Shimura M, Onozuka Y, Yamaguchi T, Hatake K, Takaku F, Ishizaka Y
Department of Intractable Diseases, International Medical Center of Japan, Tokyo.
Cancer Res. 1999 May 15;59(10):2259-64.
Vpr, an accessory gene of human immunodeficiency virus, induces cell cycle abnormality by accumulating cells at the G2-M phase. We reported recently that Vpr caused both micronuclei formation and aneuploidy. Here, we show that Vpr also induced chromosome breaks and gene amplification. Expression of Vpr induced more than 10-fold increase of colonies resistant to N-(phosphonacetyl)-L-aspartate, an inhibitor of pyrimidine de novo synthesis. Fluorescence in situ hybridization analysis detected that 4 of 10 N-(phosphonacetyl)-L-aspartate resistant clones studied had intrachromosomal amplification of carbamyl-phosphate synthetase/aspartate transcarbamoylase/dihydroorotase gene. Another single clone had dicentrics. Data suggested that the Vpr-induced chromosome breaks leading to gene amplification, followed by bridge-breakage-fusion cycle, were one of the possible mechanisms of Vpr-induced genomic instability.
Vpr是人类免疫缺陷病毒的一个辅助基因,它通过使细胞在G2-M期积累来诱导细胞周期异常。我们最近报道,Vpr会导致微核形成和非整倍体。在此,我们表明Vpr还会诱导染色体断裂和基因扩增。Vpr的表达使对嘧啶从头合成抑制剂N-(膦酰乙酰基)-L-天冬氨酸耐药的菌落增加了10倍以上。荧光原位杂交分析检测到,在研究的10个对N-(膦酰乙酰基)-L-天冬氨酸耐药的克隆中,有4个具有氨甲酰磷酸合成酶/天冬氨酸转氨甲酰酶/二氢乳清酸酶基因的染色体内扩增。另一个单一克隆有双着丝粒。数据表明,Vpr诱导的染色体断裂导致基因扩增,随后是桥-断裂-融合循环,这是Vpr诱导基因组不稳定的可能机制之一。