FEBS Letters
Volume 581, Issue 19 , Pages 3702-3710, 31 July 2007

The heat shock protein 70 family: Highly homologous proteins with overlapping and distinct functions

Edited by Dr. Robert Barouki

Apoptosis Department and Centre for Genotoxic Stress Response, Institute of Cancer Biology, Danish Cancer Society, Strandboulevarden 49, DK-2100 Copenhagen, Denmark

Received 17 March 2007; received in revised form 14 May 2007; accepted 14 May 2007. published online 24 May 2007.

Abstract 

The human heat shock protein 70 (Hsp70) family contains at least eight homologous chaperone proteins. Endoplasmatic reticulum and mitochondria have their specific Hsp70 proteins, whereas the remaining six family members reside mainly in the cytosol and nucleus. The requirement for multiple highly homologous although different Hsp70 proteins is still far from clear, but their individual and tissue-specific expression suggests that they are assigned distinct biological tasks. This concept is supported by the fact that mice knockout for different Hsp70 genes display remarkably discrete phenotypes. Moreover, emerging data suggest that individual Hsp70 proteins can bring about non-overlapping and chaperone-independent functions essential for growth and survival of cancer cells. This review summarizes our present knowledge of the individual members of human Hsp70 family and elaborate on the functional differences between the cytosolic/nuclear representatives.

Abbreviations: CBF, CCAAT-box binding factor, ER, endoplasmatic reticulum, Hsc70, heat shock cognate 70, HSE, heat shock element, HSF, heat shock factor, Hsp70, heat shock protein 70, MHC, major histocompatibility complex, siRNA, small interfering RNA, TNF, tumor necrosis factor

Keywords: Cancer, Cell death, Evolution, Gene expression, Heat shock proteins, Thermotolerance

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PII: S0014-5793(07)00567-4

doi:10.1016/j.febslet.2007.05.039

FEBS Letters
Volume 581, Issue 19 , Pages 3702-3710, 31 July 2007