Genomic Instability and Enhanced Radiosensitivity in Hsp70.1-and Hsp70.3 -Deficient Mice

Clayton R. Hunt, David J. Dix, Girdhar G. Sharma, Raj K. Pandita, Arun Gupta, Margo Funk, Tej K. Pandita

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205 Scopus citations


Heat shock proteins (HSPs) are highly conserved among all organisms from prokaryotes to eukaryotes. In mice, the HSP genes Hsp70.1 and Hsp70.3 are induced by both endogenous and exogenous stressors, such as heat and toxicants. In order to determine whether such proteins specifically influence genomic instability, mice deficient for Hsp70.1 and Hsp70.3 (Hsp70.1/3-/- mice) were generated by gene targeting. Mouse embryonic fibroblasts (MEFs) prepared from Hsp70.1/3-/- mice did not synthesize Hsp70.1 or Hsp70. 3 after heat-induced stress. While the Hsp70.1/3-/- mutant mice were fertile, their cells displayed genomic instability that was enhanced by heat treatment. Cells from Hsp70.1/3-/- mice also display a higher frequency of chromosome end-to-end associations than do control Hsp70.1/3 +/+ cells. To determine whether observed genomic instability was related to defective chromosome repair, Hsp70.1/3-/- and Hsp70.1/3+/+ fibroblasts were treated with ionizing radiation (IR) alone or heat and IR. Exposure to IR led to more residual chromosome aberrations, radioresistant DNA synthesis (a hallmark of genomic instability), increased cell killing, and enhanced IR-induced oncogenic transformation in Hsp70.1/3-/- cells. Heat treatment prior to IR exposure enhanced cell killing, S-phase-specific chromosome damage, and the frequency of transformants in Hsp70.1/3-/- cells in comparison to Hsp70.1/3 +/+ cells. Both in vivo and in vitro studies demonstrate for the first time that Hsp70.1 and Hsp70.3 have an essential role in maintaining genomic stability under stress conditions.

Original languageEnglish
Pages (from-to)899-911
Number of pages13
JournalMolecular and cellular biology
Issue number2
StatePublished - Jan 2004


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