MALE GERM CELL-SPECIFIC ALTERATION IN TEMPERATURE SET-POINT OF THE CELLULAR STRESS-RESPONSE

被引:79
作者
SARGE, KD
机构
[1] Department of Biochemistry, Chandler Medical Center, University of Kentucky, Lexington
[2] Dept. of Biochemistry, University of Kentucky, Lexington, KY 40536-0084
关键词
D O I
10.1074/jbc.270.32.18745
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Heat shock factor (HSF), a transcriptional regulator with heat-activatable DNA binding ability, mediates the stress-induced expression of eukaryotic heat shock protein genes, Previous results from this laboratory demonstrated that a preparation of mixed male germ cell types from mouse testis exhibited a lower temperature threshold for activation of HSF1 DNA binding relative to other mouse cell types (Sarge, K. D., Pray, A. E., and Goodson, M. L. (1995) Nature 374, 126), The purpose of the present study was to determine whether the phenomenon of reduced HSF1 activation temperature is common to all testis cell types, both somatic and germ cell types, or whether it is a special property of male germ cells, The results show that a purified population of pachytene spermatocytes, one of the male germ cell types, exhibits a profile of reduced HSF1 activation temperature identical to that observed for the mixed germ cell preparation, with a threshold HSF1 activation temperature of 35 degrees C, Activation of HSF1 DNA binding in male germ cells by incubation at 38 degrees C is accompanied by the classic cellular stress response parameters of heat-induced HSF1 phosphorylation and increased expression of the hsp72 stress protein, In contrast, a preparation of somatic testis cell types exhibits HSF1 activation only at temperatures of 42 degrees C and above, a profile identical to that observed for mouse liver cells and mammalian cell lines, These results demonstrate that the phenomenon of reduced HSF1 activation temperature is a unique property of male germ cell types within the mammalian testis and demonstrate that HSF1 activated at this lower temperature threshold is fully capable of mediating a productive cellular stress response in these cell types.
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页码:18745 / 18748
页数:4
相关论文
共 37 条
[1]   ATTENUATION OF THE HEAT-SHOCK RESPONSE IN HELA-CELLS IS MEDIATED BY THE RELEASE OF BOUND HEAT-SHOCK TRANSCRIPTION FACTOR AND IS MODULATED BY CHANGES IN GROWTH AND IN HEAT-SHOCK TEMPERATURES [J].
ABRAVAYA, K ;
PHILLIPS, B ;
MORIMOTO, RI .
GENES & DEVELOPMENT, 1991, 5 (11) :2117-2127
[2]   A NOVEL HSP70-LIKE PROTEIN (P70) IS PRESENT IN MOUSE SPERMATOGENIC CELLS [J].
ALLEN, RL ;
OBRIEN, DA ;
EDDY, EM .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (02) :828-832
[3]   EXPRESSION OF HEAT-SHOCK PROTEINS BY ISOLATED MOUSE SPERMATOGENIC CELLS [J].
ALLEN, RL ;
OBRIEN, DA ;
JONES, CC ;
ROCKETT, DL ;
EDDY, EM .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (08) :3260-3266
[4]   ABNORMAL PROTEINS SERVE AS EUKARYOTIC STRESS SIGNALS AND TRIGGER THE ACTIVATION OF HEAT-SHOCK GENES [J].
ANANTHAN, J ;
GOLDBERG, AL ;
VOELLMY, R .
SCIENCE, 1986, 232 (4749) :522-524
[5]   ACTIVATION OF HUMAN HEAT-SHOCK GENES IS ACCOMPANIED BY OLIGOMERIZATION, MODIFICATION, AND RAPID TRANSLOCATION OF HEAT-SHOCK TRANSCRIPTION FACTOR HSF1 [J].
BALER, R ;
DAHL, G ;
VOELLMY, R .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (04) :2486-2496
[6]   INDUCTION TEMPERATURE OF HUMAN HEAT-SHOCK FACTOR IS REPROGRAMMED IN A DROSOPHILA CELL ENVIRONMENT [J].
CLOS, J ;
RABINDRAN, S ;
WISNIEWSKI, J ;
WU, C .
NATURE, 1993, 364 (6434) :252-255
[7]   HEAT-SHOCK PROTEINS - MOLECULAR CHAPERONES OF PROTEIN BIOGENESIS [J].
CRAIG, EA ;
GAMBILL, BD ;
NELSON, RJ .
MICROBIOLOGICAL REVIEWS, 1993, 57 (02) :402-414
[8]  
Eddy EM, 1993, MOL BIOL MALE REPROD, P181
[9]   POSTMEIOTIC GENE-EXPRESSION [J].
ERICKSON, RP .
TRENDS IN GENETICS, 1990, 6 (08) :264-269
[10]  
HARRISON RG, 1948, J PHYSIOL-LONDON, V107, pP48