Source: Salk Institute for Biological Studies
Salk scientists discover new protein complex that keeps embryonic stem cells at stage of fullest potential, a key to regenerative medicine
Embryonic stem cells (ESCs) are the very definition of being full of potential, given that they can become any type of cell in the body. Once they start down any particular path toward a type of tissue, they lose their unlimited potential. Scientists have been trying to understand why and how this happens in order to create regenerative therapies that can, for example, coax a person’s own cells to replace damaged or diseased organs.
Scientists from the Salk Institute discovered a new protein complex that keeps the brakes on stem cells, allowing them to maintain their indefinite potential. The new complex, called GBAF and detailed in Nature Communications on December 3, 2018, could provide a future target for regenerative medicine.
“This project started as an exploration of embryonic stem cell pluripotency, which is this property that allows ESCs to become all different cell types in the body,” says Diana Hargreaves, an assistant professor in Salk’s Molecular and Cell Biology Laboratory and the senior author of the paper. “It’s very important to know how various networks of genes control pluripotency, so finding a previously unknown protein complex that plays such an important regulatory role was very exciting.”
Hargreaves’s team wanted to better understand how these subunits come together and how particular subunits might dictate a complex’s function. So they turned to a protein called BRD9, which was known to associate with the BAF family of chromatin remodelers and was suspected to be a subunit. The team applied a chemical inhibitor of BRD9 to dishes of embryonic stem cells and performed a series of experiments to comprehensively analyze the cells’ pluripotency in association with changes in BAF complex activity.
The group was surprised to discover that BRD9 acts as a brake on embryonic stem cell development. When BRD9 is working, cells retain their pluripotency, whereas when its activity is inhibited cells start moving on to the next stage of development. Further work to identify which BAF complexes were at work in the cells revealed another surprise: BRD9 was part of an as-yet-unknown BAF complex.
“For me, what was most exciting about our study was the fact that we had discovered a new BAF complex in embryonic stem cells,” says Jovylyn Gatchalian, a Salk research associate and the paper’s first author.
Adds Hargreaves, “What we see with this work is that there’s biochemical diversity at the level of individual variants of the BAF complex that allows for greater regulatory control. Understanding the complexities of that control is going to be key to any regenerative therapies.”
The team next wants to examine how GBAF interacts with various structural proteins that help keep the genome organized.
Other authors included Shivani Malik, Josephine Ho, Dong-Sung Lee, Timothy W. R. Kelso, Maxim N. Shokhirev and Jesse R. Dixon of Salk.
The work was funded by the National Institutes of Health (R00 CA184043-03), the V Foundation for Cancer Research (V2016-006), a T32 Cancer Training Grant (T32CA009370) and a National Institute of General Medical Sciences National Research Service Award (F32 GM128377-01).
About the Salk Institute for Biological Studies:
Every cure has a starting point. The Salk Institute embodies Jonas Salk’s mission to dare to make dreams into reality. Its internationally renowned and award-winning scientists explore the very foundations of life, seeking new understandings in neuroscience, genetics, immunology, plant biology and more. The Institute is an independent nonprofit organization and architectural landmark: small by choice, intimate by nature and fearless in the face of any challenge. Be it cancer or Alzheimer’s, aging or diabetes, Salk is where cures begin.
Barbara Jacoby is an award winning blogger that has contributed her writings to multiple online publications that have touched readers worldwide.