多腺苷酸化信号的进化动态及其在原生动物中的识别策略

IF 6.2 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Genome research Pub Date : 2024-09-26 DOI:10.1101/gr.279526.124
Marcin P Sajek, Danielle Y Bilodeau, Michael A Beer, Emma Horton, Yukiko Miyamoto, Katrina B Velle, Lars Eckmann, Lillian Fritz-Laylin, Olivia S Rissland, Neelanjan Mukherjee
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引用次数: 0

摘要

poly(A) 信号与辅助元件一起指导前 mRNA 的裂解,从而决定成熟转录本的 3' 端。在包括人类在内的许多物种中,poly(A)信号是一个 AAUAAA 六聚体,但我们最近发现,深枝真核生物蓝氏贾第鞭毛虫使用一种独特的六聚体(AGURAA),而且缺乏任何已知的辅助元件。这一发现促使我们探索真核生物王国中聚(A)信号和辅助元件的进化动态。我们使用直接 RNA 测序来确定 Metamonada 支系(也包括蓝氏贾第鞭毛虫)中四种原生动物和两种外群原生动物的 poly(A) 信号。这些实验表明,AAUAAA 六聚体在至少四个不同的真核生物支系中充当聚(A)信号,这表明它很可能是祖先的信号,而不常见的贾第鞭毛虫信号则是衍生信号。我们发现,辅助元件的使用和相对强度也具有惊人的可塑性;事实上,在 Metamonada 中,像蓝氏贾第鞭毛虫这样的物种使用了一种以前未被认识到的辅助元件,在这种辅助元件中,聚(A)信号本身侧翼的核苷酸指定了真正的裂解位点。因此,尽管前核糖核酸(pre-mRNA)的裂解是所有编码蛋白质基因表达的基础,但控制这一过程的基调在进化时间尺度上是动态的,这为未来的生物化学和结构研究以及针对真核病原体的新治疗角度提供了动力。
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Evolutionary dynamics of polyadenylation signals and their recognition strategies in protists
The poly(A) signal, together with auxiliary elements, directs cleavage of a pre-mRNA and thus determines the 3' end of the mature transcript. In many species, including humans, the poly(A) signal is an AAUAAA hexamer, but we recently found that the deeply branching eukaryote Giardia lamblia uses a distinct hexamer (AGURAA) and lacks any known auxiliary elements. Our discovery prompted us to explore the evolutionary dynamics of poly(A) signals and auxiliary elements in the eukaryotic kingdom. We used direct RNA sequencing to determine poly(A) signals for four protists within the Metamonada clade (which also contains Giardia lamblia) and two outgroup protists. These experiments revealed that the AAUAAA hexamer serves as the poly(A) signal in at least four different eukaryotic clades, indicating that it is likely the ancestral signal, whereas the unusual Giardia version is derived. We found that the use and relative strengths of auxiliary elements are also surprisingly plastic; in fact, within Metamonada, species like Giardia lamblia make use of a previously unrecognized auxiliary element where nucleotides flanking the poly(A) signal itself specify genuine cleavage sites. Thus, despite the fundamental nature of pre-mRNA cleavage for the expression of all protein-coding genes, the motifs controlling this process are dynamic on evolutionary timescales, providing motivation for future biochemical and structural studies as well as new therapeutic angles to target eukaryotic pathogens.
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来源期刊
Genome research
Genome research 生物-生化与分子生物学
CiteScore
12.40
自引率
1.40%
发文量
140
审稿时长
6 months
期刊介绍: Launched in 1995, Genome Research is an international, continuously published, peer-reviewed journal that focuses on research that provides novel insights into the genome biology of all organisms, including advances in genomic medicine. Among the topics considered by the journal are genome structure and function, comparative genomics, molecular evolution, genome-scale quantitative and population genetics, proteomics, epigenomics, and systems biology. The journal also features exciting gene discoveries and reports of cutting-edge computational biology and high-throughput methodologies. New data in these areas are published as research papers, or methods and resource reports that provide novel information on technologies or tools that will be of interest to a broad readership. Complete data sets are presented electronically on the journal''s web site where appropriate. The journal also provides Reviews, Perspectives, and Insight/Outlook articles, which present commentary on the latest advances published both here and elsewhere, placing such progress in its broader biological context.
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