Laimins L A, Tsichlis P, Khoury G
Nucleic Acids Res. 1984 Aug 24;12(16):6427-42. doi: 10.1093/nar/12.16.6427.
The 3' terminal region of the Prague strain of Rous sarcoma virus (PrRSV) contains at least three distinct domains that comprise two functional enhancer elements. Two of these domains (designated B and C) are found in the U3 region of the 3' long terminal repeat (LTR) while the third (designated A) is located in the sequences immediately preceding the LTR termed XSR sequences. Combinations of adjacent domains [e.g., (A + B or B + C)] are capable of activating the expression of the SV40 early promoter (21 bp repeats and TATA box) coupled to coding sequences from the prokaryotic gene chloramphenicol acetyltransferase (CAT) while a single domain is inactive. Furthermore, duplication or triplication of the central domain B restores activity. The related, Schmidt-Ruppin, strain of RSV, contains an almost identical 3' LTR element, but differs in the enhancer sequences immediately preceding the 3' LTR. A model is presented in which the sequence differences may contribute to the difference in disease spectrum of transformation defective (td) variants of these viruses.
劳氏肉瘤病毒布拉格株(PrRSV)的3'末端区域包含至少三个不同的结构域,这些结构域构成了两个功能性增强子元件。其中两个结构域(命名为B和C)位于3'长末端重复序列(LTR)的U3区域,而第三个结构域(命名为A)位于紧接LTR之前的序列中,称为XSR序列。相邻结构域的组合[例如,(A + B或B + C)]能够激活与原核基因氯霉素乙酰转移酶(CAT)编码序列相连的SV40早期启动子(21 bp重复序列和TATA盒)的表达,而单个结构域则无活性。此外,中央结构域B的重复或三倍化可恢复活性。相关的劳斯肉瘤病毒施密特-鲁平株含有几乎相同的3' LTR元件,但在3' LTR之前的增强子序列有所不同。本文提出了一个模型,其中序列差异可能导致这些病毒的转化缺陷(td)变体在疾病谱上的差异。