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热疗会阻碍细胞核基质中的DNA处理过程。

Hyperthermia blocks DNA processing at the nuclear matrix.

作者信息

Warters R L

机构信息

Department of Radiology, University of Utah Health Sciences Center, Salt Lake City 84132.

出版信息

Radiat Res. 1988 Aug;115(2):258-72.

PMID:3406367
Abstract

The capacity of control and heated HeLa cells to process newly polymerized DNA at the nuclear matrix was measured. DNA which had been pulse-labeled with [3H]thymidine was enriched by a factor of up to 6 at the cell's nuclear matrix. During continuous exposure to [3H]thymidine at 37 degrees C this enrichment for pulse-labeled DNA was reversed with a half-time of 7 min. We interpret this processing of newly replicated DNA to be a distribution of newly polymerized DNA throughout replicon-sized nuclear DNA domains. Both processing of newly polymerized DNA at the nuclear matrix and ligation of replicon clusters into the interphase cell chromosome were halted by incubation of cells at temperatures at or above 43 degrees C. When HeLa cells were pulse-labeled during a 30-min incubation at 45 degrees C and replaced at 37 degrees C, the enrichment for 3H-labeled DNA at the nuclear matrix was reversed with an initial half-time of 4 h. The results indicate that exposure of cells to hyperthermic temperatures blocks ongoing nascent DNA processing at the nuclear matrix and results in a retardation of DNA processing in preheated cells replaced at 37 degrees C.

摘要

测量了对照和经加热处理的HeLa细胞在核基质中处理新聚合DNA的能力。用[³H]胸苷脉冲标记的DNA在细胞核基质中富集了高达6倍。在37℃持续暴露于[³H]胸苷期间,这种脉冲标记DNA的富集以7分钟的半衰期逆转。我们将这种新复制DNA的处理解释为新聚合DNA在整个复制子大小的核DNA结构域中的分布。在43℃或更高温度下孵育细胞会阻止新聚合DNA在核基质中的处理以及复制子簇连接到间期细胞染色体中。当HeLa细胞在45℃下孵育30分钟期间进行脉冲标记并在37℃下更换时,核基质中³H标记DNA的富集以4小时的初始半衰期逆转。结果表明,细胞暴露于高温会阻断核基质中正在进行的新生DNA处理,并导致在37℃下更换的预热细胞中DNA处理延迟。

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