Uncovering Clues to a Natural Gene-Editing Technique

Diversity-generating retroelements (DGRs) are mechanisms that allow microbes to edit their genes. This illustrates a ribonucleoprotein within a DGR. Credit: Blair Paul, generated from an RNP structure in Handa et al., using Protein Data Bank Japan (PDBJ)

Most evolutionary change happens slowly, over many generations. Through the process of natural selection, random genetic mutations that give individuals a survival advantage are passed on to their descendants, and the species gradually evolves.

But sometimes, evolution has an accelerated timeline and a gene changes very quickly, likely in response to sudden environmental change. One cause of accelerated evolution is a mechanism called diversity-generating retroelements (DGR).

DGRs are found in the genomes of microorganisms across the globe鈥攆rom the arctic permafrost to Yellowstone鈥檚 hot springs and the human gut. DGRs can reverse-transcribe RNA back to DNA in a form of natural gene-editing. This process speeds up the evolution of proteins to help microorganisms adapt to changing environments.

Marine Biological Laboratory (美女直播做爱) Assistant Scientist Blair Paul is a co-author on a new paper that sheds light on this process. The study deepens our understanding of the evolutionary origin of DGRs, and may be applicable to future gene-editing techniques.

Paul collaborated with Partho Ghosh鈥檚 lab at the University of California, San Diego, which figured out the first steps of this accelerated evolution by visualizing the relevant proteins and RNA in DGRs using cryogenic electron microscopy. They found that RNA especially controlled accelerated evolution, forming structures that started, maintained and stopped the process at the right place. These RNA structures, which were identified in the DGRs of many microorganisms, limited accelerated evolution to proteins needed for adaptation while protecting other essential proteins from harm.

鈥淧rior to this, we really didn鈥檛 know much about the structural function of the RNA in a DGR,鈥 Paul said. 鈥淲e knew next to nothing about it.鈥

Paul compared their model DGR with roughly 300 other bacterial and archaeal DGRs. He found that about 75 percent of these DGRs shared structural RNA features with the model.

鈥淚t鈥檚 possible these RNA features first appeared in DGRs in common ancestors, rather than independently evolving in different bacteria,鈥 Paul said. 鈥淏ut it鈥檚 hard to say: we just get this one snapshot in time."

Paul鈥檚 research group is studying DGRs at the 美女直播做爱, particularly in multicellular cyanobacteria. Studies like this one could potentially help scientists engineer DGRs for applications like directed evolution or gene-editing technologies.

鈥淲ithout these structural insights about how the RNA actually coordinates this, you may face limitations in trying to engineer this system,鈥 Paul said.

Citation: Handa, S., Biswas, T., Chakraborty, J., Ghosh, G., Paul, B., & Ghosh, P. (2025). RNA control of reverse transcription in a diversity-generating retroelement. Nature, DOI: