Engberg J
Eur J Cell Biol. 1985 Jan;36(1):133-51.
This report reviews the structural and functional characteristics of the ribosomal RNA genes (rDNA) of the ciliate protozoan, Tetrahymena. The study of rDNA was initiated some 10 years ago in order to establish a model system for rRNA gene expression in lower eukaryotes. The system proved very useful for studying several aspects of rRNA gene expression so that a considerable amount of information on rDNA structure and function has accumulated during the past years as a result of studies done in several laboratories. The initial finding that starved Tetrahymena cells, upon refeeding, preferentially replicated their rDNA for up to 90 min before bulk macronuclear DNA synthesis resumed, greatly facilitated the first studies. This observation permitted the rDNA to be labeled selectively with isotopes and in this way it was possible to isolate rDNA in pure form, to study replicative intermediates of the rDNA and to study rDNA containing chromatin in intact nuclei without resorting to chromatin fractionation. As a result of these studies it was found that the macronuclear rDNA of all Tetrahymena species consisted of a homogeneous population of extrachromosomal, linear molecules with a size of about 20 kilobase-pairs (kb) containing two identical transcription units for pre-rRNA arranged in a reverse repeat orientation (palindromic symmetry). The origins of replication were localized to the central non-transcribed spacer region and it was shown that this region has a chromatin structure which is different from that of the transcribed region. The primary DNA sequence is now known in many parts of the rDNA molecule, including the central part (containing the replication origins), the telomeric parts and the regions containing the sites of transcription initiation and termination. Transcription studies demonstrated the presence of an intervening sequence (intron) in the 26S rRNA coding region in some strains of Tetrahymena. Interestingly, the intron is transcribed and later removed from the primary transcript as a result of a rather unusual reaction which can take place in vitro in the absence of added protein factors. The finding of interbreeding strains of the intron+ and intron- rDNA genotype provided physical markers on the genes and have made possible a description of the inheritance and allelic assortment of the Tetrahymena rDNA. These studies proved that the free, palindromic rDNA molecules of the macronucleus arise from a chromosomally integrated, micronuclear rDNA copy as a result of a conjugational dependent amplification event, and that the intron is inherited as a neutral character during sexual and vegetative reproduction.(ABSTRACT TRUNCATED AT 400 WORDS)
本报告综述了纤毛原生动物四膜虫核糖体RNA基因(rDNA)的结构和功能特征。大约10年前开始对rDNA进行研究,目的是建立一个用于研究低等真核生物rRNA基因表达的模型系统。该系统在研究rRNA基因表达的多个方面被证明非常有用,因此,由于几个实验室的研究,在过去几年中积累了大量关于rDNA结构和功能的信息。最初的发现是,饥饿的四膜虫细胞在重新喂食后,在大量大核DNA合成恢复之前,优先复制其rDNA长达90分钟,这极大地促进了最初的研究。这一观察结果使rDNA能够被同位素选择性标记,通过这种方式,可以以纯形式分离rDNA,研究rDNA的复制中间体,并研究完整细胞核中含rDNA的染色质,而无需进行染色质分级分离。这些研究的结果发现,所有四膜虫物种的大核rDNA由一组均一的染色体外线性分子组成,大小约为20千碱基对(kb),包含两个相同的前体rRNA转录单元,以反向重复方向排列(回文对称)。复制起点定位于中央非转录间隔区,并且表明该区域具有与转录区不同的染色质结构。现在已知rDNA分子许多部分的初级DNA序列,包括中央部分(包含复制起点)、端粒部分以及包含转录起始和终止位点的区域。转录研究表明,在某些四膜虫菌株的26S rRNA编码区存在一个间隔序列(内含子)。有趣的是,该内含子被转录,随后由于一种相当不寻常的反应而从初级转录本中去除,这种反应在没有添加蛋白质因子的情况下可以在体外发生。内含子+和内含子 - rDNA基因型杂交菌株的发现为基因提供了物理标记,并使得对四膜虫rDNA的遗传和等位基因分类的描述成为可能。这些研究证明,大核中游离的、回文的rDNA分子是由于接合依赖性扩增事件从染色体整合的微核rDNA拷贝产生的,并且内含子在有性和无性繁殖过程中作为中性特征遗传。(摘要截于400字)