AI Article Synopsis

  • The activity of Mad1 at kinetochores is crucial for the spindle assembly checkpoint (SAC), which prevents anaphase from starting if kinetochores aren't properly attached to spindle fibers.
  • The RZZ complex (Rod, Zw10, Zwilch) is key for recruiting Mad1 to kinetochores, but how this happens isn't fully understood.
  • This study shows that while Mad1 has a dynamic presence at unattached kinetochores with a half-life of 12 seconds, RZZ remains stable, and there's a physical association between Mad1 and RZZ.

Article Abstract

The presence or absence of Mad1 at kinetochores is a major determinant of spindle assembly checkpoint (SAC) activity, the surveillance mechanism that delays anaphase onset if one or more kinetochores remain unattached to spindle fibers. Among the factors regulating the levels of Mad1 at kinetochores is the Rod, Zw10, and Zwilch (RZZ) complex, which is required for Mad1 recruitment through a mechanism that remains unknown. The relative dynamics and interactions of Mad1 and RZZ at kinetochores have not been extensively investigated, although Mad1 has been reported to be stably recruited to unattached kinetochores. In this study, we directly compare Mad1-green fluorescent protein (GFP) turnover dynamics on unattached Drosophila kinetochores with that of RZZ, tagged either with GFP-Rod or GFP-Zw10. We find that nearly 40 % of kinetochore-bound Mad1 has a significant dynamic component, turning over with a half-life of 12 s. RZZ in contrast is essentially stable on unattached kinetochores. In addition, we report that a fraction of RZZ and Mad1 can co-immunoprecipitate, indicating that the genetically determined recruitment hierarchy (in which Mad1 depends on RZZ) may reflect a physical association of the two complexes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469085PMC
http://dx.doi.org/10.1007/s10577-015-9472-xDOI Listing

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