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小鼠随机序列和从头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。

Expression of Random Sequences and de novo Evolved Genes From the Mouse in Human Cells Reveals Functional Diversity and Specificity.

作者信息

Aldrovandi Silvia, Fajardo Castro Johana, Ullrich Kristian, Karger Amir, Luria Victor, Tautz Diethard

机构信息

Max-Planck Institute for Evolutionary Biology, Dept. Evol. Genetics, Plön 24306, Germany.

RG Development & Disease, Max Planck Institute for Molecular Genetics, Berlin 14195, Germany.

出版信息

Genome Biol Evol. 2024 Dec 4;16(12). doi: 10.1093/gbe/evae175.

Abstract

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.

摘要

从非编码DNA中全新出现的蛋白质可能会对细胞生理产生负面或正面影响,从提供可能的适应性优势的意义上来说。在这里,我们采用两种方法在人类细胞系中研究此类效应,即表达随机序列和在人类基因组中缺乏同源物的小鼠全新基因。我们表明,这两种方法都会导致细胞克隆产生不同的生长效应,这取决于它们所表达的序列。对于随机序列,在联合生长实验中,53%的克隆频率下降,约8%的克隆频率增加。在类似的联合生长实验中测试的14个小鼠全新基因中,10个频率下降,3个频率增加。单独分析时,每个小鼠全新基因都会在人类细胞中引发独特的转录组反应,这表明大多是特异性而非普遍性的效应。对全新基因开放阅读框(ORF)的结构分析揭示了一系列内在无序分数和/或折叠成α螺旋或β折叠的能力,但这些与它们对细胞生长的影响无关。我们的结果表明,全新进化的ORF很容易融入细胞调节途径,因为大多数与这些途径的成分相互作用,因此如果一般条件允许,可能会直接受到正选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf3c/11635099/8ff924061abc/evae175f1.jpg

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