Nishimura Naoto, Ueharu Hiroki, Nishihara Hiroto, Shibuya Shiori, Yoshida Saishu, Higuchi Masashi, Kanno Naoko, Horiguchi Kotaro, Kato Takako, Kato Yukio
Division of Life Science, Graduate School of Agriculture, Meiji University, Kanagawa 214-8571, Japan.
J Reprod Dev. 2016;62(1):93-102. doi: 10.1262/jrd.2015-092. Epub 2015 Dec 6.
Pituitary-specific transcription factor PROP1, a factor important for pituitary organogenesis, appears on rat embryonic day 11.5 (E11.5) in SOX2-expressing stem/progenitor cells and always coexists with SOX2 throughout life. PROP1-positive cells at one point occupy all cells in Rathke's pouch, followed by a rapid decrease in their number. Their regulatory factors, except for RBP-J, have not yet been clarified. This study aimed to use the 3 kb upstream region and 1st intron of mouse prop1 to pinpoint a group of factors selected on the basis of expression in the early pituitary gland for expression of Prop1. Reporter assays for SOX2 and RBP-J showed that the stem/progenitor marker SOX2 has cell type-dependent inhibitory and activating functions through the proximal and distal upstream regions of Prop1, respectively, while RBP-J had small regulatory activity in some cell lines. Reporter assays for another 39 factors using the 3 kb upstream regions in CHO cells ultimately revealed that 8 factors, MSX2, PAX6, PIT1, PITX1, PITX2, RPF1, SOX8 and SOX11, but not RBP-J, regulate Prop1 expression. Furthermore, a synergy effect with SOX2 was observed for an additional 10 factors, FOXJ1, HES1, HEY1, HEY2, KLF6, MSX1, RUNX1, TEAD2, YBX2 and ZFP36Ll, which did not show substantial independent action. Thus, we demonstrated 19 candidates, including SOX2, to be regulatory factors of Prop1 expression.
垂体特异性转录因子PROP1是垂体器官发生的重要因子,在大鼠胚胎第11.5天(E11.5)出现在表达SOX2的干/祖细胞中,并在整个生命过程中始终与SOX2共存。PROP1阳性细胞一度占据拉特克囊中的所有细胞,随后其数量迅速减少。除RBP-J外,其调控因子尚未明确。本研究旨在利用小鼠prop1的3 kb上游区域和第1内含子,找出一组基于早期垂体表达而筛选出的调控Prop1表达的因子。对SOX2和RBP-J的报告基因检测表明,干/祖细胞标志物SOX2分别通过Prop1的近端和远端上游区域具有细胞类型依赖性的抑制和激活功能,而RBP-J在某些细胞系中的调控活性较小。在CHO细胞中使用3 kb上游区域对另外39个因子进行报告基因检测,最终发现8个因子,即MSX2、PAX6、PIT1、PITX1、PITX2、RPF1、SOX8和SOX11,但不包括RBP-J,可调控Prop1的表达。此外,还观察到另外10个因子,即FOXJ1、HES1、HEY1、HEY2、KLF6、MSX1、RUNX1、TEAD2、YBX2和ZFP36Ll与SOX2存在协同效应,它们并未表现出显著的独立作用。因此,我们证明了包括SOX2在内的19个候选因子是Prop1表达的调控因子。