Temperature variations could have driven the division of protocells

A simple mechanism could underlie the growth and self-replication of protocells-;putative ancestors of modern living cells-;suggests a study publishing September 3 in Biophysical Journal. Protocells are vesicles bounded by a membrane bilayer and are potentially similar to the first unicellular common ancestor (FUCA). On the basis of relatively simple mathematical principles, the proposed model suggests that the main force driving protocell growth and reproduction is the temperature difference that occurs between the inside and outside of the cylindrical protocell as a result of inner chemical activity.

The initial motivation of our study was to identify the main forces driving cell division. This is important because cancer is characterized by uncontrolled cell division. This is also important to understand the origin of life."

Romain Attal, Study Author, Universcience

The splitting of a cell to form two daughter cells requires the synchronization of numerous biochemical and mechanical processes involving cytoskeletal structures inside the cell. But in the history of life, such complex structures are a high-tech luxury and must have appeared much later than the ability to split. Protocells must have used a simple splitting mechanism to ensure their reproduction, before the appearance of genes, RNA, enzymes, and all the complex organelles present today, even in the most rudimentary forms of autonomous life.

In the new study, Attal proposed a model based on the idea that the early forms of life were simple vesicles containing a particular network of chemical reactions-;a precursor of modern cellular metabolism. The main hypothesis is that molecules composing the membrane bilayer are synthesized inside the protocell through globally exothermic, or energy-releasing, chemical reactions.

The slow increase of the inner temperature forces the hottest molecules to move from the inner leaflet to the outer leaflet of the bilayer. This asymmetric movement makes the outer leaflet grow faster than the inner leaflet. This differential growth increases the mean curvature and amplifies any local shrinking of the protocell until it splits in two. The cut occurs near the hottest zone, around the middle.

"The scenario described can be viewed as the ancestor of mitosis," Attal says. "Having no biological archives as old as 4 billion years, we don't know exactly what FUCA contained, but it was probably a vesicle bounded by a lipid bilayer encapsulating some exothermic chemical reactions."

Although purely theoretical, the model could be tested experimentally. For example, one could use fluorescent molecules to measure temperature variations inside eukaryotic cells, in which mitochondria are the main source of heat. These fluctuations could be correlated with the onset of mitosis and with the shape of the mitochondrial network.

If borne out by future investigations, the model would have several important implications, Attal says. "An important message is that the forces driving the development of life are fundamentally simple," he explains. "A second lesson is that temperature gradients matter in biochemical processes and cells can function like thermal machines."