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大鼠1型神经纤维瘤病基因的差异剪接——与人同源的剪接变体在大鼠细胞中表达。

Differential splicing of the neurofibromatosis type-1 gene in the rat - splice variants homologous with the human are expressed in rat-cells.

作者信息

Kyritsis A, Lee P, Mochizuki H, Nishi T, Levin V, Saya H

机构信息

UNIV TEXAS,MD ANDERSON CANC CTR,DEPT NEUROONCOL,BOX 100,1515 HOLCOMBE BLVD,HOUSTON,TX 77030.

出版信息

Int J Oncol. 1992 Jul;1(2):149-52.

Abstract

The GTPase activating protein-related domain (GRD) of the human neurofibromatosis type 1 gene (NF1) was shown to have two types of splice variants. Through polymerase chain reaction (PCR), we isolated and sequenced three types of splice variants in the rat NF1-GRD. Type I and II transcripts were highly homologous with the human transcripts. The type III NF1-GRD transcript, unidentified in the human, had an additional 41-bp insert immediately downstream from the 63-bp insert of the type II transcript. The type III transcript encoded for a protein that prematurely terminated its predicted amino acid sequence because of a stop codon, resulting in possible modification of the GAP activity. All three transcripts were found in the rat's liver, cerebral hemispheres, spinal cord, colon, and spleen, whereas the other organs examined had only type I and II transcripts. This differential splicing mechanism may regulate the activity or compartmentalization of the NF1 protein, resulting in modulation of the Ras-related signal transduction pathway.

摘要

人类1型神经纤维瘤病基因(NF1)的GTP酶激活蛋白相关结构域(GRD)显示有两种类型的剪接变体。通过聚合酶链反应(PCR),我们在大鼠NF1 - GRD中分离并测序了三种类型的剪接变体。I型和II型转录本与人类转录本高度同源。III型NF1 - GRD转录本在人类中未被鉴定出来,它在II型转录本63个碱基对插入片段的紧下游有一个额外的41个碱基对的插入片段。III型转录本编码的蛋白质由于一个终止密码子使其预测的氨基酸序列过早终止,可能导致GAP活性的改变。在大鼠的肝脏、大脑半球、脊髓、结肠和脾脏中均发现了所有三种转录本,而所检查的其他器官仅含有I型和II型转录本。这种差异剪接机制可能调节NF1蛋白的活性或分隔,从而导致对Ras相关信号转导通路的调节。

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