Live-cell imaging reveals enhancer-dependent Sox2 transcription in the absence of enhancer proximity

Author:

Alexander Jeffrey M1ORCID,Guan Juan2,Li Bingkun3,Maliskova Lenka3,Song Michael34,Shen Yin345,Huang Bo267ORCID,Lomvardas Stavros89ORCID,Weiner Orion D16ORCID

Affiliation:

1. Cardiovascular Research Institute, University of California, San Francisco, San Francisco, United States

2. Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, United States

3. Institute for Human Genetics, University of California, San Francisco, San Francisco, United States

4. Pharmaceutical Sciences and Pharmacogenomics Graduate Program, University of California, San Francisco, San Francisco, United States

5. Department of Neurology, University of California, San Francisco, San Francisco, United States

6. Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, United States

7. Chan Zuckerberg Biohub, San Francisco, United States

8. Department of Biochemistry and Molecular Biophysics, Columbia University, New York City, United States

9. Mortimer B Zuckerman Mind Brain and Behavior Institute, Columbia University, New York City, United States

Abstract

Enhancers are important regulatory elements that can control gene activity across vast genetic distances. However, the underlying nature of this regulation remains obscured because it has been difficult to observe in living cells. Here, we visualize the spatial organization and transcriptional output of the key pluripotency regulator Sox2 and its essential enhancer Sox2 Control Region (SCR) in living embryonic stem cells (ESCs). We find that Sox2 and SCR show no evidence of enhanced spatial proximity and that spatial dynamics of this pair is limited over tens of minutes. Sox2 transcription occurs in short, intermittent bursts in ESCs and, intriguingly, we find this activity demonstrates no association with enhancer proximity, suggesting that direct enhancer-promoter contacts do not drive contemporaneous Sox2 transcription. Our study establishes a framework for interrogation of enhancer function in living cells and supports an unexpected mechanism for enhancer control of Sox2 expression that uncouples transcription from enhancer proximity.

Funder

American Heart Association

National Institute of General Medical Sciences

National Institute on Deafness and Other Communication Disorders

National Institute of Biomedical Imaging and Bioengineering

W. M. Keck Foundation

National Human Genome Research Institute

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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