Ayusawa D, Shimizu K, Koyama H, Takeishi K, Seno T
J Biol Chem. 1983 Oct 25;258(20):12448-54.
Thymidylate synthase-negative mutants of cultured mouse cells were immediately committed to cell death upon thymidine deprivation, especially when the cells were synchronized in the S phase. Thymidylate deprivation induced single strand breaks in chromosome-size DNA strands, as measured by alkaline sucrose gradient sedimentation, giving rise to two peaks, one with large and the other with small fragments, the latter about the size of T4 DNA. An increase in the small DNA fragments paralleled that of thymineless death. Thymidine deprivation also produced double strand DNA fragments as determined by a method of neutral filter elution, and their extent paralleled that of cell death. Double-stranded DNA eluted through the filter sedimented as a single peak both in a neutral and in an alkaline sucrose gradient that coincided with that of the above small DNA fragments. Therefore, the strand breaks seemed to occur in some defined portions of the genome and in a specific manner compared to breaks induced by x-rays, which occurred rather randomly. Cycloheximide blocked both thymineless death and the production of the small DNA fragments. The strand breaks induced by thymidine starvation were not repaired but instead advanced on subsequent incubation of the cells in growth medium containing thymidine.
培养的小鼠细胞胸苷酸合成酶阴性突变体在胸腺嘧啶核苷剥夺后立即走向细胞死亡,尤其是当细胞同步于S期时。通过碱性蔗糖梯度沉降法测定,胸腺嘧啶核苷剥夺诱导染色体大小的DNA链出现单链断裂,产生两个峰,一个峰含有大片段,另一个峰含有小片段,后者大小约为T4 DNA。小DNA片段的增加与无胸腺嘧啶死亡平行。通过中性滤膜洗脱法测定,胸腺嘧啶核苷剥夺还产生双链DNA片段,其程度与细胞死亡平行。通过滤膜洗脱的双链DNA在中性和碱性蔗糖梯度中均以单峰形式沉降,这与上述小DNA片段的峰一致。因此,与X射线诱导的随机断裂相比,这些链断裂似乎以特定方式发生在基因组的某些特定区域。放线菌酮可阻断无胸腺嘧啶死亡和小DNA片段的产生。胸腺嘧啶核苷饥饿诱导的链断裂未被修复,而是在随后将细胞置于含胸腺嘧啶核苷的生长培养基中培养时进一步发展。