da Costa Carvalho M G, Fournier M V
Lab. do Controle da Expressão Gênica, Instituto de Biofisica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Brazil.
Res Virol. 1991 Jan-Feb;142(1):25-31. doi: 10.1016/0923-2516(91)90024-w.
Three major Mayaro virus proteins of 62, 50 and 34 kDa were detected in Aedes albopictus cells after 48 h postinfection at 28 degrees C. When the infected cells were shifted from 28 to 37 degrees C for 90 min (heat shock conditions), the synthesis of two major heat shock proteins (HSP) 82 and 70 kDa was induced concomitantly with strong inhibition of virus and normal protein synthesis. Total cellular RNA was isolated from mock and infected cells incubated at 28 degrees C or under heat shock. Northern blot analysis with HSP genomic probes from Drosophila sp showed that (1) the probe for HSP 82 hybridized with an RNA of 2.6 kb present only in heat-shocked cells, (2) the HSP 70 probe hybridized with RNA species of 2.5 kb, present only in RNA from heat-shocked cells. These results showed that Mayaro virus was not able to alter the reprogrammation of gene expression induced by heat shock in A. albopictus cells.
在28摄氏度感染后48小时,在白纹伊蚊细胞中检测到分子量为62、50和34千道尔顿的三种主要马亚罗病毒蛋白。当感染细胞在28摄氏度转移至37摄氏度90分钟(热休克条件)时,两种主要热休克蛋白(HSP)82和70千道尔顿的合成被诱导,同时病毒和正常蛋白质合成受到强烈抑制。从在28摄氏度或热休克条件下培养的 mock 细胞和感染细胞中分离总细胞RNA。用果蝇属的HSP基因组探针进行Northern印迹分析表明:(1)HSP 82探针与仅存在于热休克细胞中的2.6 kb RNA杂交;(2)HSP 70探针与仅存在于热休克细胞RNA中的2.5 kb RNA种类杂交。这些结果表明,马亚罗病毒不能改变热休克诱导的白纹伊蚊细胞中基因表达的重编程。