基2的突变α子单元抑制循环AMP的积累
Y H Wong1, A Federman, A M Pace
1Department of Pharmacology, University of California, San Francisco 94143.
Nature
|May 2, 1991
概括
阿尔法i2基因的突变可以产生致癌瘤基因 (gip2). 这些突变导致蛋白质构成性地抑制循环AMP积累,影响细胞信号通路.
科学领域:
- 分子生物学分子生物学
- 细胞信号传输 细胞信号传输
- 瘤发生的发生因子.
背景情况:
- 腺环酶的荷尔蒙抑制涉及Gi蛋白 (Gi1-3),但介导子单元 (α或β gamma) 是未知的.
- 刺激性G蛋白 (Gs) 的α子单元的突变导致构成性激活,形成内分泌瘤中发现的gsp瘤基因.
研究的目的:
- 调查Gi2的α子单元中的突变是否会导致瘤原体的激活.
- 为了确定这些突变是否导致Gi2在腺酸环酶上抑制功能的构成性激活.
主要方法:
- 培养细胞被设计成表达野生类型或突变的αi2互补DNA.
- 周期性AMP积累在表达异源αi2变异的细胞中被测量.
主要成果:
- 在人类内分泌瘤中发现了Gi2的α子单元体内突变,类似于gsp突变.
- 这些突变将αi2基因转化为潜在的瘤基因 (gip2).
- 在实验中,突变的α i2子单元显示了循环AMP积累的构成性活性抑制.
结论:
- 阿尔法i2基因的突变可以产生具有主导作用的瘤基因 (gip2).
- 鉴定到的突变构成性地激活了α i2蛋白对循环AMP积累的抑制作用,类似于瘤性Gs.
- 这表明构成性活性Gi2在内分泌瘤发生中的作用.
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