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Khristich, A. N.

Publications and source records attributed to Khristich, A. N..

2 recordsLinked to original sources

An empirical long-term competition among natural yeast isolates reveals that short-term fitness largely but not entirely predicts long-term outcomes

The fitness of an organism determines its likelihood of succeeding in short-term competition, but many other factors can influence its long-term success. In this study, we investigate the relative contribution of initial fitness to a strain's long-term success in a naturally diverse population. Specifically, we compete a pool of 282 genetically barcoded S. cerevisiae isolates for up to 720 generations in six distinct environments. We find that the strains that remain at detectable frequency until the end of the competition uniformly come from the initially fittest top 5% of strains, rendering initial fitness a strong predictor of long-term success. However, small fitness differences among the top strains matter little for their long-term evolutionary fate. Indeed, we often see heterogeneity in the competition outcomes across replicates, suggesting that stochastic, large-effect adaptive mutations overwrite small differences in the initial fitness of the highest fitness strains. In addition, our results hint that evolvability differences might result in certain strains consistently over- or underperforming in the competition. We further demonstrate that the "finalists" of our competition accumulate a diverse spectrum of de novo genetic changes: single nucleotide mutations, indels, whole chromosome losses and amplifications, and widespread losses of heterozygosity that occasionally span hundreds of kilobases. Taken together, we show that for a pool of natural strains, high initial fitness is necessary, though not sufficient, to succeed long-term, and that adaptive evolution can drive unexpected outcomes in a long-term competition in a novel environment.

evolutionary biology↗

DNA Nicks Drive Massive Expansions of (GAA)n Repeats

Over 50 hereditary degenerative disorders are caused by expansions of short tandem DNA repeats (STRs). (GAA)n repeat expansions are responsible for Friedreichs ataxia as well as late-onset cerebellar ataxias (LOCAs). Thus, the mechanisms of (GAA)n repeat expansions attract broad scientific attention. To investigate the role of DNA nicks in this process, we utilized a CRISPR-Cas9 nickase system to introduce targeted nicks adjacent to the (GAA)n repeat tract. We found that DNA nicks 5 of the (GAA)100 run led to a dramatic increase in both the rate and scale of its expansion in dividing cells. Strikingly, they also promoted large-scale expansions of carrier- and large normal-size (GAA)n repeats, recreating, for the first time in a model system, the expansion events that occur in human pedigrees. DNA nicks 3 of the (GAA)100 repeat led to a smaller but significant increase in the expansion rate as well. Our genetic analysis implies that in dividing cells, conversion of nicks into double-strand breaks (DSBs) during DNA replication followed by DSB or fork repair leads to repeat expansions. Finally, we showed that 5 strand nicks increase expansion frequency in non-dividing yeast cells, albeit to a lesser extent that in dividing cells.

molecular biology↗