The cell cycle and tuberous sclerosis.

Progress in cell cycle research Pub Date : 2003-01-01
Markus Hengstschläger, Margit Rosner
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Abstract

Tuberous sclerosis (TSC) is an autosomal dominant tumor suppressor gene syndrome occurring in about 1 in 6000 live births. Two genes have been shown to be responsible for this disease: TSC1 on chromosome 9q34, encoding hamartin, and TSC2 on chromosome 16p13.3, encoding tuberin. Although several different functions of these proteins have been described, the molecular mechanism for the development of TSC remains elusive. Mammalian and Drosophila TSC genes have been shown to be involved in cell cycle regulation. The Drosophila TSC genes have further been demonstrated to affect cell size control and to be related to the insulin signaling pathway. Very recent data provide evidence that mammalian TSC genes are also involved in cell size regulation.

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细胞周期与结节性硬化症。
结节性硬化症(TSC)是一种常染色体显性肿瘤抑制基因综合征,约6000例活产儿中有1例发生。有两个基因被证明是导致这种疾病的原因:染色体9q34上的TSC1编码错构体,染色体16p13.3上的TSC2编码结节蛋白。虽然这些蛋白的几种不同功能已经被描述,但TSC发展的分子机制仍然是难以捉摸的。哺乳动物和果蝇的TSC基因已被证明参与细胞周期调节。果蝇的TSC基因已被进一步证明影响细胞大小的控制,并与胰岛素信号通路有关。最近的数据表明,哺乳动物的TSC基因也参与细胞大小调节。
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