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禽成红细胞增多症病毒转化基因产物v-erb-B蛋白的亚细胞定位。

Subcellular localization of the v-erb-B protein, the product of a transforming gene of avian erythroblastosis virus.

作者信息

Privalsky M L, Bishop J M

出版信息

Virology. 1984 Jun;135(2):356-68. doi: 10.1016/0042-6822(84)90192-2.

Abstract

Avian erythroblastosis virus (AEV) is an oncogenic retrovirus capable of transforming both fibroblasts and immature erythroid cells. The v-erb-B locus within the AEV genome encodes a glycosylated protein, expression of which is required for oncogenic transformation of either cell type. Subcellular localization of the v-erb-B glycoprotein in AEV-transformed cells is reported here. Results indicate that the v-erb-B protein is synthesized on dense membrane fractions and appears to possess the properties of an integral membrane protein. The bulk of the v-erb-B protein remains with dense membranes after synthesis, although a small quantity may slowly become associated with the plasma membrane. The biogenesis and subcellular location of the v-erb-B protein are thus quite different from those of the transforming proteins that display protein kinase activity. These differences are especially provocative because the amino acid sequences of the v-erb-B protein and the protein kinases are closely related to one another.

摘要

禽成红细胞增多症病毒(AEV)是一种致癌逆转录病毒,能够转化成纤维细胞和未成熟的红细胞。AEV基因组中的v-erb-B基因座编码一种糖基化蛋白,两种细胞类型的致癌转化都需要该蛋白的表达。本文报道了v-erb-B糖蛋白在AEV转化细胞中的亚细胞定位。结果表明,v-erb-B蛋白在致密膜组分上合成,似乎具有整合膜蛋白的特性。虽然少量v-erb-B蛋白可能会缓慢地与质膜结合,但大部分v-erb-B蛋白在合成后仍保留在致密膜上。因此,v-erb-B蛋白的生物合成和亚细胞定位与具有蛋白激酶活性的转化蛋白截然不同。这些差异尤其引人注目,因为v-erb-B蛋白和蛋白激酶的氨基酸序列彼此密切相关。

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