数字DNA系统支持单向遗传优于“拉马克式”遗传。

IF 3.6 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
PLoS Computational Biology Pub Date : 2025-10-07 eCollection Date: 2025-10-01 DOI:10.1371/journal.pcbi.1012677
Aswathi Shiju, Samantha D M Arras, Allen G Rodrigo, Anthony M Poole
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引用次数: 0

摘要

在生物学中,DNA序列的变化可以影响蛋白质序列,但蛋白质序列(表型)的变化不会回流到DNA(基因型)中。具有双向信息流的系统(即翻译和“反向翻译”)仍然是生命或人工生物系统独立起源的理论可能性,但最近在DNA中数字数据存储的发展正是这样做的:对数字文件的更改可以写回DNA,这意味着对“表型”的更改可以写回“基因型”。为了探索这样一个系统的进化特性,我们创建了一个人工系统,其中合成DNA作为基因型,音乐作为表型。音频可以从DNA序列中输出,然后以“密码子”的形式记录并写入DNA,从而实现双向信息流(DNA→音乐和音乐→DNA)。我们的研究结果表明,双向系统中的突变率远远高于单向信息流,并且在反向翻译下,没有跨代保存密码子选择的机制。这消除了自发同义突变的影响,这是冗余遗传密码的一个关键好处。因此,非同义突变是唯一的跨代传递的dna水平变化,并且,由于非同义突变可以在“基因型”和“表型”水平上出现,这些突变的发生频率比单向系统高两倍。我们的系统有一些实际的见解。首先,对于DNA读/写系统,避免设计带有“从头开始的反向翻译”的系统可能是明智的,因为突变的机会更高;跟踪前一代的基因型信息来指导这一过程可以减少错误。其次,我们的系统有助于阐明“拉马克式”生物系统的运作方式。我们的结论是,如果“拉马克”遗传系统是早期遗传系统的一个特征,那么它很可能是短命的,因为高频率的突变可能会导致系统灭绝。基于单向信息流的系统因此显得更优越,因为产生突变错误的机会更少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A digital DNA system favours the superiority of unidirectional inheritance over 'Lamarckian' inheritance.

In biology, changes to a DNA sequence can impact protein sequence but changes to protein sequences (phenotype) do not flow back into DNA (genotype). A system with bidirectional information flow (i.e., both translation and 'reverse translation') remains a theoretical possibility for an independent origin of life or an artificial biosystem, but the recent development of digital data storage in DNA does just this: changes made to a digital file can be written back into DNA, meaning changes to 'phenotype' can be written back to 'genotype'. To explore the evolutionary properties of such a system, we created an artificial system where synthetic DNA serves as genotype and music as phenotype. Audio can be output from a DNA sequence, then recorded and written to DNA as 'codons', enabling bidirectional information flow (DNA→music and music→DNA). Our results show that the mutation rate in a bidirectional system is much higher than for unidirectional information flow, and that, under reverse translation there is no mechanism for preservation of codon choice across generations. This has the effect of eliminating the impact of spontaneous synonymous mutations, a key benefit of a redundant genetic code. As a result, non-synonymous mutations are the only DNA-level changes that are transmitted across generations, and, as non-synonymous mutations can emerge at both 'genotypic' and 'phenotypic' levels, these occur at a two-fold higher frequency than in a unidirectional system. Our system holds some practical insight. First, for DNA read/write systems, it may be wise to avoid designing systems with 'de novo reverse translation' because the opportunities for mutation are higher; tracking genotype information from the preceding generation to guide this process may reduce error. Second, our system helps clarify how a 'Lamarckian' biological system might operate. We conclude that, were a 'Lamarckian' system of inheritance a feature of early genetic systems, it would likely have been short lived as the high frequency of mutation would risk driving the system to extinction. A system based on unidirectional information flow thus appears superior as there are fewer opportunities for mutational error.

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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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