Benko D M, Schwartz S, Pavlakis G N, Felber B K
National Cancer Institute-Frederick Cancer Research Facility, Maryland 21701-1013.
J Virol. 1990 Jun;64(6):2505-18. doi: 10.1128/JVI.64.6.2505-2518.1990.
We have characterized a novel 28-kilodalton protein, p28tev, detected in human immunodeficiency virus type 1-infected cells. tev is recognized by both tat and rev monospecific antibodies. tev is initiated at the tat AUG and contains the first exon of tat at its amino terminus, a small portion of env in the middle, and the second exon of rev at its carboxy terminus. A cDNA clone producing tev was cloned and expressed in human cells. Sequence analysis revealed that the tev mRNA is generated by splicing to a novel exon located in the env region. This identifies a fourth class of multiply spliced human immunodeficiency virus mRNAs, produced in infected and transfected cells. tev is regulated during the virus life cycle similarly to the other regulatory proteins, tat, rev, and nef, and displays both tat and rev activities in functional assays. Since tev contains important functional domains of tat and rev and is produced very early after transfection, it may be an important regulator in the initial phase of virus expression. Another rev-related protein, p18(6)Drev, containing env and rev sequences, was characterized and was found not to have detectable rev activity.
我们已鉴定出一种在1型人类免疫缺陷病毒感染细胞中检测到的新型28千道尔顿蛋白p28tev。tev可被tat和rev单特异性抗体识别。tev由tat的AUG起始,其氨基末端包含tat的第一个外显子,中间有一小部分env,羧基末端包含rev的第二个外显子。产生tev的cDNA克隆被克隆并在人类细胞中表达。序列分析表明,tev mRNA是通过剪接至env区域中的一个新外显子产生的。这确定了在感染和转染细胞中产生的第四类多重剪接的人类免疫缺陷病毒mRNA。tev在病毒生命周期中的调控方式与其他调控蛋白tat、rev和nef相似,并且在功能测定中显示出tat和rev活性。由于tev包含tat和rev的重要功能域,并且在转染后很早就产生,它可能是病毒表达初始阶段的重要调节因子。另一种包含env和rev序列的与rev相关的蛋白p18(6)Drev被鉴定出来,发现其没有可检测到的rev活性。