概括
编码血小板衍生生长因子 (PDGF) 链的人类SIS原瘤基因获得了转化活性. 在c-sis克隆8中添加一个上游的外因子,使sis/PDGF-2蛋白表达和细胞转化成为可能.
科学领域:
- 分子生物学分子生物学
- 瘤基因是一种瘤基因.
- 细胞转化 细胞转化
背景情况:
- 人类SIS原瘤基因编码了血小板衍生生长因子 (PDGF) 的多链.
- 发现含有v-sis相关序列的特定人类DNA克隆 (c-sis克隆8) 在NIH/3T3细胞中是转录不活跃的.
研究的目的:
- 研究人类系统原瘤基因的转化潜力.
- 确定SIS/PDGF-2表达和生物活性所需的监管元素.
主要方法:
- 在逆转录病毒LTR控制下,NIH/3T3细胞感染c-sis克隆8.
- 使用与SIS相关的转录探测器识别一个假定的上游外基因.
- 构建和转化一个虚构的LTR-exon-c-sis克隆8分子.
主要成果:
- 单独c-sis克隆8没有显示可检测的sis/PDGF-2蛋白表达或转化活性.
- 被识别的上游外基子,当插入时,赋予了高位的转化活性.
- 转化细胞表达人体SIS/PDGF-2转化产物,表明功能激活.
结论:
- 人体生长因子 (sis/PDGF-2) 的正常编码序列具有转化潜力.
- 特定的监管元素,如已识别的上游外基子,对于其表达和致癌活性至关重要.
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