Tan W, Schwartz S
Microbiology and Tumorbiology Center, Karolinska Institute, Stockholm, Sweden.
J Virol. 1995 May;69(5):2932-45. doi: 10.1128/JVI.69.5.2932-2945.1995.
We have identified a sequence in the late 3' untranslated region of human papillomavirus type 1 mRNAs that acts posttranscriptionally to repress gene expression. Deletion analysis localized the inhibitory element to an AU-rich sequence between nucleotides 6958 and 6984 on the human papillomavirus type 1 genome. This sequence inhibits gene expression in an orientation-dependent manner. Upon transfection of eucaryotic cells with plasmids containing this sequence, approximately 4-fold-lower cytoplasmic mRNA levels and 64- to 128-fold-lower protein levels were produced compared with those produced by plasmids lacking the inhibitory sequence. Interestingly, providing the constitutive transport element of simian retrovirus type 1 in sense orientation counteracted inhibition exerted by the human papillomavirus type 1 sequence. Inhibition could also be overcome by the presence of human immunodeficiency virus type 1 Rev protein in trans and its target sequence, the Rev-responsive element, in cis. Rev is a nuclear protein and acts by promoting nuclear export of human immunodeficiency virus type 1 mRNAs encoding structural proteins. Our results are consistent with a model for human papillomavirus type 1 late-gene expression in which mRNAs containing human papillomavirus type 1 inhibitory sequences enter a nonproductive route in the nucleus, resulting in inefficient mRNA utilization. Rev directs mRNA containing inhibitory sequences to a productive route by interacting with the Rev-responsive element.
我们在人乳头瘤病毒1型mRNA的3'非翻译区晚期鉴定出一个序列,该序列在转录后发挥作用以抑制基因表达。缺失分析将抑制元件定位到人乳头瘤病毒1型基因组上核苷酸6958至6984之间的富含AU的序列。该序列以方向依赖的方式抑制基因表达。用含有该序列的质粒转染真核细胞后,与缺乏抑制序列的质粒相比,产生的细胞质mRNA水平降低约4倍,蛋白质水平降低64至128倍。有趣的是,以正义方向提供猿猴逆转录病毒1型的组成型转运元件可抵消人乳头瘤病毒1型序列施加的抑制作用。通过反式存在人免疫缺陷病毒1型Rev蛋白及其顺式作用的靶序列Rev反应元件也可以克服抑制作用。Rev是一种核蛋白,通过促进编码结构蛋白的人免疫缺陷病毒1型mRNA的核输出发挥作用。我们的结果与一种人乳头瘤病毒1型晚期基因表达模型一致,在该模型中,含有人类乳头瘤病毒1型抑制序列的mRNA在细胞核中进入非生产性途径,导致mRNA利用效率低下。Rev通过与Rev反应元件相互作用,将含有抑制序列的mRNA引导至生产性途径。