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感染人腺病毒5型野生型和转化缺陷型宿主范围突变体的KB细胞中早期病毒蛋白的合成动力学

The kinetics of synthesis of early viral proteins in KB cells infected with wild-type and transformation-defective host-range mutants of human adenovirus type 5.

作者信息

Rowe D T, Branton P E, Graham F L

出版信息

J Gen Virol. 1984 Mar;65 ( Pt 3):585-97. doi: 10.1099/0022-1317-65-3-585.

Abstract

We have studied the kinetics of early adenovirus type 5 (Ad5) protein synthesis during lytic infection of KB cells by wild-type (wt) and transformation-defective host-range (hr) mutants. Proteins encoded within four early regions were studied: early region 1A (E1A: 1.5 to 4.5 map units, mu), E1B (4.5 to 11.2 mu), E2A (61.6 to 74.9 mu), and E4 (91.4 to 99.1 mu). Synthesis of E1A products, the first to appear during wt lytic infection, was detectable within 2 h after injection, reached a peak within the next hour, then declined to very low levels by 7 h post-infection. Synthesis of E2 and E4 proteins began at about 3 h post-infection, was maximal by 6 h and thereafter declined sharply. The E1B 19K and 58K proteins were first detected around 3 h post-infection and, after reaching maximal levels of expression by 8 h, declined to lower levels by 12 h post-infection. Infections with the E1A mutant hr3 were characterized by greatly depressed levels of early expression of E1B, E2 and E4 polypeptides but protein synthesis from these regions appeared to recover at late times. The pattern of expression exhibited by the E1B mutant hr6 revealed delayed and reduced levels of expression of E1B, E2 and E4 protein synthesis but increased levels of E1A protein synthesis. These results are consistent with the reported role of E1A gene products in the activation of early gene expression and, in addition, suggest that a function encoded in E1B may also influence the expression of Ad5 early genes at early and late times.

摘要

我们研究了野生型(wt)和转化缺陷型宿主范围(hr)突变体在KB细胞裂解感染期间5型腺病毒(Ad5)早期蛋白质合成的动力学。研究了四个早期区域编码的蛋白质:早期区域1A(E1A:1.5至4.5图单位,mu)、E1B(4.5至11.2 mu)、E2A(61.6至74.9 mu)和E4(91.4至99.1 mu)。E1A产物是wt裂解感染期间最早出现的,在注射后2小时内即可检测到,在接下来的1小时内达到峰值,然后在感染后7小时降至非常低的水平。E2和E4蛋白的合成在感染后约3小时开始,在6小时达到最大值,此后急剧下降。E1B 19K和58K蛋白在感染后约3小时首次检测到,在8小时达到最大表达水平后,在感染后12小时降至较低水平。用E1A突变体hr3感染的特征是E1B、E2和E4多肽的早期表达水平大大降低,但这些区域的蛋白质合成在后期似乎恢复。E1B突变体hr6表现出的表达模式显示E1B、E2和E4蛋白合成的表达延迟且水平降低,但E1A蛋白合成水平增加。这些结果与报道的E1A基因产物在早期基因表达激活中的作用一致,此外,还表明E1B中编码的一种功能也可能在早期和晚期影响Ad5早期基因的表达。

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