Schild D, Byers B
Chromosoma. 1978 Dec 21;70(1):109-30. doi: 10.1007/BF00292220.
The meiotic effects of several cell division cycle (cdc) mutations of Saccharomyces cerevisiae have been investigated by electron microscopy and by genetic and biochemical methods. Diploid strains homozygous for cdc mutations known to confer defects on vegetative DNA synthesis were subjected to restrictive conditions during meiosis. Electron microscopy revealed that all four mutants were conditionally arrested in meiosis after duplication of the spindle pole bodies but before spindle formation for the first meiotic division. None of these mutants became committed to a recombination or contained synaptonemal complex at the meiotic arrest.--The mutants differed in their ability to undergo premeiotic DNA synthesis under restrictive conditions. Both cdc8 and cdc21, which are defective in the propagation of vegetative DNA synthesis, also failed to undergo premeiotic DNA synthesis. The arrest of these mutants at the stage before meiosis I spindle formation could be attributed to the failure of DNA synthesis because inhibition of synthesis by hydroxyurea also caused arrest at this stage.--Premeiotic DNA synthesis occurred before the arrest of cdc7, which is defective in the initiation of vegetative DNA synthesis, and of cdc2, which synthesizes vegetative DNA but does so defectively. The meiotic arrest of cdc7 homozygotes was partially reversible. Even if further semiconservative DNA replication was inhibited by the addition of hydroxyurea, released cells rapidly underwent commitment to recombination and formation of synaptonemal complexes. The cdc7 homozygote is therefore reversibly arrested in meiosis after DNA replication, whereas vegetative cultures have previously been shown to be defective only in the initation of DNA synthesis.
通过电子显微镜以及遗传学和生物化学方法,对酿酒酵母几种细胞分裂周期(cdc)突变的减数分裂效应进行了研究。已知对营养型DNA合成有缺陷的cdc突变纯合二倍体菌株在减数分裂期间处于限制条件下。电子显微镜显示,所有四个突变体在纺锤体极体复制后但在第一次减数分裂纺锤体形成之前的减数分裂中均受到条件性阻滞。这些突变体在减数分裂阻滞时均未进行重组或含有联会复合体。——这些突变体在限制条件下进行减数分裂前DNA合成的能力有所不同。在营养型DNA合成传播方面有缺陷的cdc8和cdc21,也未能进行减数分裂前DNA合成。这些突变体在减数分裂I纺锤体形成前阶段的阻滞可归因于DNA合成的失败,因为羟基脲对合成的抑制也导致在此阶段阻滞。——减数分裂前DNA合成发生在cdc7(在营养型DNA合成起始方面有缺陷)和cdc2(合成营养型DNA但有缺陷)阻滞之前。cdc7纯合子的减数分裂阻滞部分可逆。即使通过添加羟基脲进一步抑制半保留DNA复制,释放的细胞也会迅速进行重组并形成联会复合体。因此,cdc7纯合子在DNA复制后的减数分裂中可逆性阻滞,而营养型培养物此前已被证明仅在DNA合成起始方面有缺陷。