From silencing to gene expression: Real-time analysis in single cells

被引:556
作者
Janicki, SM
Tsukamoto, T
Salghetti, SE
Tansey, WP
Sachidanandam, R
Prasanth, KV
Ried, T
Shav-Tal, Y
Bertrand, E
Singer, RH
Spector, DL
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[2] Utsunomiya Univ, Utsunomiya, Tochigi 321, Japan
[3] NCI, Genet Branch, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[4] Albert Einstein Coll Med, Dept Anat & Struct Biol, Bronx, NY 10461 USA
[5] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10461 USA
[6] CNRS, Inst Genet Mol Montpellier, F-34293 Montpellier, France
关键词
D O I
10.1016/S0092-8674(04)00171-0
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
We have developed an inducible system to visualize gene expression at the levels of DNA, RNA and protein in living cells. The system is composed of a 200 copy transgene array integrated into a euchromatic region of chromosome 1 in human U20S cells. The condensed array is heterochromatic as it is associated with HP1, histone H3 methylated at lysine 9, and several histone methyltransferases. Upon transcriptional induction, HP1alpha is depleted from the locus and the histone variant H3.3 is deposited suggesting that histone exchange is a mechanism through which heterochromatin is transformed into a transcriptionally active state. RNA levels at the transcription site increase immediately after the induction of transcription and the rate of synthesis slows over time. Using this system, we are able to correlate changes in chromatin structure with the progression of transcriptional activation allowing us to obtain a real-time integrative view of gene expression.
引用
收藏
页码:683 / 698
页数:16
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