TY - JOUR
T1 - Heat stress of cultured GC cells enhances triiodothyronine-induced growth hormone production by action within the 5′- flanking region of the rat growth hormone gene
AU - Mokshagundam, Sri Prakash
AU - Shapiro, Lawrence E.
AU - Surks, Martin I.
N1 - Funding Information:
Herbert H. Samuels for providing the Christine Frawley and Evette Gonzalez for This work was supported by NIH Grants and NIH Training Grant AM 07004 (to S.M.)
PY - 1992/10/30
Y1 - 1992/10/30
N2 - We studied the effect of incubation at 41 C on a clone of GC cells that had previously been stably transfected with a gene construct, pGHXGPT, containing -1800 to +8 of the rat growth hormone promoter fused to the structural gene for E. Coli xanthine guanine phosphor ibosyl-transferase. The effect of incubation of the clone containing pGHXGPT at 41 C was to enhance triiodothyronine induction of growth hormone secretion (2-fold, p<0.01) and of xanthine quanine phosphoribosyl-transferase activity (3-fold, p< 0.01). We conclude that the increase in triiodothyronine-induced growth hormone production during heat stress occurs by stimulation of the growth hormone promoter.
AB - We studied the effect of incubation at 41 C on a clone of GC cells that had previously been stably transfected with a gene construct, pGHXGPT, containing -1800 to +8 of the rat growth hormone promoter fused to the structural gene for E. Coli xanthine guanine phosphor ibosyl-transferase. The effect of incubation of the clone containing pGHXGPT at 41 C was to enhance triiodothyronine induction of growth hormone secretion (2-fold, p<0.01) and of xanthine quanine phosphoribosyl-transferase activity (3-fold, p< 0.01). We conclude that the increase in triiodothyronine-induced growth hormone production during heat stress occurs by stimulation of the growth hormone promoter.
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U2 - 10.1016/0006-291X(92)91104-X
DO - 10.1016/0006-291X(92)91104-X
M3 - Article
C2 - 1445309
AN - SCOPUS:0026496528
SN - 0006-291X
VL - 188
SP - 638
EP - 643
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -