Suppr超能文献

家蚕滞育前胚胎中基因表达的调控:蛋白质合成模式

Regulation of gene expression in prediapausing embryos of the silkworm, Bombyx mori: pattern of protein synthesis.

作者信息

Dorel C, Coulon M

机构信息

Laboratoire de Biologie Cellulaire, UA CNRS No. 92, Université Claude Bernard Lyon, Villeurbanne, France.

出版信息

Cell Differ. 1988 Mar;23(1-2):87-92. doi: 10.1016/0045-6039(88)90040-1.

Abstract

Specific qualitative and quantitative changes in protein synthesis occur from the fertilization to the onset of diapause in the silkworm. We have used two-dimensional gel electrophoresis to analyse the patterns of proteins synthesized in prediapausing eggs of Bombyx. This analysis has been carried out with in vivo labelled polypeptides and with proteins synthesized in vitro by RNA isolated at different stages. The oocyte contains an abundant supply of diverse mRNA which are translatable in vitro. A set of proteins with molecular weight range of 68,000 to 74,000 and isoelectric points of 5.85-5.95 (hereafter referred to as No. 30) is specific of the germ-anlage stage. Transcripts encoding the No. 30 proteins are not detectable in oocytes, and inhibition of transcription by actinomycin D indicates that No. 30 mRNA are synthesized de novo. Treating eggs at the germ-anlage stage with 4 N HCl at 46 degrees C prevents diapause and is accompanied by overproduction of No. 30 protein. The induction of No. 30 synthesis is also the main event of the heat shock response. The implications of these findings in relation to early embryonic development and prevention of diapause are discussed.

摘要

从家蚕受精到滞育开始,蛋白质合成会发生特定的定性和定量变化。我们利用二维凝胶电泳分析了家蚕滞育前卵中合成的蛋白质模式。该分析使用了体内标记的多肽以及不同阶段分离的RNA体外合成的蛋白质。卵母细胞含有丰富多样的可在体外翻译的mRNA。一组分子量范围为68,000至74,000且等电点为5.85 - 5.95的蛋白质(以下简称30号蛋白)是胚盘期特有的。在卵母细胞中检测不到编码30号蛋白的转录本,放线菌素D对转录的抑制表明30号mRNA是重新合成的。在46摄氏度下用4N盐酸处理胚盘期的卵可防止滞育,并伴随着30号蛋白的过量产生。30号蛋白合成的诱导也是热休克反应的主要事件。讨论了这些发现与早期胚胎发育和滞育预防的关系。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验