Schwartz S, Felber B K, Benko D M, Fenyö E M, Pavlakis G N
Department of Virology, School of Medicine, Karolinska Institute, Stockholm, Sweden.
J Virol. 1990 Jun;64(6):2519-29. doi: 10.1128/JVI.64.6.2519-2529.1990.
We have used the polymerase chain reaction technique to clone the small multiply spliced mRNA species produced after infection of human cells by a molecular clone of human immunodeficiency virus type 1 (HIV-1). We identified six Rev-expressing mRNAs, which were generated by the use of two splice acceptors located immediately upstream of the rev AUG. The class of small mRNAs included 12 mRNAs expressing Tat, Rev, and Nef. In addition, HIV-1 produced other multiply spliced mRNAs that used alternative splice sites identified by cloning and sequencing. All of these mRNAs were found in the cytoplasm and should be able to produce additional proteins. The coding capacity of the tat, rev, and nef mRNAs was analyzed by transfection of the cloned cDNAs into human cells. The tat mRNAs produced high levels of Tat, but very low levels of Rev and Nef. All the rev mRNAs expressed high levels of both Rev and Nef and were essential for the production of sufficient amounts of Rev. Therefore, HIV-1 uses both alternatively spliced and bicistronic mRNAs for the production of Tat, Rev, and Nef proteins.
我们运用聚合酶链反应技术,克隆了人类免疫缺陷病毒1型(HIV-1)分子克隆感染人类细胞后产生的多种小的经剪接的mRNA种类。我们鉴定出六种表达Rev的mRNA,它们是通过利用位于rev AUG上游紧邻位置的两个剪接受体产生的。这类小mRNA包括12种表达Tat、Rev和Nef的mRNA。此外,HIV-1产生了其他多种经剪接的mRNA,这些mRNA利用了通过克隆和测序鉴定出的可变剪接位点。所有这些mRNA都存在于细胞质中,并且应该能够产生额外的蛋白质。通过将克隆的cDNA转染到人类细胞中,分析了tat、rev和nef mRNA的编码能力。tat mRNA产生高水平的Tat,但Rev和Nef的水平非常低。所有的rev mRNA都高水平表达Rev和Nef,并且对于产生足够量的Rev至关重要。因此,HIV-1利用可变剪接的mRNA和双顺反子mRNA来产生Tat、Rev和Nef蛋白。