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Showing posts with label Systems Biology. Show all posts
Showing posts with label Systems Biology. Show all posts

Friday, September 2, 2011

Glowing, Blinking Bacteria Reveal How Cells Synchronize Biological Clocks


Biologists have long known that organisms from bacteria to humans use the 24 hour cycle of light and darkness to set their biological clocks. But exactly how these clocks are synchronized at the molecular level to perform the interactions within a population of cells that depend on the precise timing of circadian rhythms is less well understood.
Green fluorescent protein causes the E. coli to glow 
when the cells' clock is activated. (Credit: UC San Diego)

To better understand that process, biologists and bioengineers at UC San Diego created a model biological system consisting of glowing, blinking E. coli bacteria. This simple circadian system, the researchers report in the September 2 issue of Science, allowed them to study in detail how a population of cells synchronizes their biological clocks and enabled the researchers for the first time to describe this process mathematically.

"The cells in our bodies are entrained, or synchronized, by light and would drift out of phase if not for sunlight," said Jeff Hasty, a professor of biology and bioengineering at UC San Diego who headed the research team. "But understanding the phenomenon of entrainment has been difficult because it's difficult to make measurements. The dynamics of the process involve many components and it's tricky to precisely characterize how it works. Synthetic biology provides an excellent tool for reducing the complexity of such systems in order to quantitatively understand them from the ground up. It's reductionism at its finest."

To study the process of entrainment at the genetic level, Hasty and his team of researchers at UC San Diego's Biocircuits Institute combined techniques from synthetic biology, microfluidic technology and computational modeling to build a microfluidic chip with a series of chambers containing populations of E. coli bacteria. Within each bacterium, the genetic machinery responsible for the biological clock oscillations was tied to green fluorescent protein, which caused the bacteria to periodically fluoresce.



To simulate day and night cycles, the researchers modified the bacteria to glow and blink whenever arabinose -- a chemical that triggered the oscillatory clock mechanisms of the bacteria -- was flushed through the microfluidic chip. In this way, the scientists were able to simulate periodic day-night cycles over a period of only minutes instead of days to better understand how a population of cells synchronizes its biological clocks.

Hasty said a similar microfluidic system in principal could be constructed with mammalian cells to study how human cells synchronize with light and darkness. Such genetic model systems would have important future applications since scientists have discovered that problems with the biological clock can result in many common medical problems from diabetes to sleep disorders.

Other members of Hasty's team included Lev Tsimring, associate director of the BioCircuits Institute, and bioengineering graduate students Octavio Mondragon, Tal Danino and Jangir Selimkhanov. Their research was supported by grants from the National Institutes of Health and General Medicine and the San Diego Center for Systems Biology.

Story Source: The above story is reprinted (with editorial adaptations) from materials provided by University of California - San Diego.

Saturday, July 3, 2010

Scientists Find Direct Line from Development to Growth


It may seem intuitive that growth and development somehow go together so that plants and animals end up with the right number of cells in all the right places. But it is only now that scientists at the Duke Institute for Genome Sciences & Policy have gotten some of the first insights into how this critical coordination actually works in a plant.
Arabidopsis thaliana.
Arabidopsis thaliana. (Credit: iStockphoto)

The answer is surprisingly simple.

A well-known developmental protein called Short-root has been found to directly control the activity, in both time and space, of other well-known genes involved in cell division.

"It's a remarkably straightforward answer," said Philip Benfey, director of the IGSP's Center for Systems Biology. "Considering the level of complexity that is so often found in biology, this is simplicity itself."

The researchers report their findings on July 1 in the journal Nature.

Benfey's group and others have studied the molecular-level events that determine what particular cells in Arabidopsis plants will become in considerable detail. Those events involve genetic partners Short-root and Scarecrow along with a couple of microRNAs.

Researchers also have a pretty good understanding of the intrinsic factors that allow cells to go through their cycle and divide into two daughter cells. "What was missing was a connection between the two," said Rosangela Sozzani, a postdoctoral researcher in Benfey's lab and first author of the new study.

To shed light on that connection, Sozzani and her collaborators combined a number of experimental techniques and technologies to produce a dynamic, genome-wide view of the genetic events that Short-root and its partner Scarecrow set into motion within a single type of cell. At the very same time that cells divide, Short-root and Scarecrow switch on the gene cyclin D6, they report. Cyclin D6 is one of a family of genes that govern cell growth and division.

Benfey says the discovery in plants has immediate practical relevance given the central role of plants to human life, in the form of "food, feed, fuel and fiber." It's also likely that the "logic" behind plants' growth and development will carry over to other species, perhaps even our own. In fact, he and Sozzani note, animals including humans have cyclin D6 too.

"It's not just molecules," Benfey said. "There are evolutionary relationships. Once these fundamental processes got worked out, they are likely to have been kept around."

Jim Murray from the University of Cardiff was a key collaborator on the study. The work was funded by grants from the National Institutes of Health and the National Science Foundation.