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首页> 外文期刊>Journal of cellular biochemistry. >The rate of folate receptor alpha (FR alpha) synthesis in folate depleted CHL cells is regulated by a translational mechanism sensitive to media folate levels, while stable overexpression of its mRNA is mediated by gene amplification and an increase
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The rate of folate receptor alpha (FR alpha) synthesis in folate depleted CHL cells is regulated by a translational mechanism sensitive to media folate levels, while stable overexpression of its mRNA is mediated by gene amplification and an increase

机译:叶酸耗尽的CHL细胞中叶酸受体α(FR alpha)的合成速率受对培养基叶酸水平敏感的翻译机制调控,而其mRNA的稳定过表达则是由基因扩增和增加介导的。

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摘要

DC-3F/FA3 cells (FA3) were obtained by selection of Chinese hamster lung fibroblasts for growth in folic acid free media, supplemented with 15 pM [6S]-5-formyltetrahydrofolic acid. These cells, as a result of low level gene amplification and RNA stabilization, were found to overexpress folate receptor alpha (FR alpha) mRNA by more than five hundred fold. The expression level of the receptor, a 43 kDa GPI-linked plasma membrane glycoprotein, was found to be inversely related to changes in media folate concentrations while its steady state mRNA level remained unaffected. In low folate, the rate of receptor synthesis was found to increase by more than three fold, while its half-life stabilized as compared to that observed in high folate media. Although DC-3F cells were found to contain low amounts of FR alpha mRNA, receptor expression was undetectable, and changing media folate concentrations had no effect on the expression of either. Hence, while selection for growth in low folate leads to stable overexpression of FR alpha mRNA, receptor expression is regulated at the level of protein synthesis by a mechanism sensitive to media folate levels. Copyright 2001 Wiley-Liss, Inc.
机译:DC-3F / FA3细胞(FA3)是通过选择中国仓鼠肺成纤维细胞在无叶酸培养基中生长,并补充15 pM [6S] -5-甲酰基四氢叶酸而获得的。由于低水平基因扩增和RNA稳定,这些细胞被发现过量表达叶酸受体α(FR alpha)mRNA 500倍以上。发现该受体的表达水平是一种43 kDa GPI连接的质膜糖蛋白,与培养基叶酸浓度的变化呈反相关,而其稳态mRNA水平却不受影响。在低叶酸中,与高叶酸培养基中观察到的相比,发现受体合成速率增加了三倍以上,同时其半衰期得以稳定。尽管发现DC-3F细胞含有少量的FRαmRNA,但是受体表达却无法检测到,改变培养基叶酸的浓度对两者的表达均无影响。因此,尽管在低叶酸中生长的选择导致稳定的FRαmRNA表达,但受体表达是通过对培养基叶酸水平敏感的机制在蛋白质合成水平上调节的。版权所有2001 Wiley-Liss,Inc.

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