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Arbeithuber, B.

Publications and source records attributed to Arbeithuber, B..

2 recordsLinked to original sources

Length asymmetry and heterozygosity strongly influences the evolution of poly-A microsatellites at meiotic recombination hotspots

Meiotic recombination has strong, but poorly understood, effects on short tandem repeat (STR) instability. Here, we screened thousands of single recombinant products to characterize the transmission and evolution of polymorphic poly-A repeats at a human recombination hotspot. We show that length asymmetry between heterozygous poly-As plays a key role in the recombination outcome and their transmission. A difference of 10 As (9A/19A) elevates the frequency of non-crossovers, complex recombination products, and long conversion tracts. Moreover, asymmetry also influences STR transmission: the shorter allele is transmitted more frequently (deletion bias) at the asymmetric STR (9A/19A), while the longer allele is favored (insertion bias) at the site with a small STR length difference (6A/7A). Finally, potentially due to this opposing insertion/deletion driven evolution, we find that poly-As are enriched at human recombination hotspots predominantly with short poly-As, possibly influencing open chromatin regions that in turn can activate hotspots.

evolutionary biology

A high resolution view of adaptive events

Coadaptation between bacterial hosts and plasmids often involves a small number of highly reproducible mutations. Yet little is known about the underlying complex dynamics that leads to such a single \"correct\" solution. Observing mutations in fine detail along the adaptation trajectory is necessary for understanding this phenomenon. We studied coadaptation between E. coli and a common artificial plasmid, pBR322, in a continuous turbidostat culture. To obtain a high resolution picture of early adaptive events, we used a highly sensitive duplex sequencing strategy to directly observe and track mutations with frequencies undetectable with conventional methods. The observed highly reproducible trajectories are governed by clonal interference and show rapid increases in the frequencies of beneficial mutations controlling plasmid replication followed by a profound diversity crash corresponding to the emergence of chromosomal variants. To the best of our knowledge our study represents the first comprehensive assessment of adaptive processes at a very fine level of resolution. Our work highlights the hidden complexity of coadaptation, and provides an experimental and theoretical foundation for future studies.

evolutionary biology