It is difficult to directly observe processes like natural selection at the genetic level, but relatively easy to estimate genetic frequencies in populations. As a result, genetic frequency data are widely used to make inferences about the underlying evolutionary processes. However, multiple processes can generate the same patterns of frequency data, making such inferences weak. By studying the limits to the underlying processes, one can make inferences from frequency data by asking how strong selection (or some other process of interest) would have to be to generate the observed pattern. Here we present results of a study of the limits to the relationship between selection and recombination in two-locus, two-allele systems in which we found the limiting relationships for over 30000 sets of parameters, effectively covering the range of two-locus, two-allele problems. Our analysis relates T(min)--the minimum time for a population to evolve from the initial to the final conditions--to the strengths of selection and recombination, the amount of linkage disequilibrium, and the Nei distance between the initial and final conditions. T(min) can be large with either large disequilibrium and small Nei distance, or the reverse. The behavior of T(min) provides information about the limiting relationships between selection and recombination. Our methods allow evolutionary inferences from frequency data when deterministic processes like selection and recombination are operating; in this sense they complement methods based entirely on drift.
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http://dx.doi.org/10.1006/bulm.2002.0324 | DOI Listing |
Proc Natl Acad Sci U S A
January 2025
Laboratory of Obesity and Aging Research, Cardiovascular Branch, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892.
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View Article and Find Full Text PDFAlzheimers Dement
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University of California San Francisco, San Francisco, CA, USA.
Background: The direct and chaperone-associated interactions of E3 ubiquitin ligase CHIP with tau in Alzheimer's disease and other tauopathies, regulates tau turnover, by directly linking it to ubiquitination and proteasomal degradation, as well as through suppression of tau aggregation. Modulation of these CHIP-driven tau clearance mechanisms can be an effective treatment strategy. Antigen-binding antibody fragments (Fabs) are potent tools that can highly-selectively engage target proteins and act as functional probes or inhibitors.
View Article and Find Full Text PDFMol Biol Evol
January 2025
Swiss Institute of Bioinformatics, Basel, Switzerland.
Bacterial genomes primarily diversify via gain, loss, and rearrangement of genetic material in their flexible accessory genome. Yet the dynamics of accessory genome evolution are very poorly understood, in contrast to the core genome where diversification is readily described by mutations and homologous recombination. Here, we tackle this problem for the case of very closely related genomes.
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January 2025
Department of Biology and Wildlife, University of Alaska Museum, Fairbanks, Alaska, USA.
The application of high-throughput sequencing to phylogenetic analyses is allowing authors to reconstruct the true evolutionary history of species. This work can illuminate specific mechanisms underlying divergence when combined with analyses of gene flow, recombination and selection. We conducted a phylogenomic analysis of Catharus, a songbird genus with considerable potential for gene flow, variation in migratory behaviour and genomic resources.
View Article and Find Full Text PDFBiochemistry
January 2025
Department of Pharmaceutical Sciences, University of Shizuoka, Shizuoka 422-8526, Japan.
DtpC was isolated from the ditryptophenaline biosynthetic pathway found in filamentous fungi as a cytochrome P450 (P450) that catalyzes the dimerization of diketopiperazines. More recently, several similar P450s were discovered. While a vast majority of such P450s generate asymmetric diketopiperazine dimers, DtpC and other fungal P450s predominantly catalyze the formation of symmetric dimer products.
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