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Identification of new actin-associated polypeptides that are modified by viral transformation and changes in cell shape

机译:鉴定新的肌动蛋白相关多肽这些多肽可通过病毒转化和细胞形状变化进行修饰

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摘要

By using a monoclonal antibody we have identified a new polypeptide doublet (C4h and C4l) of Mr approximately 21 kD and pI 8 and 7, respectively, that is associated with and (at the immunofluorescence level) uniformly distributed on actin filament bundles in rat, mouse, and other vertebrate species. C4 is absent in neurones, erythrocytes, and skeletal muscle but the epitope is evolutionarily conserved as it is present in invertebrates such as molluscs and crustaceans. C4h is not found in cells such as lymphocytes and oncogenically transformed mesenchymal cells where actin stress fiber bundles are reduced in number or absent. C4l, on the other hand, is always present. C4h expression can also be blocked by switching normal nontransformed mesenchymal cells from adherent to suspension culture. Reexpression of C4h occurs 24 h after these cells are returned to normal adherent culture conditions, but can be blocked by either actinomycin D or cycloheximide, suggesting that the expression of this epitope is regulated at the transcriptional level.
机译:通过使用单克隆抗体,我们已经确定了一个新的多肽双峰(C4h和C41),分别约为21 kD和pI 8和7,分别与大鼠肌动蛋白丝束均匀分布(在免疫荧光水平),老鼠和其他脊椎动物。 C4在神经元,红细胞和骨骼肌中不存在,但由于它存在于无脊椎动物(例如软体动物和甲壳类动物)中,因此表位在进化上是保守的。在诸如肌动蛋白应激纤维束数量减少或缺失的淋巴细胞和致癌转化的间充质细胞等细胞中未发现C4h。另一方面,C41总是存在。通过将正常的未转化的间充质细胞从粘附培养转变为悬浮培养,也可以阻断C4h表达。这些细胞恢复到正常的贴壁培养条件后24小时,C4h的重新表达发生,但是可以被放线菌素D或环己酰亚胺阻断,这表明该表位的表达在转录水平上受到调节。

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