Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague 128 00, Czech Republic.
Cells. 2021 Jan 20;10(2):196. doi: 10.3390/cells10020196.
In human cells, ribosomal DNA (rDNA) is arranged in ten clusters of multiple tandem repeats. Each repeat is usually described as consisting of two parts: the 13 kb long ribosomal part, containing three genes coding for 18S, 5.8S and 28S RNAs of the ribosomal particles, and the 30 kb long intergenic spacer (IGS). However, this standard scheme is, amazingly, often altered as a result of the peculiar instability of the locus, so that the sequence of each repeat and the number of the repeats in each cluster are highly variable. In the present review, we discuss the causes and types of human rDNA instability, the methods of its detection, its distribution within the locus, the ways in which it is prevented or reversed, and its biological significance. The data of the literature suggest that the variability of the rDNA is not only a potential cause of pathology, but also an important, though still poorly understood, aspect of the normal cell physiology.
在人类细胞中,核糖体 DNA(rDNA)排列在十个串联重复的簇中。每个重复通常被描述为由两部分组成:长 13kb 的核糖体部分,包含编码核糖体颗粒 18S、5.8S 和 28S RNA 的三个基因,以及长 30kb 的基因间 spacer(IGS)。然而,令人惊讶的是,由于该基因座的特殊不稳定性,这种标准方案经常发生改变,因此每个重复的序列和每个簇中的重复数量高度可变。在本综述中,我们讨论了人类 rDNA 不稳定性的原因和类型、其检测方法、其在基因座内的分布、防止或逆转它的方式以及它的生物学意义。文献数据表明,rDNA 的可变性不仅是病理学的潜在原因,也是正常细胞生理学的一个重要但仍未被充分理解的方面。