共 35 条
Preventing gene silencing with human replicators
被引:34
作者:

Fu, HQ
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h-index: 0
机构: NCI, Mol Pharmacol Lab, Bethesda, MD 20892 USA

Wang, LX
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h-index: 0
机构: NCI, Mol Pharmacol Lab, Bethesda, MD 20892 USA

Lin, CM
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h-index: 0
机构: NCI, Mol Pharmacol Lab, Bethesda, MD 20892 USA

Singhania, S
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h-index: 0
机构: NCI, Mol Pharmacol Lab, Bethesda, MD 20892 USA

Bouhassira, EE
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h-index: 0
机构: NCI, Mol Pharmacol Lab, Bethesda, MD 20892 USA

Aladjem, MI
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h-index: 0
机构:
NCI, Mol Pharmacol Lab, Bethesda, MD 20892 USA NCI, Mol Pharmacol Lab, Bethesda, MD 20892 USA
机构:
[1] NCI, Mol Pharmacol Lab, Bethesda, MD 20892 USA
[2] Yeshiva Univ Albert Einstein Coll Med, Bronx, NY 10461 USA
关键词:
D O I:
10.1038/nbt1202
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Transcriptional silencing, one of the major impediments to gene therapy in humans, is often accompanied by replication during late S-phase. We report that transcriptional silencing and late replication were prevented by DNA sequences that can initiate DNA replication (replicators). When replicators were included in silencing-prone transgenes, they did not undergo transcriptional silencing, replicated early and maintained histone acetylation patterns characteristic of euchromatin. A mutant replicator, which could not initiate replication, could not prevent gene silencing and replicated late when included in identical transgenes and inserted at identical locations. These observations suggest that replicators introduce epigenetic chromatin changes that facilitate initiation of DNA replication and affect gene silencing. Inclusion of functional replicators in gene therapy vectors may provide a tool for stabilizing gene expression patterns.
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页码:572 / 576
页数:5
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