纤毛原生动物的程序性染色体断裂:通往染色体末端的多种途径。

IF 8 1区 生物学 Q1 MICROBIOLOGY Microbiology and Molecular Biology Reviews Pub Date : 2023-12-20 Epub Date: 2023-11-27 DOI:10.1128/mmbr.00184-22
Mireille Bétermier, Lawrence A Klobutcher, Eduardo Orias
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引用次数: 0

摘要

纤毛虫原生动物在偶联过程中形成新的转录活性大核时,其体细胞基因组经历了大规模的发育重排。这个过程包括来自种系的染色体的断裂,加上通过重新添加端粒有效地愈合断裂的末端。在这里,我们回顾了在分子水平上已经得到充分研究的纤毛虫(Tetrahymena,草履虫,Euplotes, Stylonychia和Oxytricha)中已知的发育染色体片段。这些生物在片段系统的保真度和精确度上存在很大差异,也存在或不存在明确定义的序列元素来指导切除,这表明染色体片段系统已经进化了多次和/或在纤毛虫进化过程中发生了重大变化。我们提出了当前纤毛虫系统进化的两阶段模型,这两个阶段都涉及基因组中的重复或转座元件。染色体断裂的祖先形式被认为源自纤毛虫在发育过程中从大核基因组中去除转座子和其他重复元件的小RNA/染色质修饰过程。这一祖先系统的进化被认为加强了它在一些纤毛虫谱系中被后来的由移动遗传元素产生的破碎系统所取代。
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Programmed chromosome fragmentation in ciliated protozoa: multiple means to chromosome ends.

SUMMARYCiliated protozoa undergo large-scale developmental rearrangement of their somatic genomes when forming a new transcriptionally active macronucleus during conjugation. This process includes the fragmentation of chromosomes derived from the germline, coupled with the efficient healing of the broken ends by de novo telomere addition. Here, we review what is known of developmental chromosome fragmentation in ciliates that have been well-studied at the molecular level (Tetrahymena, Paramecium, Euplotes, Stylonychia, and Oxytricha). These organisms differ substantially in the fidelity and precision of their fragmentation systems, as well as in the presence or absence of well-defined sequence elements that direct excision, suggesting that chromosome fragmentation systems have evolved multiple times and/or have been significantly altered during ciliate evolution. We propose a two-stage model for the evolution of the current ciliate systems, with both stages involving repetitive or transposable elements in the genome. The ancestral form of chromosome fragmentation is proposed to have been derived from the ciliate small RNA/chromatin modification process that removes transposons and other repetitive elements from the macronuclear genome during development. The evolution of this ancestral system is suggested to have potentiated its replacement in some ciliate lineages by subsequent fragmentation systems derived from mobile genetic elements.

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来源期刊
CiteScore
18.80
自引率
0.80%
发文量
27
期刊介绍: Microbiology and Molecular Biology Reviews (MMBR), a journal that explores the significance and interrelationships of recent discoveries in various microbiology fields, publishes review articles that help both specialists and nonspecialists understand and apply the latest findings in their own research. MMBR covers a wide range of topics in microbiology, including microbial ecology, evolution, parasitology, biotechnology, and immunology. The journal caters to scientists with diverse interests in all areas of microbial science and encompasses viruses, bacteria, archaea, fungi, unicellular eukaryotes, and microbial parasites. MMBR primarily publishes authoritative and critical reviews that push the boundaries of knowledge, appealing to both specialists and generalists. The journal often includes descriptive figures and tables to enhance understanding. Indexed/Abstracted in various databases such as Agricola, BIOSIS Previews, CAB Abstracts, Cambridge Scientific Abstracts, Chemical Abstracts Service, Current Contents- Life Sciences, EMBASE, Food Science and Technology Abstracts, Illustrata, MEDLINE, Science Citation Index Expanded (Web of Science), Summon, and Scopus, among others.
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