Premium
Ultraviolet light attenuates heat‐inducible gene expression
Author(s) -
Qiu Lin,
Welk Joseph F.,
Jurivich Donald A.
Publication year - 1997
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/(sici)1097-4652(199709)172:3<314::aid-jcp5>3.0.co;2-r
Subject(s) - gene expression , gene , ultraviolet light , biology , microbiology and biotechnology , chemistry , genetics , photochemistry
Ultraviolet light (UV) induces a stress response mediated through transcription factors such as NF‐kB and AP‐1, yet little is known about its effect on other transactivators of stress gene expression such as heat shock factor (HSF1). Analysis of UV‐treated HeLa cells unexpectedly revealed uncoupling of the heat shock response. UV weakly induced HSF1 into its DNA bound state and markedly attenuated heat‐inducible gene expression. HSF1 was further analyzed as a potential target for the uncharacteristic uncoupling of the thermal stress response by another type of stress. Heat‐inducible multimerization and nuclear translocation of HSF1 were found to be intact in UV‐treated cells; however, the monomeric rather than the multimeric form of HSF1 become hyperphosphorylated by UV. This effect could be partially abolished by the antioxidant N‐acetyl cysteine with partial reconstitution of hs gene expression. The reported role of a MAP kinase blockade of HSF1 transactivating properties could not be confirmed by an inhibitor of the MAP kinase pathway. Fibroblasts defective in SAP kinase activity also did not exhibit resistance to UV‐inducible phosphorylation of HSF1. Two‐dimensional phosphopeptide mapping of HSF1 revealed a single tryptic peptide to be affected by UV, but no new pattern of phosphorylation was evident relative to tryptic phosphopeptide profile observed in control cells. These data suggest that UV uncoupling of the hs response possibly involves steps in addition to those associated with phosphorylation the monomeric form of HSF1. J. Cell. Physiol. 172:314–322, 1997. © 1997 Wiley‐Liss, Inc.