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从青蛙和蝾螈的活卵母细胞中分离巨大灯刷染色体。

Isolation of Giant Lampbrush Chromosomes from Living Oocytes of Frogs and Salamanders.

作者信息

Gall Joseph G, Nizami Zehra F

机构信息

Department of Embryology, Carnegie Institution for Science;

Department of Embryology, Carnegie Institution for Science.

出版信息

J Vis Exp. 2016 Dec 5(118):54103. doi: 10.3791/54103.

Abstract

We describe methods for studying the giant transcriptionally active lampbrush chromosomes (LBCs) found in the oocyte, or unlaid egg, of frogs and salamanders. Individual LBCs can be up to 1 mm in length and they reside in a gigantic nucleus, itself up to 0.5 mm in diameter. The large size of the chromosomes permits unparalleled observations of active genes by light optical microscopy, but at the same time special techniques are required for isolating the nucleus, removing the nuclear envelope, and spreading the chromosomes on a microscope slide. The oocyte nucleus, also called the germinal vesicle (GV), is isolated in a medium that allows partial gelling of the nuclear actin and preserves the delicate structure of the LBCs. This step is carried out manually under a dissecting microscope using jeweler's forceps. Next, the nuclear envelope is removed, again manually with jeweler's forceps. The nuclear contents are quickly transferred to a medium that disperses the actin gel and allows the undamaged LBCs to settle onto a microscope slide. At this point the LBCs and other nuclear organelles can be viewed by phase contrast or differential interference contrast microscopy, although finer details are obscured by Brownian motion. For high resolution microscopical observation or molecular analysis, the whole preparation is centrifuged to attach the delicate LBCs firmly to the slide. A brief fixation in paraformaldehyde is then followed by immunofluorescent staining or in situ hybridization. LBCs are in a transcriptionally active state and their enormous size permits molecular analysis at the individual gene level using confocal or super-resolution microscopy.

摘要

我们描述了研究在青蛙和蝾螈的卵母细胞或未产卵中发现的巨大转录活性灯刷染色体(LBCs)的方法。单个LBCs的长度可达1毫米,它们存在于一个巨大的细胞核中,该细胞核本身直径可达0.5毫米。染色体的巨大尺寸使得通过光学显微镜对活跃基因进行无与伦比的观察成为可能,但与此同时,需要特殊技术来分离细胞核、去除核膜并将染色体铺展在显微镜载玻片上。卵母细胞核,也称为生发泡(GV),在一种能使核肌动蛋白部分凝胶化并保留LBCs精细结构的培养基中分离出来。这一步骤在解剖显微镜下使用珠宝镊子手动进行。接下来,同样用珠宝镊子手动去除核膜。将核内容物迅速转移到一种能分散肌动蛋白凝胶并使未受损的LBCs沉淀到显微镜载玻片上的培养基中。此时,可以通过相差显微镜或微分干涉相差显微镜观察LBCs和其他核细胞器,尽管更精细的细节会被布朗运动掩盖。为了进行高分辨率显微镜观察或分子分析,将整个制备物离心,使精细的LBCs牢固地附着在载玻片上。然后用多聚甲醛进行短暂固定,接着进行免疫荧光染色或原位杂交。LBCs处于转录活跃状态,其巨大尺寸使得使用共聚焦或超分辨率显微镜在单个基因水平上进行分子分析成为可能。

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