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Lovastatin selectively inhibits ras activation of the 12-O-tetradecanoylphorbol-13-acetate response element in mammalian cells. 总被引:1,自引:0,他引:1 下载免费PDF全文
D Defeo-Jones E M McAvoy R E Jones G A Vuocolo K M Haskell R J Wegrzyn A Oliff 《Molecular and cellular biology》1991,11(4):2307-2310
To evaluate ras-mediated signal transduction, an alkaline phosphatase gene (SEAP) was placed under the control of the ras-inducible phorbol ester response element (TRE) in murine fibroblasts (TRE-SEAP cells). The Kirsten ras gene was placed under the control of the glucocorticoid-inducible mouse mammary tumor virus promoter and introduced into the TRE-SEAP cells. Dexamethasone increased ras expression in the TRE-SEAP cells carrying the Kirsten ras gene and stimulated SEAP activity 25-fold. Lavostatin blocked dexamethasone induction of SEAP activity (50% inhibitory concentration, 0.5 microM) but did not affect phorbol ester-induced SEAP activity in the same cells. Lovastatin also did not block forskolin induction of SEAP activity in cells expressing SEAP under the control of the cyclic AMP response element. 相似文献
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Gordon Haskell 《Plant and Soil》1954,5(2):170-181
Summary A review is given of diseases and pests attacking North American inbred, hybrid and open-pollinated strains of sweet corn in England. Genetical and environmental influences are considered as problems of adaptation. Cold tolerance, susceptibility to smut, and fungi attacking ripening grain are under genetical control, but modified by environmental conditions. Analysis of these factors helps to control these diseases. Strains differ in resistance to frit fly attacks, and this is modified by sowing time. Frit flies and wireworms, acting independently or together, may limit sweet corn growing in some areas, while aphids also attack some inbred lines. Various methods of insect control are suggested. Mice and birds eat seeds, and bird damage may also limit maize growing. An outline suggests genetical and non-genetical modes of future control for diseases and insect pests when adaptating sweet corn to new climatic and other factors. These include selection for and use of resistant strains, or control by sowing at specific times. 相似文献
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W Kiess J F Haskell L Lee L A Greenstein B E Miller A L Aarons M M Rechler S P Nissley 《The Journal of biological chemistry》1987,262(26):12745-12751
To better define the biologic function of the type II insulin-like growth factor (IGF) receptor, we raised a blocking antiserum in a rabbit by immunizing with highly purified rat type II IGF receptor. On immunoblots of crude type II receptor preparations, only bands corresponding to the type II IGF receptor were seen with IgG 3637, indicating that the antiserum was specific for the type II receptor. Competitive binding and chemical cross-linking experiments showed that IgG 3637 blocked binding of 125I-IGF-II to the rat type II IGF receptor, but did not block binding of 125I-IGF-I to the type I IGF receptor, nor did IgG 3637 block binding of 125I-insulin to the insulin receptor. In addition, IgG 3637 did not inhibit the binding of 125I-IGF-II to partially purified 150- and 40-kDa IGF carrier proteins from adult and fetal rat serum. L6 myoblasts have both type I and type II IGF receptors. IGF-I was more potent than IGF-II in stimulating N-methyl-alpha-[14C]aminoisobutyric acid uptake, 2-[3H]deoxyglucose uptake, and [3H]leucine incorporation into cellular proteins. IgG 3637 did not stimulate either 2-[3H]deoxyglucose uptake, N-methyl-alpha-[14C]aminoisobutyric acid uptake, or [3H]leucine incorporation into protein when tested alone. Furthermore, IgG 3637 at concentrations sufficient to block type II receptors under conditions of the uptake and incorporation experiments did not cause a shift to the right of the dose-response curve for stimulation of these biologic functions by IGF-II. We conclude that the type II IGF receptor does not mediate IGF stimulation of N-methyl-alpha-[14C]aminoisobutyric acid and 2-[3H]deoxyglucose uptake and protein synthesis in L6 myoblasts; presumably, the type I receptor mediates these biologic responses. The anti-type II receptor antibody inhibited IGF-II degradation in the media by greater than 90%, suggesting that the major degradative pathway for IGF-II in L6 myoblasts utilizes the type II IGF receptor. 相似文献