For the emergence of early life, the formation of biopolymers such as RNA is essential. However, the addition of nucleotide monomers to existing oligonucleotides requires millimolar concentrations. Even in such optimistic settings, no polymerization of RNA longer than about 20 bases could be demonstrated. How then could self-replicating ribozymes appear, for which recent experiments suggest a minimal length of 200 nt? Here, we demonstrate a mechanism to bridge this gap: the escalated polymerization of nucleotides by a spatially confined thermal gradient. The gradient accumulates monomers by thermophoresis and convection while retaining longer polymers exponentially better. Polymerization and accumulation become mutually self-enhancing and result in a hyperexponential escalation of polymer length. We describe this escalation theoretically under the conservative assumption of reversible polymerization. Taking into account the separately measured thermophoretic properties of RNA, we extrapolate the results for primordial RNA polymerization inside a temperature gradient in pores or fissures of rocks. With a dilute, nanomolar concentration of monomers the model predicts that a pore length of 5 cm and a temperature difference of 10 K suffice to polymerize 200-mers of RNA in micromolar concentrations. The probability to generate these long RNAs is raised by a factor of >10 600 compared with polymerization in a physical equilibrium. We experimentally validate the theory with the reversible polymerization of DNA blocks in a laser-driven thermal trap. The results confirm that a thermal gradient can significantly enlarge the available sequence space for the emergence of catalytically active polymers. molecular evolution | nonequilibrium | RNA world | (nonenzymatic) emergence of RNA | hydrothermal vents P olymers are the vital building blocks of all known life forms. According to the central dogma of molecular biology (1), DNA stores the information for how and when to build proteins, which for their part carry out catalytic tasks like the polymerization of DNA. How this self-perpetuating cycle has started is unknown. The RNA-world hypothesis posits that RNA molecules were the central players in prebiotic evolution, because they exhibit both a catalytic function similar to that of proteins and the information storage capabilities of DNA (2). However, how could such an RNA world have emerged from the prebiotic soup?A key element of the RNA world is a ribozyme that catalyzes RNA replication. Directed in vitro evolution and engineering have shown that such ribozymes exist, but require a length of 200 bases or more, even in favorable high-salt conditions (3). Starting from chemical nonequilibrium conditions with millimolar concentrations of energy-rich nucleotides (4-6) and with the help of catalytic surfaces (7), only the formation of much shorter polynucleotides on the order of 20 bases was demonstrated in the laboratory. Slow kinetics and cleavage due to hydrolysis limit the formation of long polynucleotides and finally lead...

The hallmark of living matter is the replication of genetic molecules and their active storage against diffusion. We implement both in the simple nonequilibrium environment of a temperature gradient. Convective flow both drives the DNA replicating polymerase chain reaction while concurrent thermophoresis accumulates the replicated 143 base pair DNA in bulk solution. The time constant for accumulation is 92 s while DNA is doubled every 50 s. The experiments explore conditions in pores of hydrothermal rock which can serve as a model environment for the origin of life.

Non-equilibrium conditions must have been crucial for the assembly of the first informational polymers of early life-by supporting their formation and continuous enrichment in a long-lasting environment. Here we explored how gas bubbles in water subjected to a thermal gradient, a likely scenario within crustal mafic rocks on the early Earth, drive a complex, continuous enrichment of prebiotic molecules. RNA precursors, monomers, active ribozymes, oligonucleotides, and lipids are shown to (1) cycle between dry and wet states, enabling the central step of RNA phosphorylation, (2) accumulate at the gas-water interface to drastically increase ribozymatic activity, (3) condense into hydrogels, (4) form pure crystals, and (5) encapsulate into protecting vesicle aggregates that subsequently undergo fission. These effects occurred within less than 30 minutes. The findings unite physical conditions in one location which were crucial for the chemical emergence of biopolymers.They suggest that heated microbubbles could have hosted the first cycles of molecular evolution.Life is a non-equilibrium system. By evolution, modern life has created a complex protein machinery to maintain the nonequilibrium of crowded molecules inside dividing vesicles. Based on entropy arguments, equilibrium conditions were unlikely to trigger the evolutionary processes during the origin of life 1 . External non-equilibria had to be provided for the accumulation, encapsulation, and replication of the first informational molecules. They can locally reduce entropy, give rise to patterns 2 , and lean the system towards a continuous, dynamic self-organization 3 . Non-equilibrium dynamics can be found in many fluid systems, including gravity-driven instabilities in the atmosphere 4 , the accumulation of particles in nonlinear flow 5,6 , and shear-dependent platelet activation in blood 7 . Our experiments discuss whether gas-water interfaces in a thermal gradient could have provided such a nonequilibrium setting for the emergence of life on early Earth.Non-equilibrium systems in the form of heat flows were a very common and simplistic setting, found ubiquitously on the planet 8 . Hydrothermal activity is considered abundant on early Earth and intimately linked to volcanic activity 9 . Water is thereby circulating through the pore space of the volcanic rocks, which is formed by magmatic vesiculation (primary origin) and fractures (secondary origin). These systems have been studied as non-equilibrium driving forces for biological molecules in a variety of processes 10-17 .Gases originating from degassing of deeper magma bodies percolate through these water-filled pore networks. At shallow depths bubbles are formed by gases dissolved in water and formation of vapor where sufficient heat is supplied by the hydrothermal system. The bubbles create gas-water interfaces, which previously have been discussed in connection with atmospheric bubble-aerosol-droplet cycles 18 , the adsorption of lipid monolayers and DNA to the interface 19,20 , or the formation of pep...

Recent progress in the synthesis of nucleotides from prebiotically plausible precursors has opened up new ways to explain the origin of genetic matter. Mechanisms for the polymerization of nucleotides without the help of catalysts are, however, rare. Complementary to the experiments done by Costanzo et al., we found that drying 3',5'-cyclic GMP leads to poly-G RNA strands with lengths of up to 40 nucleotides. We also show that the polymerization to long RNA strands is considerably more efficient under dry conditions than for cGMP polymerization in water. The length depends on the incubation time of dry nucleotides at temperatures of 40-80 °C. No enzymes or other catalysts are needed for successful polymerization.