小鼠随机序列和新生进化基因在人类细胞中的表达揭示了功能多样性和特异性。

IF 3.2 2区 生物学 Q2 EVOLUTIONARY BIOLOGY Genome Biology and Evolution Pub Date : 2024-12-04 DOI:10.1093/gbe/evae175
Silvia Aldrovandi, Johana Fajardo Castro, Kristian Ullrich, Amir Karger, Victor Luria, Diethard Tautz
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引用次数: 0

摘要

从非编码DNA中重新产生的蛋白质可以在提供可能的适应性优势的意义上消极或积极地影响细胞生理学。在这里,我们采用两种方法通过表达人类基因组中缺乏同源基因的随机序列和小鼠新生基因来研究人类细胞系中的这种效应。我们表明,这两种方法导致依赖于它们表达的序列的细胞克隆的不同生长效应。对于随机序列,53%的克隆频率下降,而在联合生长实验中,大约8%的克隆频率增加。在一个类似的关节生长实验中测试的14个小鼠新生基因中,10个减少,3个增加。当单独分析时,每个小鼠新生基因都会在人类细胞中触发独特的转录组反应,表明大多是特异性的而不是普遍的影响。对新生基因开放阅读框(orf)的结构分析揭示了一系列内在的紊乱分数和/或可折叠成α螺旋或β薄片,但这些与它们对细胞生长的影响无关。我们的研究结果表明,新生进化的orf可以很容易地整合到细胞调节途径中,因为大多数orf与这些途径的成分相互作用,因此如果一般条件允许,orf可以直接受到正选择的影响。
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Expression of Random Sequences and de novo Evolved Genes From the Mouse in Human Cells Reveals Functional Diversity and Specificity.

Proteins that emerge de novo from noncoding DNA could negatively or positively influence cellular physiology in the sense of providing a possible adaptive advantage. Here, we employ two approaches to study such effects in a human cell line by expressing random sequences and mouse de novo genes that lack homologs in the human genome. We show that both approaches lead to differential growth effects of the cell clones dependent on the sequences they express. For the random sequences, 53% of the clones decreased in frequency, and about 8% increased in frequency in a joint growth experiment. Of the 14 mouse de novo genes tested in a similar joint growth experiment, 10 decreased, and 3 increased in frequency. When individually analysed, each mouse de novo gene triggers a unique transcriptomic response in the human cells, indicating mostly specific rather than generalized effects. Structural analysis of the de novo gene open reading frames (ORFs) reveals a range of intrinsic disorder scores and/or foldability into alpha-helices or beta sheets, but these do not correlate with their effects on the growth of the cells. Our results indicate that de novo evolved ORFs could easily become integrated into cellular regulatory pathways, since most interact with components of these pathways and could therefore become directly subject to positive selection if the general conditions allow this.

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来源期刊
Genome Biology and Evolution
Genome Biology and Evolution EVOLUTIONARY BIOLOGY-GENETICS & HEREDITY
CiteScore
5.80
自引率
6.10%
发文量
169
审稿时长
1 months
期刊介绍: About the journal Genome Biology and Evolution (GBE) publishes leading original research at the interface between evolutionary biology and genomics. Papers considered for publication report novel evolutionary findings that concern natural genome diversity, population genomics, the structure, function, organisation and expression of genomes, comparative genomics, proteomics, and environmental genomic interactions. Major evolutionary insights from the fields of computational biology, structural biology, developmental biology, and cell biology are also considered, as are theoretical advances in the field of genome evolution. GBE’s scope embraces genome-wide evolutionary investigations at all taxonomic levels and for all forms of life — within populations or across domains. Its aims are to further the understanding of genomes in their evolutionary context and further the understanding of evolution from a genome-wide perspective.
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