Measurement of gene regulation in individual cells reveals rapid switching between promoter states

Author:

Sepúlveda Leonardo A.12,Xu Heng12,Zhang Jing12,Wang Mengyu123,Golding Ido1234

Affiliation:

1. Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX 77030, USA.

2. Center for Theoretical Biological Physics, Rice University, Houston, TX 77005, USA.

3. Graduate Program in Structural and Computational Biology and Molecular Biophysics, Baylor College of Medicine, Houston, TX 77030, USA.

4. Center for the Physics of Living Cells, University of Illinois at Urbana–Champaign, Urbana, IL 61801, USA.

Abstract

Stochastic properties of phage promoter Full understanding of regulated gene expression requires characterization of stochastic variation in the activity of individual promoters. To avoid cell-to-cell variability and variation between the activity of specific gene copies, Sepúlveda et al. investigated the behavior of the lysogeny maintenance promoter of phage lambda in individual Escherichia coli cells. They measured the concentration of transcription factor and the actual number of mRNAs produced, and used mathematical modeling to discern the stochastic activity of the regulated promoter. The promoter underwent switching between configurations that occurred more rapidly than the lifetime of mRNA molecules produced, and individual copies of the same gene functioned independently in the same cell. Such studies can reveal new aspects of systems that have been well studied by more conventional techniques. Science , this issue p. 1218

Funder

NIH

NSF

Welch Foundation

John S. Dunn Foundation

Burroughs Wellcome Fund Career Award at the Scientific Interface

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference47 articles.

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2. M. Ptashne A. Gann Genes and Signals (Cold Spring Harbor Laboratory Press Cold Spring Harbor NY 2002).

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4. DNA looping can enhance lysogenic CI transcription in phage lambda

5. Enhancer-like long-range transcriptional activation by   CI-mediated DNA looping

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