HIV-1 integration sites are flanked by potential MARs that alone can act as promoters

被引:21
作者
Kulkarni, A [1 ]
Pavithra, L [1 ]
Rampalli, S [1 ]
Mogare, D [1 ]
Babu, K [1 ]
Shiekh, G [1 ]
Ghosh, S [1 ]
Chattopadhyay, S [1 ]
机构
[1] Natl Ctr Cell Sci, Pune 411007, Maharashtra, India
关键词
HIV-1; integration; matrix associated regions; IgH MAR; p53; promoter; human genome analysis;
D O I
10.1016/j.bbrc.2004.07.170
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Matrix attachment regions (MARs) are cis regulatory elements that modulate gene expression in a tissue and cell stage specific manner. Recent reports show that viral integration within the genome takes place at nonrandom active genes. We have checked for the presence of MARs in the vicinity of the reported 524 HIV-1 integration sites. Our studies show that in 92.5% cases, MARs flank the integration sites. Similarly, for adeno-associated virus, two potential MARs were present next to the integration site on the human chromosome. Earlier we have shown that short MAR sequences present upstream of HIV-1 LTR promote processive transcription at a distance. Here, using a well-studied IgH-MAR and another potential MAR from p53 promoter, we demonstrate that MARs alone can act as promoters. Thus, we propose that MAR elements near the HIV-1 integration sites can act as potential promoters, which may facilitate proviral integration and transcription. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:672 / 677
页数:6
相关论文
共 27 条
[1]   PROTEIN - DNA INTERACTIONS AT CHROMOSOMAL LOOP ATTACHMENT SITES [J].
BLASQUEZ, VC ;
SPERRY, AO ;
COCKERILL, PN ;
GARRARD, WT .
GENOME, 1989, 31 (02) :503-509
[2]  
BODE J, 1998, GENE THER MOL BIOL, V1, P551
[3]   TETHERING HUMAN-IMMUNODEFICIENCY-VIRUS-1 INTEGRASE TO A DNA SITE DIRECTS INTEGRATION TO NEARBY SEQUENCES [J].
BUSHMAN, FD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (20) :9233-9237
[4]  
Chou KS, 1996, INT J CANCER, V65, P20, DOI 10.1002/(SICI)1097-0215(19960103)65:1<20::AID-IJC4>3.0.CO
[5]  
2-3
[6]   CHROMOSOMAL LOOP ANCHORAGE OF THE KAPPA IMMUNOGLOBULIN GENE OCCURS NEXT TO THE ENHANCER IN A REGION CONTAINING TOPOISOMERASE-II SITES [J].
COCKERILL, PN ;
GARRARD, WT .
CELL, 1986, 44 (02) :273-282
[7]   Matrix attachment region-dependent function of the immunoglobulin μ enhancer involves histone acetylation at a distance without changes in enhancer occupancy [J].
Fernández, LA ;
Winkler, M ;
Grosschedl, R .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (01) :196-208
[8]   Nuclear matrix attachment regions confer long-range function upon the immunoglobulin μ enhancer [J].
Fernández, LA ;
Winkler, N ;
Forrester, W ;
Jenuwein, T ;
Grosschedl, R .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1998, 63 :515-524
[9]   Nuclear matrix attachment regions antagonize methylation-dependent repression of long-range enhancer-promoter interactions [J].
Forrester, WC ;
Fernández, LA ;
Grosschedl, R .
GENES & DEVELOPMENT, 1999, 13 (22) :3003-3014
[10]   Resting CD4+ T cells from human immunodeficiency virus type I (HIV-1)-infected individuals carry integrated HIV-1 Genomes within actively transcribed host genes [J].
Han, YF ;
Lassen, K ;
Monie, D ;
Sedaghat, AR ;
Shimoji, S ;
Liu, X ;
Pierson, TC ;
Margolick, JB ;
Siliciano, RF ;
Siliciano, JD .
JOURNAL OF VIROLOGY, 2004, 78 (12) :6122-6133