Farrington G K, Lynch P, Jensen A, Böhnlein E, Doten R, Maione T, Daly T, Rusche J
Repligen Corporation, Cambridge, MA 02139.
Adv Exp Med Biol. 1991;303:15-22. doi: 10.1007/978-1-4684-6000-1_2.
These studies demonstrate that HIV-1 REV and HTLV-1 REX are site specific RNA binding proteins. In addition, the REV protein studies indicate a protein domain essential for biological function that is not involved in RRE binding. Lentiviruses are unique among retroviruses in providing gene products to switch expression from early to late genes. Rather than transcriptional control, this is accomplished by regulating RNA transport. A further understanding of these lentiviral genes may identify means of inhibiting viruses responsible for insidious human disease.
这些研究表明,HIV-1 REV和HTLV-1 REX是位点特异性RNA结合蛋白。此外,对REV蛋白的研究表明,存在一个对生物学功能至关重要但不参与RRE结合的蛋白结构域。慢病毒在逆转录病毒中独具特色,它能提供基因产物以实现从早期基因到晚期基因的表达转换。这一过程并非通过转录控制,而是通过调节RNA转运来完成。对这些慢病毒基因的进一步了解可能会找到抑制引发隐匿性人类疾病的病毒的方法。