Suppr超能文献

黑腹果蝇早期胚胎发育过程中RNA合成的超微结构模式。

Ultrastructural patterns of RNA synthesis during early embryogenesis of Drosophila melanogaster.

作者信息

McKnight S L, Miller O L

出版信息

Cell. 1976 Jun;8(2):305-19. doi: 10.1016/0092-8674(76)90014-3.

Abstract

Chromatin was obtained from Drosophila melanogaster during early embryogenesis and examined by transmission electron microscopy. Nuclear contents spread at progressive stages of syncytial development show a low level of only non-nuclear template activity, and very few RNP fibril gradients extending over 2mum in length are observed. At the cellular blastoderm stage, newly activated nucleolar genes appear during the early portion of the first true cell cycle. Variation in the lengths of incomplete rRNP gradients indicates that the activation of each rRNA gene is independently controlled. All rRNA loci, whether having complete or incomplete gradients, exhibit high densities of nascent transcripts per unit length, suggesting that the rate of chromatin transcription, rather than the RNA polymarase I pool size, limits rRNA synthesis on individual genes. No more than half the rRNA genes are derepressed at this stage indicating that total rRNA synthesis is regulated by the number of genes activated. Non-nucleolar RNP fibril gradients covering up to 8 mum of genome are also first observed at the cellular blastoderm stage. Most of these gradients are differentiated from the short gradient first seen during syncytial growth by a lower density of transcribing RNA polymerases.

摘要

在早期胚胎发育过程中从黑腹果蝇获取染色质,并通过透射电子显微镜进行检查。在合胞体发育的不同阶段展开的核内容物显示仅具有低水平的非核模板活性,并且观察到长度超过2μm的RNP纤维梯度非常少。在细胞胚盘阶段,新激活的核仁基因出现在第一个真正细胞周期的早期。不完全rRNP梯度长度的变化表明每个rRNA基因的激活是独立控制的。所有rRNA基因座,无论具有完整还是不完整的梯度,每单位长度都表现出高密度的新生转录本,这表明染色质转录速率而非RNA聚合酶I库大小限制了单个基因上的rRNA合成。在这个阶段,不超过一半的rRNA基因被去抑制,这表明总rRNA合成受激活基因数量的调节。在细胞胚盘阶段也首次观察到覆盖长达8μm基因组的非核仁RNP纤维梯度。这些梯度中的大多数与合胞体生长期间首次出现的短梯度的区别在于转录RNA聚合酶的密度较低。

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