Imaging transcription dynamics at endogenous genes in living Drosophila tissues

被引:23
作者
Yao, Jie [2 ]
Zobeck, Katie L. [1 ]
Lis, John T. [1 ]
Webb, Watt W. [2 ]
机构
[1] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
[2] Cornell Univ, Sch Appl & Engn Phys, Ithaca, NY 14853 USA
关键词
transcription; genes; polytene; chromosomes; chromatin; multiphoton microscopy; DNA; genome; crosslinking; immunostaining;
D O I
10.1016/j.ymeth.2008.06.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
How transcription of individual genes is regulated in a single, intact, three-dimensionally organized cell nucleus remains mysterious. Recently, live cell imaging has become an essential tool to dissect the in vivo mechanisms of gene transcription. it not only examines functions of transcription factors at their gene targets within the chromatin context, but it also provides a non-disruptive approach for observing the dynamics of a transcription cycle in real time. However, the identification of any endogenous gene loci and their associated transcription factors remains technically difficult. Here, we describe the method of imaging the transcriptional dynamics of heat shock genes in Drosophila polytene chromosomes in living salivary gland tissues by multiphoton microscopy (MPM). This method has provided the experimental capability to visualize the assembly and dynamics of individual transcription factors and regulators and to dissect their functions at their endogenous gene targets in living cells. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:233 / 241
页数:9
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