Mutations in OOEP and NLRP5 identified in infertile patients with early embryonic arrest,Human Mutation

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Mutations in OOEP and NLRP5 identified in infertile patients with early embryonic arrest
Human Mutation ( IF 3.9 ) Pub Date : 2022-08-10 , DOI: 10.1002/humu.24448
Xiaomei Tong _{1,

2} , Jiamin Jin _{1,

2} , Zhanhong Hu _{1,

2} , Yingyi Zhang _{1,

2} , Heng-Yu Fan _{2,

3} , Yin-Li Zhang _{1,

2} , Songying Zhang _{1,

2}

Affiliation

The subcortical maternal complex (SCMC), composed of several maternal-effect genes, is vital for the development of oocytes and early embryos. Variants of SCMC-encoding genes (NLRP2, NLRP5, TLE6, PADI6, and KHDC3L, but not OOEP and ZBED3) are associated with human oocyte maturation dysfunction, fertilization failure, and early embryonic arrest. In this study, we enrolled 118 Chinese patients who experienced recurrent preimplantation embryonic arrest during assisted reproductive technology treatments and performed whole-exome sequencing. We discovered compound heterozygous missense variants (c.110G>C and c.109C>G) in the OOEP gene in one patient who experienced recurrent preimplantation embryonic arrest. Arrested embryos from this affected patient were analyzed by single-cell RNA sequencing, which showed a downregulated transcriptome. In addition, six novel NLRP5 variants (c.971T>A, c.3341T>C, c.1575_1576delAG, c.1830_1831delGT, c.1202C>T, and c.2378T>G) were identified in four patients with arrested and severely fragmented embryos. These suspicious mutations were examined by in vitro studies in HEK293T cells. Western blot analysis and immunofluorescence experiments showed that OOEP and partial NLRP5 mutations caused decreased protein levels. Our findings first demonstrated that biallelic variants in OOEP gene could also cause human early embryonic arrest, similar to other SCMC components. We expanded the genetic mutation spectrum of SCMC genes related to early embryogenesis in humans, especially early embryonic arrest.

更新日期：2022-08-10

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