team of Michigan State University algae researchers have discovered a cellular “snooze button” that has the potential to improve biofuel production and offer insight into the early stages of cancer. The discovery that the protein CHT7 is a likely repressor of cellular quiescence, or resting state, is published in the current issue of the Proceedings of the National Academy of Sciences. This cellular switch, which influences algae’s growth and oil production, also controls cellular growth – and tumor growth – in humans.
Christoph Benning, MSU professor of biochemistry and molecular biology, and his colleagues, unearthed the protein’s potential while looking for ways to improve algae’s capacity as a biofuel. Its application in cancer research was a surprise finding that is now leading Benning’s lab in a new direction.
“Algae provide us with model organisms that rival, or possibly exceed, traditional yeast models,” Benning said. “It’s quite difficult to grow many types of human cells in test tubes. However, we can readily grow, manipulate and study algae, which have the genomic repertoire that make them relevant in their capacity to drive advances in human medicine.”
The discovery was made while tackling the conundrum of algae’s vexing inverse relationship with growing mass versus producing oil. When algae are awake, they grow; when they’re asleep, they produce oil.
“Producing oil is part of the cells’ survival strategy when it’s under stress,” said Chia-Hong Tsai, doctoral candidate with MSU’s Department of Energy Plant Research Laboratory and Department of Plant Biology and co-author. “They go into quiescence to conserve energy and nutrients. That’s when they produce the equivalent of vegetable oil. But to convert them into truly viable biofuel producers, we need them to grow and produce oil simultaneously.”
The secret for making this happen was CHT7 – the gatekeeper that cues cells to wake up or fall asleep. By engineering this protein, Benning’s team might one day develop an organism that can’t figure out how to doze and is always active.
This discovery gives scientists a promising new model to study tumor suppression and growth. “For cancer research, it’s a new paradigm,” Benning said. “The switch that tells an organism to grow, or possibly, go rogue and grow uncontrollably – that’s exactly what we want to understand. That is the first step of tumor growth.”
Because quiescent cells are found in many plants and animals, it’s a model that can provide important insights into the regulation of cellular behavior in organisms, such as us humans, in ways that traditional yeast models simply can’t replicate.
Additional MSU team members on this project included Jaruswan Warakanont, plant biology doctoral student; Tomomi Takeuchi, biochemistry and molecular biology doctoral student; Barbara Sears, professor emeritus of genetics and plant biology; and Eric Moellering, former doctoral candidate of biochemistry and molecular biology, now at Synthetic Genomics Inc.