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Recombineering Homologous Recombination Constructs in Drosophila
Published on: July 13, 2013
德洛索菲拉p53在收割者位置结合了一个损伤反应元素
M H Brodsky1, W Nordstrom, G Tsang
1Howard Hughes Medical Institute, Department of Molecular and Cell Biology, University of California, Berkeley, 94720, USA.
Cell
|April 25, 2000
概括
研究人员确定了Drosophila p53同类物,该同类物调节细胞对DNA损伤的反应. 这种基因直接准了亲死基因收割者,影响发育组织中的辐射诱导的亡.
科学领域:
- 分子生物学分子生物学
- 遗传学 遗传学 是一个
- 发展生物学 发展生物学
背景情况:
- 瘤抑制剂p53对于细胞对DNA损伤的反应至关重要,但其转录性点在很大程度上仍然未知.
- 了解p53的调节网络对于破译DNA损伤反应途径至关重要.
研究的目的:
- 为了识别和表征Drosophila p53同类.
- 调查Drosophila p53在转录调节和DNA损伤后的亡中的作用.
- 为了确定亲遗传基因收割者是否是Drosophila p53.3的直接转录标.
主要方法:
- 克隆和特征一个Drosophila p53同类.
- 用酵母和培养细胞中的p53结合位点进行转录激活的测试.
- 在体内对主导阴性p53形式的功能分析.
- 鉴定和分析收割者基因的cis-regulatory区域.
- 在体内研究辐射诱导的基因表达.
主要成果:
- 鉴定出一种功能性Drosophila p53同类物,能够从人类的p53结合部位激活转录.
- 主导阴性Drosophila p53抑制了交换活化和辐射诱导的亡.
- 预性基因收割器具有具有p53结合点的辐射诱导增强剂.
- 在酵母和体内,Drosophila p53从收割者增强剂直接激活了转录.
结论:
- 德洛索菲拉p53作为对DNA损伤的反应中的转录调节剂.
- 收割者基因是Drosophila p53.3的直接转录标.
- 这项研究阐明了Drosophila中DNA损伤反应途径的关键组成部分,该途径与哺乳动物保持一致.
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