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SNM1B/Apollo interacts with astrin and is required for the prophase cell cycle checkpoint.
- Source :
-
Cell cycle (Georgetown, Tex.) [Cell Cycle] 2009 Feb 15; Vol. 8 (4), pp. 628-38. Date of Electronic Publication: 2009 Feb 07. - Publication Year :
- 2009
-
Abstract
- Previously, we have shown that SNM1A is a multifunctional gene involved in both the DNA damage response and in an early mitotic checkpoint in response to spindle stress. Another member of the SNM1 gene family, SNM1B/Apollo, has been shown to have roles in both the response to DNA interstrand cross-linking agents and in telomere protection during S phase. Here, we demonstrate a novel role for SNM1B/Apollo in mitosis in response to spindle stress. SNM1B-deficient cells exhibit a defect in the prophase checkpoint. Loss of the prophase checkpoint induces an extended mitotic delay, which is due to prolonged activation of the spindle checkpoint. In addition, we show that SNM1B/Apollo interacts with the essential microtubule binding protein Astrin. SNM1B/Apollo interacts with Astrin through its conserved metallo-beta-lactamase domain, and disruption of this interaction by point mutations results in a deficient prophase checkpoint. These findings suggest that SNM1B/Apollo and Astrin function together to enforce the prophase checkpoint in response to spindle stress.
- Subjects :
- Animals
Cell Cycle Proteins genetics
Cell Line
Centrosome metabolism
DNA Repair Enzymes genetics
Exodeoxyribonucleases
Humans
Nocodazole metabolism
Nuclear Proteins genetics
Recombinant Fusion Proteins genetics
Recombinant Fusion Proteins metabolism
Spindle Apparatus
Tubulin Modulators metabolism
Two-Hybrid System Techniques
Cell Cycle Proteins metabolism
DNA Repair Enzymes metabolism
Nuclear Proteins metabolism
Prophase physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1551-4005
- Volume :
- 8
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Cell cycle (Georgetown, Tex.)
- Publication Type :
- Academic Journal
- Accession number :
- 19197158
- Full Text :
- https://doi.org/10.4161/cc.8.4.7791