Müller W E, Schröder H C
Institute for Physiological Chemistry, University, Mainz, Germany.
Int J Sports Med. 1991 Jun;12 Suppl 1:S43-9. doi: 10.1055/s-2007-1024749.
HTLV-I, II, HIV-1, 2 and other retroviruses possess genes for the transcriptional activators, tax and tat, the expression of which is closely related with the pathogenesis of leukemia and human immunodeficiency syndrome (AIDS) and induced by the virus infection. The effects of these activators on the expression of host cell genes, however, are still largely unknown. Recently the authors have discovered that infection with HIV or Mo-MuLV causes a specific acceleration of the synthesis of an UAG suppressor glutamine tRNA in the host cell; they could demonstrate that this phenomenon is based on transcriptional promotion of tRNA genes which is due to a new transcriptional activator synthesized as a function of viral infection and/or increased virus levels. The present paper discusses the significance of the suppressor tRNA and explains the role of the virus in the regulation of its expression.
人类嗜T淋巴细胞病毒I型、II型、人类免疫缺陷病毒1型、2型及其他逆转录病毒都拥有转录激活因子tax和tat的基因,它们的表达与白血病和人类免疫缺陷综合征(艾滋病)的发病机制密切相关,且由病毒感染诱导产生。然而,这些激活因子对宿主细胞基因表达的影响在很大程度上仍不明确。最近,作者发现感染HIV或莫洛尼鼠白血病病毒(Mo-MuLV)会导致宿主细胞中一种UAG抑制性谷氨酰胺tRNA的合成特异性加速;他们能够证明这种现象是基于tRNA基因的转录促进,这是由于病毒感染和/或病毒水平升高而合成的一种新的转录激活因子所致。本文讨论了抑制性tRNA的意义,并解释了病毒在其表达调控中的作用。