Pam King Sams
Penn Medicine Researchers Receive Two Major NIH Grants for Studies of Genome Folding.
Popular accounts of the human genome often depict it as a long string of DNA base pairs, but in reality the genome is separated into chromosomes that are tightly twisted and coiled into complex three-dimensional structures. These structures create a myriad of connections between sites on the genome that would be distant from one another if stretched out end-to-end. These “long range interactions” are not incidental — they regulate the activity of our genes during development and can cause disease when disrupted.
Now two teams of researchers at the Perelman School of Medicine at the University of Pennsylvania, each led by Jennifer E. Phillips-Cremins, Ph.D., an associate professor of Genetics at the Perelman School of Medicine and Bioengineering at the School of Engineering and Applied Science at the University of Pennsylvania, have been awarded grants totaling $9 million from the National Institutes of Health (NIH), as part of a major NIH Common Fund initiative to understand such 3D-genomic interactions.
The initiative, known as the 4D Nucleome Program, broadly aims to map higher-order genome structures across space and time, as well as to understand how the twists and loops of the DNA sequence govern genome function and cellular phenotype in health and disease.
Linking Genome Miswiring to Human Disease
Under one five-year grant, for a total of $3.1 million, a team of five principal investigators from Penn, including Drs. Rajan Jain, MD, an assistant professor of Cardiovascular Research and Cell & Developmental Biology, Eric Joyce, PhD, an assistant professor of Genetics, Melike Lakadamyali, PhD, an associate professor of Physiology, Golnaz Vahedi, PhD, an assistant professor of Genetics, and Phillips-Cremins will apply 3D architecture mapping and genome engineering tools to better understand a rare and often fatal inherited disorder called Friedrich’s Ataxia.
Friedrich’s Ataxia usually manifests in late childhood with difficulties in walking, talking, or controlling eye movements. Neurological signs and symptoms accumulate over time, with patients often requiring a wheelchair within a decade or two. The disorder also features progressive damage to the heart, which—depending on the severity of the condition—can cause an early death.
There is as yet no cure or disease-modifying treatment, although the ultimate cause of Friedrich’s Ataxia is well understood: It arises when both of the patient’s copies of a gene called FXN contain an abnormally high, or “expanded,” number of short DNA sequences called tandem repeats. The more repeats, the worse the disease. A major barrier in finding therapies for the disease is that researchers haven’t been able to determine how this abnormality within the gene leads to such a complex and devastating disorder.
The group will use single-cell techniques to investigate the possibility that the 3D folding patterns of the DNA are functionally linked to the severity of instability of a specific short tandem repeat sequence in FXN, leading to severe pathologic gene silence. Discoveries from the research funded by this grant will shed light on the causes—and possibly inspire new treatments—not only for Friedrich’s Ataxia but also of other repeat expansion disorders.
Unraveling Genomic Architecture’s Fourth Dimension
A second five-year grant, with total funding of $5.9 million over five years, will assemble a team of five principal investigators at Penn, including Drs. Gerd Blobel, MD, PhD, a professor of Pediatrics, Eric Joyce, PhD, an assistant professor of Genetics, Bomyi Lim, PhD, an assistant professor of Cell and Developmental Biology, Arjun Raj, PhD, professor of Genetics, and Phillips-Cremins, as well as Dr. Stanley Qi, of Stanford University. Raj and Lim’s primary appointments are in Penn Engineering’s departments of Bioengineering and Chemical and Biomolecular Engineering, respectively.
This project will examine the “fourth dimension” of genomic architecture, namely, how it changes over time. The team’s studies will employ model systems ranging from induced pluripotent stem cell reprogramming, to erythroid differentiation, and neural circuit activation.
The team plans to develop new microscopy and sequencing methods to capture a series of what are effectively snapshots of the 3D genome as it changes its conformations. These changes, which form and un-form DNA loops, occur across a broad range of time scales from seconds to minutes to weeks. The investigators will also explore the genome’s structure-function relationship by developing new strategies to engineer loops on demand and across time scales, then engineering and imaging loops in single cells to quantify their dynamics in more realistic contexts.
New Spatial Epigenetics Center of Excellence at Penn
The two new grants will catalyze the formation of the Spatial Epigenetics Center of Excellence (SECOE) at Penn, formally establishing a hub of internationally renowned investigators focused on spatial approaches for studying epigenetic and genetic regulation across a wide range of organ and disease systems, as well as a time scales ranging from milliseconds to decades. Led by Phillips-Cremins, the members of the SECOE will pioneer new imaging, genome engineering, sequencing and computational technologies to understand human development and disease through the lens of spatial connections.
"Over the last decade, methods advancing our ability to query DNA's higher-order folding patterns in the 3D nucleus have provided tremendous insight into how the genetic material works through long-range mechanisms to control genome function. Our center aims to establish a technology hub in Philadelphia to broaden the impact and application of spatial approaches to solve a wide range of fundamental biological questions." says Phillips-Cremins.
TOPIC: Basic Science
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 $8.6 billion enterprise.
Photo Caption: (Left to right) Top row: Jennifer E. Phillips-Cremins, Ph.D., an associate professor of Genetics at the Perelman School of Medicine and Bioengineering at the School of Engineering and Applied Science at the University of Pennsylvania, Rajan Jain, MD, an assistant professor of Cardiovascular Research and Cell & Developmental Biology, and Eric Joyce, PhD, an assistant professor of Genetics. Middle row: Melike Lakadamyali, PhD, an associate professor of Physiology, Golnaz Vahedi, PhD, an assistant professor of Genetics, and Gerd Blobel, MD, PhD, a professor of Pediatrics. Bottom row: Bomyi Lim, PhD, an assistant professor of Cell and Developmental Biology, Arjun Raj, PhD, professor of Genetics, and Stanley Qi, of Stanford University.