PT - JOURNAL ARTICLE AU - Mohammed Abdullahel Amin AU - Destiny Ariel Wallace AU - Dileep Varma TI - The Ndc80 complex is essential for the initial kinetochore-microtubule capture during early mitosis AID - 10.1101/2022.02.10.479964 DP - 2022 Jan 01 TA - bioRxiv PG - 2022.02.10.479964 4099 - http://biorxiv.org/content/early/2022/02/10/2022.02.10.479964.short 4100 - http://biorxiv.org/content/early/2022/02/10/2022.02.10.479964.full AB - Mitotic kinetochores are initially captured by dynamic microtubules via a ‘search-and-capture’ mechanism. The microtubule motor, dynein, is critical for kinetochore capture as it has been shown to transport microtubule-attached chromosomes towards the spindle pole during early mitosis. In metaphase, the kinetochore localized, microtubule-binding complex, Ndc80, plays a central role in stabilizing kinetochore-microtubule (kMT) attachments. It is not yet clear, however, if Ndc80, which is recruited to kinetochores very early during mitosis contributes to initial kMT capture. Here, by combining CRISPR/Cas9-mediated knockout and RNAi technology with assays specifically targeted to study kMT capture, we show that mitotic cells lacking Ndc80 exhibit severe defects in this function during prometaphase. Rescue experiments show that Ndc80 mutants deficient in microtubule-binding are unable to execute proper kMT capture. While cells inhibited of dynein alone are predominantly able to make initial kMT attachments, cells co-depleted of Ndc80 and dynein show severe defects in kMT capture. Further, we demonstrate a novel physical interaction between Ndc80 and dynein during prometaphase. Thus, our studies, for the first time, identify a distinct event in the formation of initial kMT attachments, which is directly mediated by Ndc80 followed by a coordinated function with dynein, both of which are required for efficient kMT capture and proper chromosome alignment.Competing Interest StatementThe authors have declared no competing interest.DICDynein intermediate chainkMTkinetochore-microtubuleNdc80nuclear division cycle 80CENP-ECentrosome-associated protein EACA (CREST)anti-centromere antiserumsiRNAsmall interfering RNARNAiRNA interferenceKMNKnl1-Mis12-Ndc80CHcalponin homologySTLCS-Trityl-L-CysteineHec1Highly expressed in cancer protein 1CLIP-170CAP-GLY domain containing linker protein 170;