Shows hSpindly modulates SAC signaling in cells, suggesting a target for overcoming drug resistance.
The spindle assembly checkpoint (SAC) prevents sister chromatids separation until all chromosomes are properly attached to spindle microtubules and bi-oriented. SAC controls the metaphase-to-anaphase transition by inhibiting the anaphase promoting complex/cyclosome (APC/C). A critical step in this process is the recruitment of the Mad1-Mad2 complex to unattached kinetochores mediated by the KBB pathway (KNL1-Bub3-Bub1) and the RZZ pathway (Rod-Zw10-Zwilch). Here, we show that hSpindly contributes to the regulation of Mad1-Mad2 recruitment through the RZZ pathway. We demonstrate that hSpindly is a dynamic protein that oligomerizes at unattached kinetochores, and we identify threonine 552 as a key residue controlling its mobility and function. A non-phosphorylatable mutant (T552A) displays reduced dynamics at kinetochores, impairs SAC signaling, and increases cellular resistance to antimitotic drugs. Altogether, our findings identify hSpindly as a dynamic regulator of SAC signaling and potential therapeutic target for overcoming resistance to mitotic inhibitors.
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Mora‐Santos et al. (2026) studied this question.
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