进化上新近的转录因子参与人类细胞周期调控。

IF 11.1 Q1 CELL BIOLOGY
Cell genomics Pub Date : 2025-08-13 Epub Date: 2025-06-23 DOI:10.1016/j.xgen.2025.100923
Cyril Pulver, Romain Forey, Alex R Lederer, Martina Begnis, Olga Rosspopoff, Joana Carlevaro-Fita, Filipe Martins, Evarist Planet, Julien Duc, Charlène Raclot, Sandra Offner, Alexandre Coudray, Arianna Dorschel, Didier Trono
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引用次数: 0

摘要

细胞周期是真核生物生物学的一个基本过程,因此由一个高度保守的核心信号级联控制。然而,最近进化的蛋白质是否也影响这一过程尚不清楚。在这里,我们系统地绘制了进化上最近的转录因子(TFs)对人类细胞周期进程的影响。我们发现选择的年轻tf的基因组靶点,其中许多属于快速进化的kr ppel相关盒锌指蛋白(KZFP)家族,表现出同步的细胞周期表达。系统扰动研究表明,沉默最近的tf会破坏正常的细胞周期进程,我们在实验中证实了ZNF519(一种猿类限制性KZFP)的作用。此外,我们发现动物特异性KZFP ZNF274设定了数百个聚集基因的细胞周期表达和复制时间,其中许多是KZFP。这些发现强调了在细胞周期调节中谱系特异性未被充分认识的水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evolutionarily recent transcription factors partake in human cell cycle regulation.

The cell cycle is a fundamental process in eukaryotic biology and is accordingly controlled by a highly conserved core signaling cascade. However, whether recently evolved proteins also influence this process is unclear. Here, we systematically map the influence of evolutionarily recent transcription factors (TFs) on human cell cycle progression. We find that the genomic targets of select young TFs, many of which belong to the rapidly evolving Krüppel-associated box zinc-finger protein (KZFP) family, exhibit synchronized cell cycle expression. Systematic perturbation studies reveal that silencing recent TFs disrupts normal cell cycle progression, which we experimentally confirm for ZNF519, a simian-restricted KZFP. Furthermore, we show that the therian-specific KZFP ZNF274 sets the cell cycle expression and replication timing of hundreds of clustered genes, many of which are KZFPs. These findings highlight an underappreciated level of lineage specificity in cell cycle regulation.

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CiteScore
7.10
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