Nocentini S, Moreno G, Coppey J
Mutat Res. 1980 Apr;70(2):231-4. doi: 10.1016/0027-5107(80)90163-3.
Separate cultures of CV-1 cells were exposed for 15 min to 1-16 mM formaldehyde (FA) at various time intervals before labeling with [3H]uridine. The labeled RNA extracted from whole cells was analyzed by polyacrylamide gel electrophoresis. Results indicated that FA produced transcription-terminating lesions in DNA which depressed RNA synthesis, gave rise to shortened RNA chains and modified the expression of transcription-linked genes. These lesions were efficiently repaired since a recovery of RNA transcription, with disappearance of the initially observed alterations, rapidly occurred during post-treatment incubation of cells. Cycloheximide (5 micrograms/ml) strongly inhibited this recovery, whereas fluorodeoxyuridine (10(-5) M) was without effect. The rate of semi-conservative DNA synthesis, measured autoradiographically by thymidine incorporation, as well as the number of cells performing DNA replication, fell to zero after 15-min exposure to FA concentrations greater than 2 mM. Both parameters recovered subnormal levels during a 24-h incubation after treatment with FA concentration up to 8 mM, in agreement with the high survival observed. Unscheduled DNA synthesis was not detectable during the restoration of DNA and RNA synthesis.
在以[³H]尿苷标记之前,将CV - 1细胞的单独培养物在不同时间间隔用1 - 16 mM甲醛(FA)处理15分钟。从全细胞中提取的标记RNA通过聚丙烯酰胺凝胶电泳进行分析。结果表明,FA在DNA中产生转录终止损伤,抑制RNA合成,导致RNA链缩短并改变转录相关基因的表达。这些损伤能够被有效修复,因为在细胞处理后的孵育过程中,RNA转录迅速恢复,最初观察到的改变消失。环己酰亚胺(5微克/毫升)强烈抑制这种恢复,而氟脱氧尿苷(10⁻⁵ M)则没有作用。通过胸苷掺入放射自显影法测量的半保留DNA合成速率以及进行DNA复制的细胞数量,在暴露于大于2 mM的FA 15分钟后降至零。在用高达8 mM的FA处理后的24小时孵育期间,这两个参数都恢复到低于正常水平,这与观察到的高存活率一致。在DNA和RNA合成恢复期间未检测到非预定DNA合成。