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真核生物的进化推断确定了塑造细胞器基因保留的普遍特征。

Evolutionary inference across eukaryotes identifies universal features shaping organelle gene retention.

机构信息

Department of Mathematics, University of Bergen, Bergen, Norway.

CNRS UMR7156, Génétique moléculaire, génomique, microbiologie (GMGM), Université de Strasbourg, Strasbourg, France.

出版信息

Cell Syst. 2022 Nov 16;13(11):874-884.e5. doi: 10.1016/j.cels.2022.08.007. Epub 2022 Sep 16.

Abstract

Mitochondria and plastids power complex life. Why some genes and not others are retained in their organelle DNA (oDNA) genomes remains a debated question. Here, we attempt to identify the properties of genes and associated underlying mechanisms that determine oDNA retention. We harness over 15k oDNA sequences and over 300 whole genome sequences across eukaryotes with tools from structural biology, bioinformatics, machine learning, and Bayesian model selection. Previously hypothesized features, including the hydrophobicity of a protein product, and less well-known features, including binding energy centrality within a protein complex, predict oDNA retention across eukaryotes, with additional influences of nucleic acid and amino acid biochemistry. Notably, the same features predict retention in both organelles, and retention models learned from one organelle type quantitatively predict retention in the other, supporting the universality of these features-which also distinguish gene profiles in more recent, independent endosymbiotic relationships. A record of this paper's transparent peer review process is included in the supplemental information.

摘要

线粒体和质体为复杂的生命提供动力。为什么有些基因而不是其他基因保留在它们的细胞器 DNA(oDNA)基因组中,这仍然是一个有争议的问题。在这里,我们试图确定决定 oDNA 保留的基因特性和相关潜在机制。我们利用来自结构生物学、生物信息学、机器学习和贝叶斯模型选择的工具,从 15k 多个 oDNA 序列和 300 多个真核生物全基因组序列中进行研究。以前假设的特征,包括蛋白质产物的疏水性,以及不太为人知的特征,包括蛋白质复合物中的结合能中心性,预测了真核生物中的 oDNA 保留,还受到核酸和氨基酸生物化学的影响。值得注意的是,相同的特征可以预测在两个细胞器中的保留,并且从一种细胞器类型中学习到的保留模型可以定量预测另一种细胞器中的保留,这支持了这些特征的普遍性——这些特征也可以区分最近独立的内共生关系中的基因特征。本论文的透明同行评审过程记录包含在补充信息中。

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