Flygare J, Benson F, Hellgren D
Department of Bioscience at Novum, Karolinska Institutet, Huddinge, Sweden.
Biochim Biophys Acta. 1996 Jul 24;1312(3):231-6. doi: 10.1016/0167-4889(96)00040-7.
The S. cerevisiae RAD51 gene product exerts important functions in meiotic and mitotic recombination, as well as in the repair of DNA double-strand breaks. We have studied the expression of the human RAD51 (HsRAD51) gene in primary human peripheral blood lymphocytes (PBLs). The HsRAD51 mRNA level increased three fold in mitogen stimulated PBLs, with a peak in the late S phase. A five fold increase of HsRAD51 protein levels was observed in late G2. Specific inhibition of DNA synthesis with aphidicolin did not block the induction of the HsRAD51 protein, indicating that HsRAD51 expression is independent of DNA replication. In contrast, after inhibition of RNA synthesis with actinomycin D and protein synthesis with cycloheximide, the HsRAD51 protein level decreased rapidly. Taken together, these results indicate that the HsRAD51 gene is transcriptionally regulated in human PBLs, and exerts its function during the late S and G2 phases of the cell cycle.
酿酒酵母RAD51基因产物在减数分裂和有丝分裂重组以及DNA双链断裂修复中发挥重要作用。我们研究了人类RAD51(HsRAD51)基因在原代人外周血淋巴细胞(PBL)中的表达。在有丝分裂原刺激的PBL中,HsRAD51 mRNA水平增加了三倍,在S期后期达到峰值。在G2期后期观察到HsRAD51蛋白水平增加了五倍。用阿非迪霉素特异性抑制DNA合成并未阻断HsRAD51蛋白的诱导,表明HsRAD51表达独立于DNA复制。相反,在用放线菌素D抑制RNA合成并用环己酰亚胺抑制蛋白质合成后,HsRAD51蛋白水平迅速下降。综上所述,这些结果表明HsRAD51基因在人PBL中受到转录调控,并在细胞周期的S期后期和G2期发挥其功能。