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巨细胞病毒转化结构域III(mtrIII)的图谱绘制与DNA序列分析

Mapping and DNA sequence analysis of the cytomegalovirus transforming domain III (mtrIII).

作者信息

Wang J, Razzaque A

机构信息

Division of Viral Products, CBER, FDA, Bethesda, MD 20892.

出版信息

Virus Res. 1993 Dec;30(3):221-38. doi: 10.1016/0168-1702(93)90092-2.

Abstract

The transforming activity of XbaI fragment E (map units 0.685-0.770) of human cytomegalovirus Towne strain was originally localized in two terminal segments, 3 kb XbaI-BamHI EM (mtrII) and 7.5 kb BamHI-XbaI EJ (mtrIII). Three immediate-early genes, IE1 to IE3, are located in the same region (map unit 0.685-0.770), and IE1 is located in the EJ fragment. IE1 protein increases chromatin transcriptional activity and causes alteration in chromatin conformation. In this study, we have investigated the potential transforming activity of IE1, IE1 plus its promoter-regulatory region (IE P/R), and the remaining fragment of EJ after deletion of IE1 plus IE P/R. Our results clearly demonstrate that IE1 or IE1 plus IE P/R is not involved in transformation, and that the transforming activity of mtrIII is located in a 2.1 kb SalI-XbaI subfragment of EJ. DNA sequence analysis reveals four putative open reading frames (ORFs) L1, L2, L3 and R1 in the 2.1 kb fragment. The data from the deletion clones of the 2.1 kb fragment and also by disruption of individual ORFs by restriction enzyme digestion, suggest that a complete ORF L3 or R1 may be essential but not sufficient for the transforming activity. Because significant reduction in transforming activity is obtained by interrupting ORFs LI and L2, these ORFs may be required for the full transforming activity.

摘要

人巨细胞病毒汤氏株XbaI片段E(图谱单位0.685 - 0.770)的转化活性最初定位于两个末端片段,即3 kb的XbaI - BamHI EM(mtrII)和7.5 kb的BamHI - XbaI EJ(mtrIII)。三个立即早期基因,即IE1至IE3,位于同一区域(图谱单位0.685 - 0.770),且IE1位于EJ片段中。IE1蛋白可增加染色质转录活性并导致染色质构象改变。在本研究中,我们研究了IE1、IE1及其启动子调控区域(IE P/R)以及缺失IE1加IE P/R后的EJ剩余片段的潜在转化活性。我们的结果清楚地表明,IE1或IE1加IE P/R不参与转化,且mtrIII的转化活性位于EJ的一个2.1 kb SalI - XbaI亚片段中。DNA序列分析揭示了该2.1 kb片段中有四个推定的开放阅读框(ORF)L1、L2、L3和R1。来自该2.1 kb片段缺失克隆的数据以及通过限制酶消化破坏单个ORF的数据表明,完整的ORF L3或R1可能对转化活性至关重要但并不充分。因为通过中断ORF L1和L2可使转化活性显著降低,所以这些ORF可能是完全转化活性所必需的。

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