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Fast and efficient generation of knock-in human organoids using homology-independent CRISPR-Cas9 precision genome editing.利用同源非依赖的 CRISPR-Cas9 精准基因组编辑技术快速有效地生成基因敲入人类类器官。
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p53 mitotic centrosome localization preserves centrosome integrity and works as sensor for the mitotic surveillance pathway.p53 有丝分裂中心体定位可保持中心体的完整性,并作为有丝分裂监控途径的传感器。
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Hypo-osmotic-like stress underlies general cellular defects of aneuploidy.低渗样应激是非整倍体细胞普遍缺陷的基础。
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Genomic and Functional Approaches to Understanding Cancer Aneuploidy.基因组和功能方法研究癌症非整倍性。
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Cellular Stress Associated with Aneuploidy.细胞非整倍体相关的应激反应。
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Three-dimensional organotypic culture: experimental models of mammalian biology and disease.三维器官型培养:哺乳动物生物学与疾病的实验模型
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Mitotic Kinases and p53 Signaling.有丝分裂激酶与p53信号传导
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10
Proliferation of aneuploid human cells is limited by a p53-dependent mechanism.人类非整倍体细胞的增殖受到依赖 p53 的机制的限制。
J Cell Biol. 2010 Feb 8;188(3):369-81. doi: 10.1083/jcb.200905057. Epub 2010 Feb 1.

p53 与染色体稳定性之间的复杂相互作用。

Complex interplay between p53 and chromosome stability.

作者信息

Narkar Akshay, Johnson Blake A, Li Rong

机构信息

Center for Cell Dynamics and Department of Cell Biology, Johns Hopkins University, School of Medicine, Baltimore, MD, USA.

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Mol Cell Oncol. 2021 Jun 28;8(4):1938479. doi: 10.1080/23723556.2021.1938479. eCollection 2021.

DOI:10.1080/23723556.2021.1938479
PMID:34616871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8489959/
Abstract

TP53-dependent cell cycle arrest has been proposed to limit the proliferation of aneuploid cells. We investigated the cellular response to aneuploidy in cell lines and organoid cultures and found that TP53 (also known as p53) is not activated following aneuploidy induction in organoids. However, we confirmed that p53 is required for high mitotic fidelity. Our findings provide a revised view on how p53 safeguards against aneuploidy.

摘要

有人提出,依赖TP53的细胞周期阻滞可限制非整倍体细胞的增殖。我们研究了细胞系和类器官培养物对非整倍体的细胞反应,发现类器官中诱导非整倍体后TP53(也称为p53)未被激活。然而,我们证实p53是高有丝分裂保真度所必需的。我们的研究结果为p53如何防止非整倍体提供了一个新的观点。