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1型神经纤维瘤病基因编码一种与GAP相关的蛋白质。

The neurofibromatosis type 1 gene encodes a protein related to GAP.

作者信息

Xu G F, O'Connell P, Viskochil D, Cawthon R, Robertson M, Culver M, Dunn D, Stevens J, Gesteland R, White R

机构信息

Department of Human Genetics, University of Utah School of Medicine, Salt Lake City 84132.

出版信息

Cell. 1990 Aug 10;62(3):599-608. doi: 10.1016/0092-8674(90)90024-9.

Abstract

cDNA walking and sequencing have extended the open reading frame for the neurofibromatosis type 1 gene (NF1). The new sequence now predicts 2485 amino acids of the NF1 peptide. A 360 residue region of the new peptide shows significant similarity to the known catalytic domains of both human and bovine GAP (GTPase activating protein). A much broader region, centered around this same 360 amino acid sequence, is strikingly similar to the yeast IRA1 product, which has a similar amino acid sequence and functional homology to mammalian GAP. This evidence suggests that NF1 encodes a cytoplasmic GAP-like protein that may be involved in the control of cell growth by interacting with proteins such as the RAS gene product. Mapping of the cDNA clones has confirmed that NF1 spans a t(1;17) translocation mutation and that three active genes lie within an intron of NF1, but in opposite orientation.

摘要

cDNA步移和测序扩展了1型神经纤维瘤病基因(NF1)的开放阅读框。新序列目前预测NF1肽有2485个氨基酸。新肽的一个360个残基区域与人及牛的GAP(GTP酶激活蛋白)的已知催化结构域有显著相似性。围绕这一相同的360个氨基酸序列的更广泛区域与酵母IRA1产物惊人地相似,IRA1产物与哺乳动物GAP有相似的氨基酸序列和功能同源性。这一证据表明,NF1编码一种细胞质GAP样蛋白,它可能通过与RAS基因产物等蛋白质相互作用参与细胞生长的控制。cDNA克隆的定位证实,NF1跨越一个t(1;17)易位突变,并且三个活性基因位于NF1的一个内含子内,但方向相反。

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