A team led by researchers at Baylor College of Medicine and the has uncovered a new piece of the puzzle of how gene expression is orchestrated. Published in the journal , the findings reveal a novel mechanism that coordinates the assembly of components inside cells that control gene expression. The mechanism not only is essential for normal cell function, but also has been implicated in cancer, neurodegeneration and HIV infection, and could suggest new ways to treat these conditions.
“Most previous studies have focused on particular cellular components that turn genes completely on or off,” said co-corresponding author , assistant professor of and the at Baylor. “Our work reveals a new perspective – that the proteins that regulate the rate of gene expression also can work collectively to finely tune expression levels in many different settings. We identified a mechanism that brings these proteins together and plays widespread roles in health and disease.”
In previous work with colleagues at KU Leuven in Belgium, the team had studied protein interactions in leukemia and HIV infection, specifically those mediated by protein regions called TFIIS N-terminal domains (TNDs). In the current study, the researchers extended the study of TNDs and found them in many other proteins.
“Everywhere we looked, we found these domains, in particular in the machinery that regulates transcription elongation, one of the first steps of gene expression in all human cells. Transcription elongation is a complex cellular process that involves many different proteins working together,” said first author , a postdoctoral fellow in the . “We discovered that TNDs are the most enriched structural element in all transcription elongation factors. Once you look for them, you find that all the important protein complexes involved in transcription elongation have a TND or bind a protein that has one.”
Previous work suggested to the researchers that TNDs act like a docking platform for other protein regions, specifically for small portions of unstructured proteins known as TND-interacting motifs (TIMs).
Proteins have segments with a well-organized 3-D structure, but many also have segments that lack such organization. These disordered or unstructured regions are often functional.
“One remarkable thing about these unstructured regions is their unusual behavior as molecules,” said co-corresponding author Dr. Vaclav Veverka, structural biologist and group leader at the (IOCB Prague). “Imagine a TIM as a string that is loose at one end and moves as if being blown around in a hurricane. But when it finds its TND partner, the string curls up and holds on very tightly to the TND to keep it close.” The researchers show this attachment plays an important role in the early stages of gene expression.
“We first determined that TNDs and TIMs bound together in ‘test tube’ type of experiments, but it was really exciting to see that they bind to each other in living cells, validating the relevance of our observations in living systems,” Cermakova said. “We also determined that the TND-TIM interactions are highly specific.”
“I was surprised to see that IWS1, a protein previously thought to be a secondary player in the transcription elongation machinery, acts as a central organizer of these factors,” said Hodges, a member of Baylor’s .
“We found that IWS1 uses specific TND-TIM interactions to coordinate the activities of many transcription regulators at the same time, making it appear like a conductor at a symphony that keeps all the factors working in harmony and close by,” Veverka said.
The team also explored the consequences of disrupting a single unstructured protein region on the harmony of the transcription elongation process.
“Hundreds of genes with important functions were altered when we disrupted even a single unstructured region,” Hodges said. “The first step of gene expression started, but was paused and unable to be completed, preventing efficient gene expression.”
The study highlights the underappreciated role of disordered protein interactions as key orchestrators in gene expression and other complex biological functions. The findings also can contribute to a better understanding of diseases such as cancer, viral infections, neurodevelopmental disorders and potentially other conditions in which these factors are disrupted. TNDs and TIMs may represent important novel targets for improved treatments for these conditions.
Other contributors to this work include Jonas Demeulemeester, Vanda Lux, Monika Nedomova, Seth R. Goldman, Eric A. Smith, Pavel Srb, Rozalie Hexnerova, Milan Fabry, Marcela Madlikova, Magdalena Horejsi, Jan De Rijck, Zeger Debyser and Karen Adelman. The authors are affiliated with one or more of the following institutions: Baylor College of Medicine, Czech Academy of Sciences, KU Leuven in Belgium, Harvard Medical School, The University of Texas MD Anderson Cancer Center, Rice University and Charles University at the Czech Republic.
For a complete list of financial support for this work, see the .
