Impact of HERV-K expression on HIV-1 life cycle

描述：8%的人类基因组源自逆转录病毒。人类内源性逆转录病毒（HERV-K） RNA、蛋白质和病毒粒子已在癌症和HIV-1患者中检测到。大量证据表明，许多内源性逆转录病毒在HIV-1感染后表达上调。因此，HIV-1在人类细胞中的感染相当于几种逆转录病毒的共同感染。由于herv遭受负选择，大多数内源性逆转录病毒失去了复制能力。我们假设内源性逆转录病毒和HIV之间的相互作用影响外源性慢病毒感染和复制的结果。尽管人类基因组中至少有89种HERV-Ks，但它们通常被作为单一的原病毒进行研究。我们的目标是描述在感染HIV之前和之后存在于原代细胞中的HERV-K转录物的完整序列，并确定这些共感染如何改变细胞和病毒特性，如靶细胞易感性、病毒感染性和细胞趋向性。我们建议将最先进的深度测序技术与分子病毒学方法相结合，在分子水平上研究HIV/HERV-K相互作用。该方法将提供：HERV-K原代细胞的表达谱

DESCRIPTION: Eight percent of the human genome is of retroviral origin. Human endogenous retroviruses (HERV-K) RNA, proteins and virions have been detected in patients with cancer and HIV-1. There is abundant evidence that the expression of many endogenous retroviruses is up-regulated upon HIV-1 infection. Thus, HIV-1 infection in human cells is equivalent to a co-infection of several retroviruses. Because of the negative selection HERVs are subjected to, most of those endogenous retroviruses have lost their ability to replicate. We hypothesize that the interactions between endogenous retroviruses and HIV affect the outcome of exogenous the lentivirus infection and replication. Although there are at least 89 HERV-Ks in the human genome often they are studied as single provirus. Our objective is to delineate the full array of HERV-K transcripts present in primary cells prior as well as after infection with HIV, and determine how these co-infections change cellular and viral properties such as target cell susceptibility, viral infectivity and cell tropism. We propose to combine state-of-the-art deep sequencing technologies with molecular virology approaches to study HIV/HERV-K interactions at the molecular level. This approach will deliver: HERV-K expression profiling in primary cells in both infect and non-infected settings as well as the establishment of the impact that the relevant HERV-Ks have on the early late stages of the HIV life cycle.