Back

Evolution of the highest fidelity DNA replication systems

Baehr, S.; Call, C.

2026-04-17 molecular biology
10.64898/2026.04.16.719065 bioRxiv
Show abstract

DNA mutation on average is deleterious, and evolution generally acts to reduce mutation rates to the limit of natural selection. The limit of natural selection is set by multiple factors, of which effective population size is only one. We consider a form of lethal mutagenesis as an upper bound to mutation rates for any organism, an argument that is congruent with a biophysical context, wherein random mutations are a form of entropy. In this analysis, coding genome size, body mass, generation time, and temperature explain more than 90% of the variation in mutation rate per generation across the Tree of Life. The organisms with larger genomes, longer lifespans and relatively larger body sizes, known and unknown, represent the lineages which have likely evolved novel mechanisms to lower mutation rates. Though these variables are largely shared by Petos Paradox, this selective pressure occurs through germline mutation rate evolution rather than the soma. SignificanceDNA replication is a trait subject to variation and natural selection. DNA mutation on average is deleterious, and is a major contributor to human disease. Lower mutation rates are of general interest to humans, who suffer from age-related diseases such as cancer, and who also now enjoy longer average generation times which generate more random mutations between generations. By identifying the general themes compelling the evolution of DNA replication fidelity, molecular mechanisms to lower human DNA mutation rates may be more efficiently sought.

Matching journals

The top 9 journals account for 50% of the predicted probability mass.

50% of probability mass above

"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.