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Nuclear organization and the control of HIV-1 transcription
被引:40
作者:
Marcello, A
Lusic, M
Pegoraro, G
Pellegrini, V
Beltram, F
Giacca, M
机构:
[1] Int Ctr Genet Engn & Biotechnol, Mol Med Lab, I-34012 Trieste, Italy
[2] INFM, NEST, I-56126 Pisa, Italy
[3] Scoula Normale Super, I-56126 Pisa, Italy
来源:
关键词:
HIV-1;
transcription;
tat transactivator;
LTR;
cyclin T1;
FRET;
PML;
speckles;
nuleus;
D O I:
10.1016/j.gene.2003.10.018
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
The regulation of transcription of the human immunodeficiency virus (HIV) is a complex event of significant pathological relevance, which recapitulates general concepts of cellular transcription with some peculiarities. The viral promoter is embedded in a chromatin structure that exerts powerful repression on transcription; activation of gene expression relies on the combined activity of a series of cellular factors that respond to different external stimuli, and on the function of a single viral regulatory protein, the Tat transactivator. Transcriptional activation is consequent to both chromatin remodeling and to the recruitment of elongation-competent RNA polymerase 11 complexes onto the integrated promoter, two events that require the coordinate, but transient, assembly of different protein complexes. Application of optical imaging techniques now allows us to appreciate the spatial and temporal evolvement of these reactions in vivo. The picture that is emerging is not only descriptive, but also relevant to the understanding of the regulation of the process. In particular, it appears that the confinement of biomolecules within specific subcellular compartments represents a way to control and coordinate the assembly of functional complexes that regulate viral gene expression. (C) 2003 Elsevier B.V. All rights reserved.
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页码:1 / 11
页数:11
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