Open AccessWt1 directs the lineage specification of sertoli and granulosa cells by repressing Sf1 expression
Author(s) -
Min Chen,
Lianjun Zhang,
Xiuhong Cui,
Xiwen Lin,
Yaqiong Li,
Yaqing Wang,
Han Li,
Yan Qin,
Dahua Chen,
Chunsheng Han,
Bin Zhou,
Vicki Huff,
Fei Gao
Publication year - 2016
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.144105
Subject(s) - biology , sertoli cell , steroidogenic factor 1 , somatic cell , gonad , ectopic expression , sox9 , microbiology and biotechnology , gonadal ridge , embryonic stem cell , ovary , granulosa cell , sexual differentiation , medicine , endocrinology , cell culture , embryogenesis , gene expression , transcription factor , embryo , nuclear receptor , genetics , gene , spermatogenesis
Supporting cells (Sertoli and granulosa) and steroidogenic cells (Leydig and theca-interstitium) are two major somatic cell types in mammalian gonads. However, the mechanisms that control their differentiation during gonad development remain elusive. In this study, we found deletion of Wt1 in ovary after sex determination caused ectopic development of steroidogenic cells at embryonic stage. Furthermore, the differentiation of both Sertoli and granulosa cells was blocked when Wt1 was deleted before sex determination and most genital ridge somatic cells differentiated into steroidogenic cells in both male and female gonads. Further studies revealed WT1 repressed Sf1 expression by directly binding to the Sf1 promoter region, and the repressive function was completely abolished when WT1 binding sites were mutated. This study demonstrated Wt1 is required for the lineage specification of both Sertoli and granulosa cells by repressing Sf1 expression. Without Wt1, the expression of Sf1 was upregulated and the somatic cells differentiated into steroidogenic cells instead of supporting cells. Our study uncovered a novel mechanism of somatic cell differentiation during gonad development.