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实验性基因诱导后海德果蝇唾液腺中的蛋白质合成。

Protein synthesis in salivary glands of Drosophila hydei after experimental gene induction.

作者信息

Koninkx J F

出版信息

Biochem J. 1976 Sep 15;158(3):623-8. doi: 10.1042/bj1580623.

Abstract

Several treatments, namely incubation at 37 degrees C, in the presence of arsenite, 2,4-dinitrophenol or vitamin B-6, or release from anaerobiosis induce the same set of puffs in the polythene chromosomes of salivary glands of Drosophila hydei. Analysis of changes in protein-synthetic patterns (as determined by radioautography of sodium dodecyl sulphate-gel electrophoretograms of extracts from [35S]methionine-labelled salivary glands) showed that concomitant with puff induction by these various treatments the same six strongly labelled polypeptide bands appeared. The amount of radioactive label in these peptides accounted for 25% of the total incorporation of [35S]methionine, except during incubation at 37 degrees C when it accounted for about 50%. The rate of synthesis of these peptides was maximal 1 h after the start of the puff-inducing treatment. The rate of decay of the rate of synthesis showed first-order kinetics both after removal of the puff-inducing stimulus or in the presence of actinomycin, with a half-life of approx. 4h.

摘要

几种处理方法,即在37摄氏度下培养、在亚砷酸盐、2,4 -二硝基苯酚或维生素B - 6存在的情况下培养,或从厌氧状态释放,会在海德氏果蝇唾液腺的多线染色体中诱导出相同的一组胀泡。对蛋白质合成模式变化的分析(通过对[35S]甲硫氨酸标记的唾液腺提取物的十二烷基硫酸钠 - 凝胶电泳图谱进行放射自显影来确定)表明,伴随着这些不同处理诱导胀泡,出现了相同的六条强标记多肽带。这些肽中的放射性标记量占[35S]甲硫氨酸总掺入量的25%,但在37摄氏度培养时约占50%。这些肽的合成速率在胀泡诱导处理开始后1小时达到最大值。在去除胀泡诱导刺激后或在放线菌素存在的情况下,合成速率的衰减速率均呈现一级动力学,半衰期约为4小时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7221/1164017/567a81bdbfac/biochemj00526-0126-a.jpg

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