Non-canonical role for the BAF complex subunit DPF3 in mitosis and ciliogenesis

被引:0
|
作者
Verrillo, Giulia [1 ]
Obeid, Anna Maria [1 ]
Genco, Alexia [1 ]
Scrofani, Jacopo [2 ]
Orange, Francois [3 ]
Hanache, Sarah [1 ]
Mignon, Julien [4 ]
Leyder, Tanguy [4 ]
Michaux, Catherine [4 ]
Kempeneers, Celine [5 ,6 ]
Bricmont, Noemie [5 ,6 ]
Herkenne, Stephanie [7 ]
Vernos, Isabelle [2 ,8 ,9 ]
Martin, Maud [10 ]
Mottet, Denis [1 ]
机构
[1] Univ Liege, GIGA Res Inst, Mol Anal Gene Express MAGE Lab, B34 Ave Hop, B-4000 Liege, Belgium
[2] Barcelona Inst Sci & Technol, Ctr Genom Regulat CRG, Barcelona 08003, Spain
[3] Univ Cote Azur, Ctr Commun Microscopie Appl CCMA, F-06100 Nice, France
[4] Univ Namur, Lab Phys Chem Biomol, Unite Chim Phys Theor & Struct UCPTS, Rue Bruxelles 61, B-5000 Namur, Belgium
[5] Univ Liege, GIGA Res Ctr, Pneumol Lab, I3 Grp, B-4000 Liege, Belgium
[6] Univ Hosp Liege, Dept Pediat, Div Respirol, B-4000 Liege, Belgium
[7] Univ Liege, Lab Mitochondria & Cell Commun, GIGA Canc, B34 Ave Hop, B-4000 Liege, Belgium
[8] Univ Pompeu Fabra UPF, Barcelona 08002, Spain
[9] ICREA, Pg Lluis Co 23, Barcelona 08010, Spain
[10] Univ Libre Bruxelles, ULB Neurosci Inst, Dept Mol Biol, Lab Neurovasc Signaling, B-6041 Gosselies, Belgium
关键词
DPF3; Chromosome alignment; Bridging fiber; Mitosis; Genomic instability; Centriolar satellites; Ciliogenesis; CHROMATIN REMODELING COMPLEX; RANGTP-DEPENDENT MAP; CHROMOSOME ALIGNMENT; PHASE-SEPARATION; CELL-CYCLE; PHOSPHORYLATION; KINETOCHORE; PROTEIN; ASSOCIATION; CENTROSOME;
D O I
10.1242/jcs.261744
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
DPF3, along with other subunits, is a well-known component of the BAF chromatin remodeling complex, which plays a key role in regulating chromatin remodeling activity and gene expression. Here, we elucidated a non-canonical localization and role for DPF3. We showed that DPF3 dynamically localizes to the centriolar satellites in interphase and to the centrosome, spindle midzone and bridging fiber area, and midbodies during mitosis. Loss of DPF3 causes kinetochore fiber instability, unstable kinetochore-microtubule attachment and defects in chromosome alignment, resulting in altered mitotic progression, cell death and genomic instability. In addition, we also demonstrated that DPF3 localizes to centriolar satellites at the base of primary cilia and is required for ciliogenesis by regulating axoneme extension. Taken together, these findings uncover a moonlighting dual function for DPF3 during mitosis and ciliogenesis.
引用
收藏
页数:19
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