Cells calculate ratios to control gene expression

Behavior of cells over time after they have received a Tgf-beta signal. The brightness of the nuclei (circled in red) indicates how much Smad protein is present. This brightness varies from cell to cell, but the ratio of brightness after the signal to before the signal is about the same. The ratio guides the cell to modify gene expression accordingly, suggesting that cells can monitor protein abundance over time, and perform simple division to decipher protein abundance into gene expression. Credit: Courtesy of the Goentoro lab

In multicellular animals, cells communicate by emitting and receiving proteins, a process called signaling. One of the most common signaling pathways is the transforming growth factor b (Tgf-b) pathway, which functions in all animal species throughout their lifetimes and regulates numerous biological processes, such as instructing cells how to differentiate—whether a stem cell will become a muscle cell or a bone cell, for example.


But how do cells decipher those signals and use that information to guide ? The answer, according to new research from the laboratory of Lea Goentoro, assistant professor of biology at Caltech: the cells perform simple division. In other words, they do math.

The findings, which appear in a paper in the April 4 issue of Proceedings of the National Academy of Sciences, contradict previous hypotheses about how cells interpret signals. The work was led by Christopher Frick, a graduate student in biochemistry and molecular biophysics.

“Malfunctions in the Tgf-b pathway have been implicated in many types of cancer, and that’s why it’s important for us to study how it works, to understand how cells use this pathway to take information from their environment and turn it into altered gene ,” Goentoro says. “We found that cells are able to monitor the abundance of a certain protein over time and somehow divide the abundance after the Tgf-b signal by the abundance before the signal. The cell then uses this ratio to adjust gene expression accordingly.”

The cell’s detection of the Tgf-b signal triggers a series of molecular interactions, culminating in changes in the abundance of a protein called Smad3. A kind of messenger, Smad3 is activated at the cell membrane when a cell encounters the Tgf-β signal, and ultimately ends up in the nucleus of the cell where it directs gene expression. Biologists have commonly believed that the degree to which gene expression is changed will depend on how much Smad protein is produced after exposure to Tgf-β.

In order to study how Smad responds to Tgf-b in real time, the researchers made movies of the process in . They discovered that the pathway did not behave as biologists had previously thought. After exposure to the Tgf-b signal, the…

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