寻找垂体特异性转录因子PROP1基因的调控因子

Naoto Nishimura, Hiroki Ueharu, H. Nishihara, Shiori Shibuya, S. Yoshida, M. Higuchi, Naoko Kanno, K. Horiguchi, T. Kato, Y. Kato
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引用次数: 6

摘要

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)在表达SOX2的干/祖细胞中出现,并在一生中始终与SOX2共存。prop1阳性细胞一度占据Rathke 's袋内的所有细胞,随后其数量迅速减少。除RBP-J外,它们的调节因子尚未明确。本研究旨在利用小鼠prop1的上游3kb区域和第1内含子,确定在垂体早期表达基础上选择的一组影响prop1表达的因子。对SOX2和RBP-J的报告基因分析表明,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在某些细胞系中具有较小的调控活性。利用CHO细胞上游3kb区域对另外39个因子进行报告性分析,最终发现有8个因子(MSX2、PAX6、PIT1、PITX1、PITX2、RPF1、SOX8和SOX11)调控Prop1的表达,但不包括RBP-J。此外,FOXJ1、HES1、HEY1、HEY2、KLF6、MSX1、RUNX1、TEAD2、YBX2和ZFP36Ll等10个因子与SOX2存在协同作用,但未表现出明显的独立作用。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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Search for regulatory factors of the pituitary-specific transcription factor PROP1 gene
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.
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