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体内给予(+)-麦角酸二乙酰胺后大脑多核糖体解聚后mRNA的命运

Fate of mRNA following disaggregation of brain polysomes after administration of (+)-lysergic acid diethylamide in vivo.

作者信息

Mahony J B, Brown I R

出版信息

Biochim Biophys Acta. 1979 Nov 22;565(1):161-72. doi: 10.1016/0005-2787(79)90092-3.

Abstract

Intravenous injection of (+)-lysergic acid diethylamide into young rabbits induced a transient brain-specific disaggregation of polysomes to monosomes. Investigation of the fate of mRNA revealed that brain poly(A+)mRNA was conserved. In particular, mRNA coding for brain-specific S100 protein was not degraded, nor was it released into free ribonucleoprotein particles. Following the (+)-lysergic acid diethylamide-induced disaggregation of polysomes, mRNA shifted from polysomes and accumulated on monosomes. Formation of a blocked monosome complex, which contained intact mRNA and 40-S plus 60-S ribosomal subunits but lacked nascent peptide chains, suggested that (+)-lysergic acid diethylamide inhibited brain protein synthesis at a specific stage of late initiation or early elongation.

摘要

向幼兔静脉注射(+)-麦角酸二乙酰胺会导致多核糖体短暂发生脑特异性解聚为单核糖体。对mRNA命运的研究表明,脑聚腺苷酸(poly(A+))mRNA得以保留。特别是,编码脑特异性S100蛋白的mRNA未被降解,也未释放到游离核糖核蛋白颗粒中。在(+)-麦角酸二乙酰胺诱导多核糖体解聚后,mRNA从多核糖体上转移并积累在单核糖体上。形成的封闭单核糖体复合物包含完整的mRNA以及40-S和60-S核糖体亚基,但缺乏新生肽链,这表明(+)-麦角酸二乙酰胺在起始后期或延伸早期的特定阶段抑制脑蛋白质合成。

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