Esqueda Daniel, Xu Fangling, Moore Yuliana, Yang Zhen, Huang Gengming, Lennon Patrick A, Hu Peter C, Dong Jianli
Molecular Genetic Technology Program, School of Health Sciences, University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Ann Clin Lab Sci. 2013 Spring;43(2):122-5.
HERV-K viral RNA has been reported in plasma specimens of HIV-1 infected individuals. Emerging data support the regulation and functional interaction between HERV-K and HIV-1, which warrant development of accurate HERV-K assays to evaluate HERV-K activation. In this study, we examined HERV-K RNA expression after careful removal of "contaminating" cellular DNA using DNase I. We found that DNase I digestion effectively reduced HERV-K RT-PCR positive signal. We also found that levels of HERV-K expression did not correlate with HIV-1 viral load. Our study is in agreement with the published studies on HERV-K activation in HIV-1 positive plasma specimens, and in addition, calls for careful removal of cellular DNA to accurately evaluate HERV-K RNA expression.
在HIV-1感染者的血浆样本中已报道存在人内源性逆转录病毒K(HERV-K)病毒RNA。新出现的数据支持HERV-K与HIV-1之间的调控及功能相互作用,这就需要开发准确的HERV-K检测方法来评估HERV-K的激活情况。在本研究中,我们使用脱氧核糖核酸酶I(DNase I)仔细去除“污染性”细胞DNA后,检测了HERV-K RNA的表达。我们发现DNase I消化有效降低了HERV-K逆转录聚合酶链反应(RT-PCR)阳性信号。我们还发现HERV-K的表达水平与HIV-1病毒载量无关。我们的研究与已发表的关于HIV-1阳性血浆样本中HERV-K激活的研究结果一致,此外,还要求仔细去除细胞DNA以准确评估HERV-K RNA的表达。