Wdr62 is involved in female meiotic initiation via activating JNK signaling and associated with POI in humans.
Yang ZhouYan QinYingying QinBinyang XuTing GuoHanni KeMin ChenLianjun ZhangFeng HanYaqiong LiMin ChenAxel BehrensYaqing WangZhiheng XuZi-Jiang ChenFei GaoPublished in: PLoS genetics (2018)
Meiosis is a germ cell-specific division that is indispensable for the generation of haploid gametes. However, the regulatory mechanisms of meiotic initiation remain elusive. Here, we report that the Wdr62 (WD40-repeat protein 62) is involved in meiotic initiation as a permissive factor rather than an instructive factor. Knock-out of this gene in a mouse model resulted in female meiotic initiation defects. Further studies demonstrated that Wdr62 is required for RA-induced Stra8 expression via the activation of JNK signaling, and the defects in meiotic initiation from Wdr62-deficient female mice could be partially rescued by JNK1 overexpression in germ cells. More importantly, two novel mutations of the WDR62 gene were detected in patients with premature ovarian insufficiency (POI), and these mutations played dominant-negative roles in regulating Stra8 expression. Hence, this study revealed that Wdr62 is involved in female meiotic initiation via activating JNK signaling, which displays a novel mechanism for regulating meiotic initiation, and mutation of WDR62 is one of the potential etiologies of POI in humans.
Keyphrases
- signaling pathway
- induced apoptosis
- cell death
- mouse model
- poor prognosis
- endoplasmic reticulum stress
- transcription factor
- cell proliferation
- germ cell
- cell cycle arrest
- copy number
- type diabetes
- oxidative stress
- gene expression
- risk assessment
- metabolic syndrome
- single cell
- binding protein
- long non coding rna
- idiopathic pulmonary fibrosis
- disease activity
- high glucose
- genome wide identification
- human health
- systemic sclerosis