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培养的两栖类细胞中新基因表达的冷休克和热休克诱导

Cold- and heat-shock induction of new gene expression in cultured amphibian cells.

作者信息

Ketola-Pirie C A, Atkinson B G

出版信息

Can J Biochem Cell Biol. 1983 Jun;61(6):462-71. doi: 10.1139/o83-062.

DOI:10.1139/o83-062
PMID:6603891
Abstract

Exposing primary epidermal cell cultures from the American bullfrog Rana catesbeiana to elevated (greater than or equal to 32 degrees C; heat shock) or depressed (less than or equal to 5 degrees C; cold shock) temperatures for a short time results in the new and (or) enhanced synthesis of a 65 000 dalton (isoelectric point (pI) 6.7-6.9) polypeptide. With increasing temperature, a marked decrease in the synthesis of polypeptides observed at the control temperature (22 degrees C) and the new and (or) enhanced synthesis of another polypeptide with a relative mass of 25 000 and a pI of 6.7-6.9 is noted. Following a 1-h incubation at 34 degrees C, at least 4 h of recovery (at 22 degrees C) is required for primary epidermal cultures to resume their preinduction pattern of protein synthesis. Similar studies using an established adult kidney epithelial cell line from the African claw-toed frog Xenopus laevis demonstrate that cells from this organism respond to heat shock but do not respond to cold shock. Xenopus cells respond to heat shock by the new and (or) enhanced synthesis of at least five polypeptides. In vitro translation of the mRNAs from heat-shocked Xenopus cells suggests that the heat-shock mRNAs from these cells are preferentially transcribed and translated during thermal stress.

摘要

将美国牛蛙(牛蛙)的原代表皮细胞培养物短时间暴露于升高的温度(大于或等于32摄氏度;热休克)或降低的温度(小于或等于5摄氏度;冷休克)下,会导致新合成和(或)增强合成一种65000道尔顿(等电点(pI)6.7 - 6.9)的多肽。随着温度升高,在对照温度(22摄氏度)下观察到的多肽合成显著减少,同时注意到新合成和(或)增强合成了另一种相对分子质量为25000且pI为6.7 - 6.9的多肽。在34摄氏度孵育1小时后,原代表皮培养物需要至少4小时的恢复时间(在22摄氏度)才能恢复其诱导前的蛋白质合成模式。使用来自非洲爪蟾(非洲爪蟾)的已建立的成年肾上皮细胞系进行的类似研究表明,该生物体的细胞对热休克有反应,但对冷休克无反应。非洲爪蟾细胞通过新合成和(或)增强合成至少五种多肽来对热休克做出反应。对热休克后的非洲爪蟾细胞的mRNA进行体外翻译表明,这些细胞的热休克mRNA在热应激期间优先转录和翻译。