Kassir Y, Simchen G
Genetics. 1978 Sep;90(1):49-68. doi: 10.1093/genetics/90.1.49.
Vegetative cells carrying the new temperature-sensitive mutation cdc40 arrest at the restrictive temperature with a medial nuclear division phenotype. DNA replication is observed under these conditions, but most cells remain sensitive to hydroxyurea and do not complete the ongoing cell cycle if the drug is present during release from the temperature block. It is suggested that the cdc40 lesion affects an essential function in DNA synthesis. Normal meiosis is observed at the permissive temperature in cdc40 homozygotes. At the restrictive temperature, a full round of premeiotic DNA replication is observed, but neither commitment to recombination nor later meiotic events occur. Meiotic cells that are already committed to the recombination process at the permissive temperature do not complete it if transferred to the restrictive temperature before recombination is realized. These temperature shift-up experiments demonstrate that the CDC40 function is required for the completion of recombination events, as well as for the earlier stage of recombination commitment. Temperature shift-down experiments with cdc40 homozygotes suggest that meiotic segregation depends on the final events of recombination rather than on commitment to recombination.
携带新的温度敏感突变cdc40的营养细胞在限制温度下停滞,呈现核内中间分裂表型。在这些条件下可观察到DNA复制,但大多数细胞对羟基脲仍敏感,并且如果在从温度阻滞释放期间存在该药物,则无法完成正在进行的细胞周期。这表明cdc40损伤影响DNA合成中的一个基本功能。在cdc40纯合子的允许温度下可观察到正常减数分裂。在限制温度下,可观察到一轮完整的减数分裂前DNA复制,但既不发生对重组的启动,也不发生后期减数分裂事件。在允许温度下已启动重组过程的减数分裂细胞,如果在重组实现之前转移到限制温度,则无法完成重组。这些温度上调实验表明,CDC40功能对于重组事件的完成以及重组启动的早期阶段都是必需的。对cdc40纯合子进行的温度下调实验表明,减数分裂分离取决于重组的最终事件,而不是对重组的启动。