首页> 美国卫生研究院文献>Journal of Virology >Similar regulation of the synthesis of adenovirus fiber and of simian virus 40-specific proteins encoded by the helper-defective Ad2+SV40 hybrid viruses Ad2+ND5 and Ad2+ND4del.
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Similar regulation of the synthesis of adenovirus fiber and of simian virus 40-specific proteins encoded by the helper-defective Ad2+SV40 hybrid viruses Ad2+ND5 and Ad2+ND4del.

机译:由辅助缺陷型Ad2 + SV40杂种病毒Ad2 + ND5和Ad2 + ND4del编码的腺病毒纤维和猿猴病毒40特异性蛋白的合成的类似调控。

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摘要

Human adenoviruses fail to multiply effectively in monkey cells. The block to the replication of these viruses can be overcome by coinfection with simian virus 40 (SV40) or when part of the SV40 genome is integrated into and expressed as part of the adenovirus type 2 (Ad2) genome, as occurs in several Ad2+SV40 hybrid viruses, such as Ad2+ND1, Ad2+ND2, and Ad2+ND4. The SV40 helper-defective Ad2+SV40 hybrid viruses Ad2+ND5 and Ad2+ND4del were analyzed to determine why they are unable to grow efficiently in monkey cells even though they contain the appropriate SV40 genetic information. Characterization of the Ad2+ND5-SV40-specific 42,000-molecular-weight (42K) protein revealed that this protein is closely related, but not identical, to the SV40-specific 42K protein of the SV40 helper-competent Ad2+ND2 hybrid virus. Although the minor differences between these proteins may be sufficient to account for the poor growth of Ad2+ND5 in monkey cells, the most striking difference between helper-competent Ad2+ND2 and helper-defective Ad2+ND5 is in the production of the SV40-specific protein after infection of monkey cells. Whereas synthesis of the SV40-specific proteins of Ad2+ND2 is very similar in human and in monkey cells, production of the 42K protein of Ad2+ND5 is dramatically reduced in monkey cells compared with human cells. Similarly, the synthesis of the SV40-specific proteins of Ad2+ND4del is markedly reduced in monkey cells. Thus, it is likely that both Ad2+ND5 and Ad2+ND4del are helper defective because of a block in the production of their SV40-specific proteins rather than because their SV40-specific proteins are nonfunctional. This block, like the block to adenovirus fiber synthesis, is overcome by coinfection with SV40, with helper-competent hybrid viruses, or with host range mutants of adenoviruses. This suggests that the synthesis of fiber and the synthesis of SV40-specific proteins are similarly regulated in Ad2+SV40 hybrid viruses.
机译:人腺病毒无法在猴细胞中有效繁殖。这些病毒复制的障碍可以通过与猿猴病毒40(SV40)共感染或当一部分SV40基因组整合到腺病毒2型(Ad2)基因组中并作为其一部分表达时来克服,就像在多个Ad2 +中发生的一样SV40杂种病毒,例如Ad2 + ND1,Ad2 + ND2和Ad2 + ND4。分析了SV40辅助缺陷型Ad2 + SV40杂种病毒Ad2 + ND5和Ad2 + ND4del,以确定它们为何即使在猴子细胞中含有适当的SV40遗传信息也无法高效生长。 Ad2 + ND5-SV40特异性42,000分子量(42K)蛋白的表征表明,该蛋白与SV40辅助胜任的Ad2 + ND2杂种病毒的SV40特异性42K蛋白密切相关,但不完全相同。尽管这些蛋白质之间的微小差异可能足以说明猴细胞中Ad2 + ND5的不良生长,但具有辅助功能的Ad2 + ND2和具有辅助功能的Ad2 + ND5之间最显着的差异在于SV40-猴细胞感染后的特定蛋白。在人和猴细胞中,Ad2 + ND2的SV40特异性蛋白的合成非常相似,而在猴细胞中,与人细胞相比,Ad2 + ND5的42K蛋白的产生显着减少。同样,在猴细胞中,Ad2 + ND4del的SV40特异性蛋白的合成也明显减少。因此,Ad2 + ND5和Ad2 + ND4del都可能是辅助缺陷的,因为它们的SV40特异性蛋白的生产受阻,而不是因为它们的SV40特异性蛋白无功能。通过与SV40,具有辅助功能的杂合病毒或与腺病毒的宿主范围突变体共同感染,可以克服与腺病毒纤维合成类似的障碍。这表明在Ad2 + SV40杂种病毒中,纤维的合成和SV40特异性蛋白的合成受到类似的调节。

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