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蛋白激酶A对果蝇NF1突变表型的挽救作用

Rescue of a Drosophila NF1 mutant phenotype by protein kinase A.

作者信息

The I, Hannigan G E, Cowley G S, Reginald S, Zhong Y, Gusella J F, Hariharan I K, Bernards A

机构信息

Massachusetts General Hospital Cancer Center and Harvard Medical School Building 149, 13th Street, Charlestown, MA 02129, USA.

出版信息

Science. 1997 May 2;276(5313):791-4. doi: 10.1126/science.276.5313.791.

Abstract

The neurofibromatosis type 1 (NF1) tumor suppressor protein is thought to restrict cell proliferation by functioning as a Ras-specific guanosine triphosphatase-activating protein. However, Drosophila homozygous for null mutations of an NF1 homolog showed no obvious signs of perturbed Ras1-mediated signaling. Loss of NF1 resulted in a reduction in size of larvae, pupae, and adults. This size defect was not modified by manipulating Ras1 signaling but was restored by expression of activated adenosine 3', 5'-monophosphate-dependent protein kinase (PKA). Thus, NF1 and PKA appear to interact in a pathway that controls the overall growth of Drosophila.

摘要

1型神经纤维瘤病(NF1)肿瘤抑制蛋白被认为通过作为一种Ras特异性鸟苷三磷酸酶激活蛋白来限制细胞增殖。然而,果蝇中NF1同源基因纯合缺失突变体未表现出明显的Ras1介导信号传导紊乱迹象。NF1缺失导致幼虫、蛹和成虫体型减小。这种体型缺陷不会因操纵Ras1信号传导而改变,但可通过表达活化的3',5'-环磷酸腺苷依赖性蛋白激酶(PKA)得以恢复。因此,NF1和PKA似乎在控制果蝇整体生长的一条通路中相互作用。

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