POLYMERASE CHAIN-REACTION INSITU - INTRACELLULAR AMPLIFICATION AND DETECTION OF HIV-1 PROVIRAL DNA AND OTHER SPECIFIC GENES

被引:57
作者
BAGASRA, O
SESHAMMA, T
POMERANTZ, RJ
机构
[1] Section of Molecular Retrovirology, Infectious Disease Division, Department of Medicine, Philadelphia, PA 19107, Jefferson Medical College Thomas Jefferson University Jefferson Alumni Hall
关键词
INSITU; POLYMERASE CHAIN REACTION; PATHOGENESIS; LATENCY; TUMOR LOAD; VIRAL LOAD; HIV-1;
D O I
10.1016/0022-1759(93)90265-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The ability to detect a single copy of a specific gene in situ has many advantages and multiple applications in molecular biology, pathology and cell biology. We report here a unique, highly sensitive and specific technique which can be utilized to detect a single copy of human immunodeficiency virus type I (HIV-1) provirus and other genes, at the single cell level, by in situ amplification of a portion of a gene sequence. In this method, a polymerase chain reaction (PCR) can be carried out in situ, in fixed cells, on specially designed glass slides. After amplification one can detect the amplified signals by the in situ hybridization method, utilizing either biotinylated probes or P-32-labelled probes. The early molecular events in the retroviral life-cycle of HIV-1, in specific target cells, are demonstrated utilizing in situ PCR. The techniques utilized in this procedure and various potential uses of this methodology are described.
引用
收藏
页码:131 / 145
页数:15
相关论文
共 48 条
[21]  
IKEYCHI K, 1990, J VIROL, V64, P4426
[22]   A SENSITIVE NONISOTOPIC HYBRIDIZATION ASSAY FOR HIV-1 DNA [J].
KELLER, GH ;
HUANG, DP ;
MANAK, MM .
ANALYTICAL BIOCHEMISTRY, 1989, 177 (01) :27-32
[23]   TEMPORAL ASPECTS OF DNA AND RNA-SYNTHESIS DURING HUMAN IMMUNODEFICIENCY VIRUS-INFECTION - EVIDENCE FOR DIFFERENTIAL GENE-EXPRESSION [J].
KIM, SY ;
BYRN, R ;
GROOPMAN, J ;
BALTIMORE, D .
JOURNAL OF VIROLOGY, 1989, 63 (09) :3708-3713
[24]  
Komminoth P, 1992, Diagn Mol Pathol, V1, P85, DOI 10.1097/00019606-199206000-00001
[25]  
KUOPING C, 1992, HISTOCHEM CYTOCHEM, V40, P333
[26]  
KWOK S, 1989, PCR PROTOCOLS GUIDE, P142
[27]   CONFOCAL MICROSCOPIC DETECTION OF HUMAN-IMMUNODEFICIENCY-VIRUS RNA-PRODUCING CELLS [J].
LEWIS, DE ;
MINSHALL, M ;
WRAY, NP ;
PADDOCK, SW ;
SMITH, LC ;
CRANE, MM .
JOURNAL OF INFECTIOUS DISEASES, 1990, 162 (06) :1373-1378
[28]   VIRAL-DNA CARRIED BY HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 VIRIONS [J].
LORI, F ;
VERONESE, FD ;
DEVICO, AL ;
LUSSO, P ;
REITZ, MS ;
GALLO, RC .
JOURNAL OF VIROLOGY, 1992, 66 (08) :5067-5074
[29]   ADAPTATION OF LYMPHADENOPATHY ASSOCIATED VIRUS (LAV) TO REPLICATION IN EBV-TRANSFORMED B-LYMPHOBLASTOID CELL-LINES [J].
MONTAGNIER, L ;
GRUEST, J ;
CHAMARET, S ;
DAUGUET, C ;
AXLER, C ;
GUETARD, D ;
NUGEYRE, MT ;
BARRESINOUSSI, F ;
CHERMANN, JC ;
BRUNET, JB ;
KLATZMANN, D ;
GLUCKMAN, JC .
SCIENCE, 1984, 225 (4657) :63-66
[30]   INVIVO FOOTPRINTING OF A MUSCLE SPECIFIC ENHANCER BY LIGATION MEDIATED PCR [J].
MUELLER, PR ;
WOLD, B .
SCIENCE, 1989, 246 (4931) :780-786