两个基因定义的转基因作用位置协调调节重叠的肝脏特异性基因组
S Ruppert1, M Boshart, F X Bosch
1Institute of Cell and Tumor Biology, German Cancer Research Center, Heidelberg.
Cell
|June 1, 1990
概括
在小鼠中失去alf转基因作用因子会破坏新生儿肝功能,导致致死性. 葡萄糖皮质类药物和cAMP可以逆转这种效应,揭示alf和Tse-1的协调基因调节.
科学领域:
- 分子生物学分子生物学
- 发展生物学 发展生物学
- 遗传学 是一个遗传学.
背景情况:
- 在阿尔比诺位点附近有缺失的小鼠表现出致命的新生儿表型.
- 这种表型与传递作用因子,alf.的丧失有关.
- 新生儿肝功能在alf缺乏的小鼠中受损.
研究的目的:
- 为了识别由alf转基因作用因子调节的基因.
- 为了研究葡萄糖皮质类药物和cAMP在alf介导基因表达中的作用.
- 探索alf和组织特定灭火器位点Tse-1之间的相互作用.
主要方法:
- 差异性cDNA选以隔离alf响应基因.
- 对激素刺激的反应中基因表达模式的分析.
- 研究Tse-1对alf调节基因的影响.
主要成果:
- 鉴定了转录受alf.影响的基因.
- 发现alf响应基因是由葡萄糖皮质类药物和cAMP诱导的.
- 发现Tse-1负控制了一组alf响应基因的子集.
- 证明葡萄糖皮质类药物和cAMP可以克服Tse-1-介导的抑制.
结论:
- 两个转基因作用因子,alf和Tse-1,协调重叠的肝脏特异性基因组的调节.
- 致命的表型和灭绝的基因表达可能是由于激素信号转导通路的破坏造成的.
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