AP Protein Complexes
    Martinez-Noel, Gustavo
    Galligan, Jeffrey T.
    Sowa, Mathew E.
    Arndt, Verena
    Overton, Thomas M.
    Harper, J. Wade
    Howley, Peter M.
    MOLECULAR AND CELLULAR BIOLOGY, 2012, 32 (15) : 3095 - 3106
  • [44] Genome-Wide Identification and Comprehensive Analysis of the AP2/ERF Gene Family in Pomegranate Fruit Development and Postharvest Preservation
    Wan, Ran
    Song, Jinhui
    Lv, Zhenyang
    Qi, Xingcheng
    Han, Xuemeng
    Guo, Qiang
    Wang, Sa
    Shi, Jiangli
    Jian, Zaihai
    Hu, Qingxia
    Chen, Yanhui
    GENES, 2022, 13 (05)
  • [45] A comprehensive literature review and meta-analysis of the prevalence of pan-cancer BRCA mutations, homologous recombination repair gene mutations, and homologous recombination deficiencies
    Shao, Changxia
    Wan, Jun
    Lam, Fred C.
    Tang, Huilin
    Marley, Andrew R.
    Song, Yiqing
    Miller, Chelsey
    Brown, Madeline
    Han, Jiali
    Adeboyeje, Gboyega
    ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 2022, 63 (06) : 308 - 316
  • [46] Identification of mutations in HPRP3, the gene for autosomal dominant retinitis pigmentosa on chromosome 1 and functional analysis of mutations
    Vithana, EN
    Chakarova, CF
    Bolz, H
    Safieh, LA
    Wilkie, S
    Moore, AT
    Gal, A
    Bird, AC
    Hunt, DM
    Bhattacharya, SS
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2002, 43 : U169 - U169
  • [47] Genetic analysis of developmental and epileptic encephalopathy caused by novel biallelic SZT2 gene mutations in three Chinese Han infants: a case series and literature review
    Yang, Sai
    Yang, Li-Ming
    Liao, Hong-Mei
    Fang, Hong-Jun
    Ning, Ze-Shu
    Liao, Cai-Shi
    Wu, Li-Wen
    NEUROLOGICAL SCIENCES, 2022, 43 (08) : 5039 - 5048
  • [48] Genetic analysis of developmental and epileptic encephalopathy caused by novel biallelic SZT2 gene mutations in three Chinese Han infants: a case series and literature review
    Sai Yang
    Li-Ming Yang
    Hong-Mei Liao
    Hong-Jun Fang
    Ze-Shu Ning
    Cai-Shi Liao
    Li-Wen Wu
    Neurological Sciences, 2022, 43 : 5039 - 5048
  • [49] Comprehensive analysis of oncogenic effects of PIK3CA mutations in human mammary epithelial cells
    Zhang, Haijun
    Liu, Gang
    Dziubinski, Michele
    Yang, Zengquan
    Ethier, Stephen P.
    Wu, Guojun
    BREAST CANCER RESEARCH AND TREATMENT, 2008, 112 (02) : 217 - 227
  • [50] Comprehensive analysis of oncogenic effects of PIK3CA mutations in human mammary epithelial cells
    Haijun Zhang
    Gang Liu
    Michele Dziubinski
    Zengquan Yang
    Stephen P. Ethier
    Guojun Wu
    Breast Cancer Research and Treatment, 2008, 112 : 217 - 227