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Artikel ; Online: Genomic instability caused by Arp2/3 complex inactivation results in micronucleus biogenesis and cellular senescence.

Haarer, Elena L / Theodore, Corey J / Guo, Shirley / Frier, Ryan B / Campellone, Kenneth G

PLoS genetics

2023  Band 19, Heft 1, Seite(n) e1010045

Abstract: The Arp2/3 complex is an actin nucleator with well-characterized activities in cell morphogenesis and movement, but its roles in nuclear processes are relatively understudied. We investigated how the Arp2/3 complex affects genomic integrity and cell ... ...

Abstract The Arp2/3 complex is an actin nucleator with well-characterized activities in cell morphogenesis and movement, but its roles in nuclear processes are relatively understudied. We investigated how the Arp2/3 complex affects genomic integrity and cell cycle progression using mouse fibroblasts containing an inducible knockout (iKO) of the ArpC2 subunit. We show that permanent Arp2/3 complex ablation results in DNA damage, the formation of cytosolic micronuclei, and cellular senescence. Micronuclei arise in ArpC2 iKO cells due to chromatin segregation defects during mitosis and premature mitotic exits. Such phenotypes are explained by the presence of damaged DNA fragments that fail to attach to the mitotic spindle, abnormalities in actin assembly during metaphase, and asymmetric microtubule architecture during anaphase. In the nuclei of Arp2/3-depleted cells, the tumor suppressor p53 is activated and the cell cycle inhibitor Cdkn1a/p21 mediates a G1 arrest. In the cytosol, micronuclei are recognized by the DNA sensor cGAS, which is important for stimulating a STING- and IRF3-associated interferon response. These studies establish functional requirements for the mammalian Arp2/3 complex in mitotic spindle organization and genome stability. They also expand our understanding of the mechanisms leading to senescence and suggest that cytoskeletal dysfunction is an underlying factor in biological aging.
Mesh-Begriff(e) Animals ; Mice ; Actin-Related Protein 2-3 Complex/genetics ; Actin-Related Protein 2-3 Complex/metabolism ; Actins/metabolism ; Cellular Senescence/genetics ; DNA/metabolism ; Genomic Instability/genetics ; Mitosis/genetics
Chemische Substanzen Actin-Related Protein 2-3 Complex ; Actins ; DNA (9007-49-2)
Sprache Englisch
Erscheinungsdatum 2023-01-27
Erscheinungsland United States
Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural
ZDB-ID 2186725-2
ISSN 1553-7404 ; 1553-7390
ISSN (online) 1553-7404
ISSN 1553-7390
DOI 10.1371/journal.pgen.1010045
Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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