First Department of Pathology, Wakayama Medical University School of Medicine, 811-1 Kimiidera, Wakayama 641-0012, Japan.
Exp Mol Pathol. 2011 Apr;90(2):143-8. doi: 10.1016/j.yexmp.2010.11.010. Epub 2010 Nov 29.
Tricho-rhino-phalangeal syndrome (TRPS) is an autosomal dominant skeletal disorder caused by mutations of the Trps1 gene, which encodes a GATA type transcriptional repressor. To investigate the genes that act downstream of Trps1, we performed a DNA array using ATDC5 cells. One of the target genes identified from the DNA array was Runx1, which is essential for hematopoiesis and like Runx2 plays a significant role in chondrogenesis. A luciferase promoter assay and a chromosome immunoprecipitation assay showed that Runx1 expression in mouse epiphyseal cartilage was repressed by Trps1 binding to the GATA domain of the P2 promoter; the proximal segment of two promoters of the Runx1 gene. The aberrant expression of P2 transcripts was detected in growth plate chondrocytes from Trps1-null mice by in situ hybridization. In conclusion, Trps1 binds to the P2 promoter of the Runx1 gene and down-regulates Runx1 expression, which is necessary for normal cartilage formation.
颅指(趾)骨发育不良综合征(TRPS)是一种常染色体显性遗传骨骼疾病,由 Trps1 基因突变引起,该基因编码一种 GATA 型转录抑制因子。为了研究 Trps1 下游的基因,我们使用 ATDC5 细胞进行了 DNA 芯片分析。从 DNA 芯片中鉴定的一个靶基因是 Runx1,它对造血至关重要,并且与 Runx2 一样,在软骨生成中发挥重要作用。荧光素酶启动子测定和染色体免疫沉淀测定表明,Trps1 通过结合 P2 启动子的 GATA 结构域抑制了鼠骺板软骨中 Runx1 的表达;该启动子为 Runx1 基因的两个近端片段。原位杂交检测到 Trps1 缺失小鼠生长板软骨细胞中 P2 转录本的异常表达。总之,Trps1 结合到 Runx1 基因的 P2 启动子上并下调 Runx1 的表达,这对于正常软骨形成是必需的。