首页> 外文期刊>The Journal of Reproduction and Development >Transcription of follicle-stimulating hormone subunit genes is modulated by porcine LIM homeobox transcription factors, LHX2 and LHX3
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Transcription of follicle-stimulating hormone subunit genes is modulated by porcine LIM homeobox transcription factors, LHX2 and LHX3

机译:猪LIM同源异型盒转录因子LHX2和LHX3调节促卵泡激素亚基基因的转录

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The LIM-homeobox transcription factors LHX2 and LHX3s (LHX3a and LHX3b) are thought to be involved in regulating the pituitary glycoprotein hormone subunit genes Cga and Fsh beta. These two factors show considerable differences in their amino acid sequences for DNA binding and protein-protein interactions and in their vital function in pituitary development. Hence, we compared the DNA binding properties and transcriptional activities of Cga and Fsh beta between LHX2 and LHX3s. A gel mobility shift assay for approximately 1.1 kb upstream of Cga and 2.0 kb upstream of Fsh beta varied in binding profiles between LHX2 and LHX3s. DNase I footprinting revealed DNA binding sites in 8 regions of the Cga promoter for LHX2 and LHX3s with small differences in the binding range and strength. In the Fsh beta promoter, 14 binding sites were identified for LHX2 and LHX3, respectively. There were alternative binding sites to either gene in addition to similar differences observed in the Cga promoter. The transcriptional activities of LHX2 and LHX3s according to a reporter assay showed cell-type dependent activity with repression in the pituitary gonadotrope lineage L beta T2 cells and stimulation in Chinese hamster ovary lineage CHO cells. Reactivity of LHX2 and LHX3s was observed in all regions, and differences were observed in the 5'-upstream region of Fsh beta. However, immunohistochemistry showed that LHX2 resides in a small number of gonadotropes in contrast to LHX3. Thus, LHX3 mainly controls Cga and Fsh beta expression.
机译:LIM同源盒转录因子LHX2和LHX3s(LHX3a和LHX3b)被认为参与调节垂体糖蛋白激素亚基基因Cga和Fsh beta。这两个因素在其用于DNA结合和蛋白质-蛋白质相互作用的氨基酸序列以及它们在垂体发育中的重要功能方面显示出相当大的差异。因此,我们比较了LHX2和LHX3之间Cga和Fsh beta的DNA结合特性和转录活性。 LHX2和LHX3之间的结合曲线在Cga上游约1.1 kb和Fsh beta上游约2.0 kb的凝胶迁移率迁移分析中有所不同。 DNase I足迹显示LHX2和LHX3的Cga启动子的8个区域中的DNA结合位点,结合范围和强度的差异很小。在Fsh beta启动子中,分别为LHX2和LHX3鉴定了14个结合位点。除了在Cga启动子中观察到的相似差异外,还有两个基因的结合位点。 LHX2和LHX3s的转录活性根据报告基因测定显示出细胞类型依赖性活性,其在垂体促性腺激素谱系LβT2细胞中受到抑制,并在中国仓鼠卵巢谱系CHO细胞中受到刺激。在所有区域均观察到LHX2和LHX3的反应性,并且在Fsh beta的5'上游区域观察到差异。但是,免疫组织化学显示,与LHX3相比,LHX2存在于少量的促性腺激素中。因此,LHX3主要控制Cga和Fsh beta表达。

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