Trendelenburg M F, Zatsepina O V, Waschek T, Schlegel W, Tröster H, Rudolph D, Schmahl G, Spring H
German Cancer Research Centre (DKFZ), Heidelberg, Germany.
Histochem Cell Biol. 1996 Aug;106(2):167-92. doi: 10.1007/BF02484399.
A survey of novel microscopic approaches for structural and functional analysis of subnucleolar compartments will be presented. Research on nucleolar structure and function concentrates predominantly on two distinct types of nucleoli: (1) nucleoli present during the interphase of the cell cycle in somatic tissue culture cells and (2) nucleoli present in meiotic cells, e.g. oocytes of amphibians. These nucleoli are found during meiotic prophase of oogenesis and are functional during several months of the diplotene stage of oogenesis. A further characteristic is the fact that these nucleoli are extrachromosomal, since they originate by selective ribosomal DNA (rDNA) amplification during the early pachytene stage of oogenesis. Miller-type chromatin spread preparations using transcriptionally active nucleoli, to a major part, contributed to our understanding of the structural organization of polymerase I directed pre-rRNA transcription. Although the structural organization of the template-associated pre-rRNA transcript is known in some detail from chromatin spreads, relatively little is known about structural aspects of pre-rRNA processing. In order to investigate this intriguing question in more detail, we have developed a computer-based densitometry analysis of both template-associated and template-dissociated pre-rRNA transcripts in order to follow the structural modification of pre-rRNA transcripts during processing. Another line of experiments is devoted to the in situ structure of actively transcribing genes in the nucleolus. In order to bridge the gap between light microscopy and electron microscopy we started video-enhanced light microscopical analysis of actively transcribing genes. Although the dimensions of individual spread genes are critical for detection by optical microscopy, we succeeded in obtaining the first series of images of transcribing genes in their "native' hydrated state. An additional promising type of microscopy is transmission X-ray microscopy. Recent progress in instrumentation as well as in sample preparation has allowed us to obtain the first images of density distribution within intact, fully hydrated nucleoli using amplitude-contrast and/or phase-contrast X-ray microscopy of non-contrasted, fully hydrated nucleoli at different states of transcriptional activity. Whereas the above mentioned investigations using video microscopy and X-ray microscopy are predominantly applicable to the analysis of amplified nucleoli in amphibian oocytes, which are characterized by an extremely high transcription rate of 80-90% of rDNA genes per individual nucleolus, structural analysis of the in situ arrangement of actively transcribing genes in somatic nucleoli as present in the interphase nucleus is far more difficult to perform, mainly due to the much lower number of simultaneously transcribed active genes per individual nucleolus. Visualization of actively transcribed gene clusters is approached by an integrated experimental assay using video microscopy, confocal laser scan microscopy, and antibodies against specific nucleolar proteins.
将介绍一项关于核仁亚区室结构和功能分析的新型微观方法的调查。对核仁结构和功能的研究主要集中在两种不同类型的核仁上:(1)体细胞组织培养细胞细胞周期间期存在的核仁,以及(2)减数分裂细胞中存在的核仁,例如两栖类动物的卵母细胞。这些核仁在卵子发生的减数分裂前期被发现,并在卵子发生双线期的几个月内发挥功能。另一个特点是这些核仁是染色体外的,因为它们在卵子发生的粗线期早期通过选择性核糖体DNA(rDNA)扩增产生。使用转录活性核仁的米勒型染色质铺展制备方法在很大程度上有助于我们理解聚合酶I指导的前体rRNA转录的结构组织。尽管从染色质铺展中已经较为详细地了解了与模板相关的前体rRNA转录本的结构组织,但对于前体rRNA加工的结构方面了解相对较少。为了更详细地研究这个有趣的问题,我们开发了一种基于计算机的密度测定分析方法,用于分析与模板相关和与模板解离的前体rRNA转录本,以便跟踪前体rRNA转录本在加工过程中的结构修饰。另一系列实验致力于核仁中活跃转录基因的原位结构研究。为了弥合光学显微镜和电子显微镜之间的差距,我们开始对活跃转录基因进行视频增强光学显微镜分析。尽管单个铺展基因的尺寸对于光学显微镜检测至关重要,但我们成功获得了处于“天然”水合状态的转录基因的首批图像系列。另一种有前景的显微镜类型是透射X射线显微镜。仪器设备以及样品制备方面的最新进展使我们能够使用不同转录活性状态下未染色、完全水合的核仁的振幅对比和/或相位对比X射线显微镜,获得完整、完全水合核仁内密度分布的首批图像。上述使用视频显微镜和X射线显微镜的研究主要适用于分析两栖类动物卵母细胞中扩增的核仁,其特征是每个核仁中rDNA基因的转录率极高,达到80 - 90%,而对间期核中存在的体细胞核仁中活跃转录基因原位排列的结构分析则要困难得多,主要原因是每个核仁中同时转录的活跃基因数量要少得多。通过使用视频显微镜、共聚焦激光扫描显微镜以及针对特定核仁蛋白的抗体的综合实验分析方法来实现对活跃转录基因簇的可视化。