解开进化背后的细胞内在和细胞外在因素。

IF 11.1 Q1 CELL BIOLOGY
Cell genomics Pub Date : 2025-08-13 Epub Date: 2025-05-29 DOI:10.1016/j.xgen.2025.100891
Alexander L Starr, Toshiya Nishimura, Kyomi J Igarashi, Chihiro Funamoto, Hiromitsu Nakauchi, Hunter B Fraser
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引用次数: 0

摘要

生物学中一个长期存在的问题是,细胞在多大程度上是自主运作的,而不是需要与其他细胞或环境因素相互作用。在这里,我们开发了一个使用种间嵌合体的框架,以精确地将任何细胞特征的进化分歧分解为细胞内在和细胞外在成分。将这一框架应用于互惠大鼠-小鼠嵌合体中数千个基因表达水平,我们发现大多数分化是细胞内在的,尽管外在因素也起着不可或缺的作用。例如,转录因子的细胞外源性调控可以传播到其靶基因,导致细胞类型特异性的mRNA和蛋白质水平的外源性调控。我们还发现,在嵌合体中,印迹基因显著地错误表达,这表明在快速进化的内在和外在印迹机制之间存在不匹配。总的来说,我们的概念框架为研究任何多细胞生物中无数细胞特征的进化、发展和调节的机制基础开辟了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Disentangling cell-intrinsic and cell-extrinsic factors underlying evolution.

A long-standing question in biology is the extent to which cells function autonomously as opposed to requiring interactions with other cells or environmental factors. Here, we develop a framework to use interspecies chimeras to precisely decompose evolutionary divergence in any cellular trait into cell-intrinsic and cell-extrinsic components. Applying this framework to thousands of gene expression levels in reciprocal rat-mouse chimeras, we found that most divergence is cell intrinsic, though extrinsic factors also play an integral role. For example, cell-extrinsic regulation of a transcription factor can propagate to its target genes, leading to cell-type-specific extrinsic regulation of both their mRNA and their protein levels. We also show that imprinted genes are dramatically misexpressed in chimeras, suggesting a mismatch between rapidly evolving intrinsic and extrinsic imprinting mechanisms. Overall, our conceptual framework opens up new avenues to investigate the mechanistic basis of the evolution, development, and regulation of myriad cellular traits in any multicellular organism.

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CiteScore
7.10
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