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Penn study brings new understanding to how fundamental DNA sequences govern gene activity

'Enhancer' sequences are drivers of many types of diseases, including cancer

University of Pennsylvania School of Medicine

PHILADELPHIA - A team of researchers from the Perelman School of Medicine at the University of Pennsylvania have shed new light on how the structure of regulatory sequences in DNA is packaged in a cell. "This work has implications for better understanding the role that gene sequences called enhancers play within our DNA for governing gene activity," said senior author Ken Zaret, PhD, a professor of Cell and Developmental Biology and director of the Institute for Regenerative Medicine. The findings are published this week in Molecular Cell.

Enhancers influence which genes are "on" or "off" in each type of cell and also control how much each the gene is activated. This level of control ultimately dictates the quantity of an encoded protein that is made in response to particular physiological conditions.

"Recent studies have shown that errors in enhancer function are crucial in various diseases, including many types of cancers," Zaret said. "Because of this, we need to detail how enhancers work."

Nucleosomes, the protein complexes around which DNA in every cell winds, inherently inhibit the binding of gene regulatory proteins to chromosomes. This packaging helps keep genes in the "off" position when needed. Most researchers have worked on the assumption that nucleosomes are absent at active enhancer sites along the genome, and therefore would not play a role in enhancer function.

However, when first author Makiko Iwafuchi-Doi, PhD, a postdoctoral fellow in the Zaret lab, modified the nucleosome mapping technique, she demonstrated that nucleosomes are present, at least in part, at enhancer sites, when gene regulatory proteins called pioneer factors are attached to them. This information provides a new view of how enhancer sequences and nucleosomes interact.

To elicit the necessary physiological programming or reprogramming in a cell, gene regulatory factors must be able to engage genes that are "off" and not regularly meant for expression in cells, a finding that the Zaret lab established in a 2015 Cell paper. These silenced genes are typically embedded in tightly coiled, "closed" areas covered by nucleosomes. Transcription factors with the highest reprogramming activity have the necessary capability to interact with target sites on closed nucleosome DNA. These transcription proteins are the pioneer factors and named such because they initiate molecular changes in closed chromatin.

The team on the Molecular Cell paper went on to show that pioneer factors help expose stretches of DNA on individual nucleosomes to which they are bound. By kicking out a repressive protein called a linker histone, the pioneer factors allow other regulatory factors to gain access to the DNA. This, in turn, allows enhancers to activate genes and promote normal cell functions.

Together, these studies reveal novel insights into the ways that pioneer factors initiate and maintain enhancer sites in an active, or "on," state. The pioneer factors play important roles in controlling how different cells develop in an embryo. They also play a role in allowing genes to be responsive to hormones, including hormone-responsive human breast and prostate cancers.

"We anticipate that by understanding the basic mechanisms by which pioneer factors control enhancer function, we will be able to enhance the process by which we can change one type of cell into another," Zaret said. "This will be helpful in generating new models of human disease and, in the future, new cells for therapeutics."


This research was supported by National Institutes of Health grants (R37GM36477, P01DK049210, HG004160).

Penn Medicine is one of the world's leading academic medical centers, dedicated to the related missions of medical education, biomedical research, and excellence in patient care. Penn Medicine consists of the Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania (founded in 1765 as the nation's first medical school) and the University of Pennsylvania Health System, which together form a $5.3 billion enterprise.

The Perelman School of Medicine has been ranked among the top five medical schools in the United States for the past 18 years, according to U.S. News & World Report's survey of research-oriented medical schools. The School is consistently among the nation's top recipients of funding from the National Institutes of Health, with $373 million awarded in the 2015 fiscal year.

The University of Pennsylvania Health System's patient care facilities include: The Hospital of the University of Pennsylvania and Penn Presbyterian Medical Center -- which are recognized as one of the nation's top "Honor Roll" hospitals by U.S. News & World Report -- Chester County Hospital; Lancaster General Health; Penn Wissahickon Hospice; and Pennsylvania Hospital -- the nation's first hospital, founded in 1751. Additional affiliated inpatient care facilities and services throughout the Philadelphia region include Chestnut Hill Hospital and Good Shepherd Penn Partners, a partnership between Good Shepherd Rehabilitation Network and Penn Medicine.

Penn Medicine is committed to improving lives and health through a variety of community-based programs and activities. In fiscal year 2015, Penn Medicine provided $253.3 million to benefit our community.

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