Sparkowski J, Anders J, Schlegel R
Department of Pathology, Georgetown University, Washington, DC 20007, USA.
EMBO J. 1995 Jul 3;14(13):3055-63. doi: 10.1002/j.1460-2075.1995.tb07308.x.
The E5 oncoprotein encoded by bovine papillomavirus type 1 is a homodimeric, hydrophobic polypeptide which is localized predominantly in Golgi membranes and which transforms several cell types apparently by inducing tyrosine phosphorylation of the platelet-derived growth factor receptor (PDGF-R). While the precise mechanism of receptor activation is unknown, E5 associates with several cellular proteins, including PDGF-R and the 16K V-ATPase protein, and induces the preferential phosphorylation of immature, Endo H-sensitive forms of the receptor. To evaluate whether E5 accumulation in the Golgi was requisite for receptor phosphorylation and cell transformation, we sequestered the E5 protein in the endoplasmic reticulum (ER)/cis Golgi by appending the ER retention KDEL sequence to its C-terminus. In transient assays and in cell lines, E5/KDEL protein and E5/KDEL* protein (a defective variant of KDEL), were stable and formed homodimers normally. E5/KDEL*, similar to wt E5, localized to the Golgi and was transformation-proficient. In contrast, E5/KDEL failed to concentrate in the Golgi and was transformation-incompetent. Despite these critical defects, however, E5/KDEL formed stable complexes with immature PDGF-R and 16K and, even more unexpectedly, induced the phosphorylation of both mature and immature PDGF-R on tyrosine residues to the same level as wt E5. These data demonstrate that E5 can bind and induce PDGF-R phosphorylation in the ER/cis Golgi, but that successful mitogenic signalling (and consequent cell transformation) requires the translocation of E5/receptor complexes to distal Golgi compartments.
1型牛乳头瘤病毒编码的E5癌蛋白是一种同二聚体疏水多肽,主要定位于高尔基体膜,它通过诱导血小板衍生生长因子受体(PDGF-R)的酪氨酸磷酸化,明显地转化多种细胞类型。虽然受体激活的确切机制尚不清楚,但E5与几种细胞蛋白相关联,包括PDGF-R和16K V-ATP酶蛋白,并诱导受体未成熟的、内切糖苷酶H敏感形式的优先磷酸化。为了评估E5在高尔基体中的积累对于受体磷酸化和细胞转化是否必要,我们通过在其C末端附加内质网(ER)保留KDEL序列,将E5蛋白隔离在内质网/顺式高尔基体中。在瞬时分析和细胞系中,E5/KDEL蛋白和E5/KDEL蛋白(KDEL的缺陷变体)是稳定的,并且正常形成同二聚体。E5/KDEL与野生型E5相似,定位于高尔基体且具有转化能力。相比之下,E5/KDEL未能在高尔基体中聚集,并且没有转化能力。然而,尽管存在这些关键缺陷,E5/KDEL与未成熟的PDGF-R和16K形成稳定复合物,甚至更出乎意料的是,它诱导成熟和未成熟PDGF-R的酪氨酸残基磷酸化,达到与野生型E5相同的水平。这些数据表明,E5可以在内质网/顺式高尔基体中结合并诱导PDGF-R磷酸化,但成功的促有丝分裂信号传导(以及随之而来的细胞转化)需要E5/受体复合物转运至高尔基体远端区室。