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CHO细胞热敏感突变体及其野生型对应物在热休克后特定和一般蛋白质合成的变化。

Alterations in specific and general protein synthesis after heat shock in heat-sensitive mutants of CHO cells and their wild-type counterparts.

作者信息

Harvey W F, Bedford J S, Li G C

机构信息

Department of Radiology and Radiation Biology, Colorado State University, Fort Collins 80523.

出版信息

Radiat Res. 1990 Oct;124(1 Suppl):S88-97.

PMID:2236516
Abstract

The rates of general and specific protein synthesis were studied in two heat-sensitive strains of CHO cells (Harvey and Bedford, Radiat. Res. 113, 526-542, 1988), both of which show a reduced ability to develop thermotolerance following an initial 45 degrees C heat shock. After various labeling periods with [35S]methionine, wild-type and mutant labeled proteins were separated by one- and two-dimensional polyacrylamide gel electrophoresis. Autoradiograms showed differences in levels of synthesis of several proteins after a 45 degrees C heat shock. In particular, these were in the hsp-70 group referred to as hsp-70a, b, and c, having molecular weights of 76, 73, and 72 kDa and isoelectric focusing pH values of 5.7, 5.5, and 5.7, respectively. Of particular note were changes in the hsp-70c region of the autoradiograms. We found that there was perhaps a low level of synthesis of hsp-70c in unheated wild-type cells but none was detectable in the mutant lines. After an isosurvival (approximately 10%) pulse of 45 degrees C heat there was a gradual increase in the synthesis of hsp-70c for wild-type but a smaller increase for the heat-sensitive strain 36 (HS-36) cells. In contrast, for HS-23 cells there was a very large initial increase by 5 to 7 h after the heat pulse and then a rapid decrease to undetectable levels by 11 to 13 h. The inhibition and recovery of general protein synthesis for both mutant and wild-type cells was also measured following various heat treatments at 45 degrees C. We observed that inhibition and resumption to a "normal" rate of protein synthesis for HS-23 cells paralleled the same response observed for the wild-type 10B2 cells. In sharp contrast, the time for recovery from the inhibition of protein synthesis for HS-36 cells was severely reduced for all heating times tested. Our results show that the period of delay before resumption of protein synthesis after heating does not always correlate with heat sensitivity or the degree of thermotolerance development. Several explanations for these observations are possible. One is that while synthesis of certain heat-shock proteins may indeed be responsible for the development of thermotolerance, the timing of the synthesis of these proteins in relation to the period of inhibition of general protein synthesis is crucial to such development.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在两种对热敏感的中国仓鼠卵巢(CHO)细胞系(Harvey和Bedford,《辐射研究》113, 526 - 542, 1988)中研究了总蛋白合成率和特定蛋白合成率,这两种细胞系在最初45℃热休克后形成耐热性的能力均降低。在用[35S]甲硫氨酸进行不同标记期后,通过一维和二维聚丙烯酰胺凝胶电泳分离野生型和突变型标记蛋白。放射自显影片显示在45℃热休克后几种蛋白的合成水平存在差异。特别是在被称为hsp - 70a、b和c的hsp - 70组中,它们的分子量分别为76、73和72 kDa,等电聚焦pH值分别为5.7、5.5和5.7。放射自显影片的hsp - 70c区域的变化尤其值得注意。我们发现未加热的野生型细胞中可能存在低水平的hsp - 70c合成,但在突变细胞系中未检测到。在45℃热的等存活(约10%)脉冲后,野生型细胞中hsp - 70c的合成逐渐增加,而对热敏感的36号菌株(HS - 36)细胞的增加较小。相比之下,对于HS - 23细胞,在热脉冲后5至7小时有非常大的初始增加,然后在11至13小时迅速降至不可检测水平。在45℃进行各种热处理后,还测量了突变型和野生型细胞总蛋白合成的抑制和恢复情况。我们观察到,HS - 23细胞蛋白合成抑制和恢复到“正常”速率的情况与野生型10B2细胞观察到的相同反应相似。与之形成鲜明对比的是,对于所有测试的加热时间,HS - 36细胞从蛋白合成抑制中恢复的时间都严重缩短。我们的结果表明,加热后恢复蛋白合成之前的延迟时间并不总是与热敏感性或耐热性发展程度相关。对于这些观察结果有几种可能的解释。一种解释是,虽然某些热休克蛋白的合成可能确实与耐热性的发展有关,但这些蛋白的合成时间与总蛋白合成抑制期的关系对于这种发展至关重要。(摘要截短至400字)

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