Analysis of three Chinese pedigrees affected with recurrent hydatidiform mole due to variants of NLRP7 gene.
10.3760/cma.j.cn511374-20220103-00001
- Author:
Jiandong SHEN
1
;
Yan GAO
;
Wei WU
;
Jinyong LIU
;
Xueping SUN
;
Yawen PENG
;
Jiazi XIE
;
Daowu WANG
;
Yugui CUI
;
Jiayin LIU
;
Feiyang DIAO
Author Information
1. Center of Reproductive Medicine, the First Affiliated Hospital of Nanjing Medical University, State Key Laboratory of Reproductive Medicine, Nanjing, Jiangsu 210029, China. phenix_y@163.com.
- Publication Type:Journal Article
- MeSH:
Adaptor Proteins, Signal Transducing/genetics*;
Aged;
China;
Female;
Homozygote;
Humans;
Hydatidiform Mole/pathology*;
Mutation;
Pedigree;
Pregnancy;
Sequence Deletion
- From:
Chinese Journal of Medical Genetics
2022;39(10):1070-1075
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the genetic etiology of recurrent hydatidiform mole (RHM) and provide accurate guidance for reproduction.
METHODS:Peripheral venous blood samples of the probands with RHM and members from 5 unrelated pedigrees were collected. Genomic DNA was extracted by using routine method, and whole exome sequencing was carried out to detect variants of RHM-associated genes including NLRP7 and KHDC3L. Sanger sequencing and real-time quantitative PCR (RT-qPCR) were used to validate the candidate variants and delineate their parental origin.
RESULTS:Homozygous or compound heterozygous variants of the NLRP7 gene were identified in four patients from three pedigrees, which included a homozygous deletion of exon 1 to 4 of NLRP7 in patient P1 and her elder sister, compound heterozygous variants of NLRP7 c.939delG (p.Q314Sfs*6) pat and c.1533delG (p.N512Tfs*4) mat in patient P2, and compound heterozygous variants of NLRP7 c.2389_2390delTC (p.A798Qfs*6) pat and c.2165A>G (p.D722G) mat in patient P4. All variants were interpreted as pathogenic or likely pathogenic according to the American College of Medical and Genomics (ACMG) guidelines. Among these, NLRP7 exons 1 to 4 deletion, c.939delG (p.Q314Sfs*6), c.1533delG (p.N512Tfs*4) and c.2389_2390delTC (p.A798Qfs*6) were unreported previously.
CONCLUSION:Variants of the NLRP7 gene probably underlay autosomal recessive RHM in the three pedigrees, and definitive molecular diagnosis is beneficial for accurate genetic counseling. Above finding has also enriched the spectrum of the NLRP7 variants underlying RHM.
