Gametes are produced via meiosis, a specialized cell division associated with frequent errors that cause birth defects and infertility. Uniquely in meiosis I, homologous chromosomes segregate to opposite poles, usually requiring their linkage by chiasmata, the products of crossover recombination.¹ The spindle checkpoint delays cell-cycle progression until all chromosomes are properly attached to microtubules,² but the steps leading to the capture and alignment of chromosomes on the meiosis I spindle remain poorly understood. In budding yeast meiosis I, Mad2 and Mad3^BUBR1 are equally important for spindle checkpoint delay, but biorientation of homologs on the meiosis I spindle requires Mad2, but not Mad3^BUBR1.^3,4 Here we reveal the distinct functions of Mad2 and Mad3^BUBR1 in meiosis I chromosome segregation. Mad2 promotes the prophase to metaphase I transition, while Mad3^BUBR1 associates with the TOGL1 domain of Stu1^CLASP, a conserved plus-end microtubule protein that is important for chromosome capture onto the spindle. Homologous chromosome pairs that are proficient in crossover formation but fail to biorient rely on Mad3^BUBR1-Stu1^CLASP to ensure their efficient attachment to microtubules and segregation during meiosis I. Furthermore, we show that Mad3^BUBR1-Stu1^CLASP are essential to rescue the segregation of mini-chromosomes lacking crossovers. Our findings define a new pathway ensuring microtubule-dependent chromosome capture and demonstrate that spindle checkpoint proteins safeguard the fidelity of chromosome segregation both by actively promoting chromosome alignment and by delaying cell-cycle progression until this has occurred.

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Journal Article

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Mukherjee A, Spanos C, Marston AL

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