Publications (377) View all
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Article: The recombination landscape in Arabidopsis thaliana F2 populations.
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ABSTRACT: Recombination during meiosis shapes the complement of alleles segregating in the progeny of hybrids, and has important consequences for phenotypic variation. We examined allele frequencies, as well as crossover (XO) locations and frequencies in over 7000 plants from 17 F(2) populations derived from crosses between 18 Arabidopsis thaliana accessions. We observed segregation distortion between parental alleles in over half of our populations. The potential causes of distortion include variation in seed dormancy and lethal epistatic interactions. Such a high occurrence of distortion was only detected here because of the large sample size of each population and the number of populations characterized. Most plants carry only one or two XOs per chromosome pair, and therefore inherit very large, non-recombined genomic fragments from each parent. Recombination frequencies vary between populations but consistently increase adjacent to the centromeres. Importantly, recombination rates do not correlate with whole-genome sequence differences between parental accessions, suggesting that sequence diversity within A. thaliana does not normally reach levels that are high enough to exert a major influence on the formation of XOs. A global knowledge of the patterns of recombination in F(2) populations is crucial to better understand the segregation of phenotypic traits in hybrids, in the laboratory or in the wild.Heredity 11/2011; 108(4):447-55. · 4.60 Impact Factor -
SourceAvailable from: Steve A Kay
Article: Climate Change and the Integrity of Science
P. H. Gleick, R. M. Adams, R. M. Amasino, E. Anders, D. J. Anderson, W. W. Anderson, L. E. Anselin, M. K. Arroyo, B. Asfaw, F. J. Ayala, [......], M. J. West-Eberhard, T. D. White, W. J. Wilson, R. V. Wolfenden, J. A. Wood, G. M. Woodwell, H. E. Wright, C. Wu, C. Wunsch, M. L. ZobackScience 05/2010; 328(5979):689-690. · 31.20 Impact Factor -
Article: Climate change and the integrity of science.
P H Gleick, R M Adams, R M Amasino, E Anders, D J Anderson, W W Anderson, L E Anselin, M K Arroyo, B Asfaw, F J Ayala, [......], M J West-Eberhard, T D White, W J Wilson, R V Wolfenden, J A Wood, G M Woodwell, H E Wright, C Wu, C Wunsch, M L ZobackScience 05/2010; 328(5979):689-90. · 31.20 Impact Factor -
Article: Global effects of the small RNA biogenesis machinery on the Arabidopsis thaliana transcriptome
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ABSTRACT: In Arabidopsis thaliana, four different DICER-LIKE (DCL) proteins have distinct, but partially overlapping functions in the biogenesis of microRNAs (miRNAs) and small interfering RNAs (siRNAs) from longer, non-coding precursor RNAs. To analyze the impact of different components of the small RNA (sRNA) biogenesis machinery on the transcriptome, we subjected dcl and other mutants impaired in sRNA biogenesis to whole-genome tiling array analysis. We compared both protein-coding genes and non- coding transcripts, including most pri-miRNAs, in two tissues and several stress conditions. Our analysis revealed a surprising number of common targets in dcl1 and dcl2 dcl3 dcl4 triple mutants. Our results furthermore suggest that the DCL1 is not only involved in miRNA action, but also contributes to silencing of a subset of transposons, apparently through an effect on DNA methylation.Proc Natl Acad Sci U S A. 01/2010; -
Article: The rate and molecular spectrum of spontaneous mutations in Arabidopsis thaliana
S. Ossowski, K. Schneeberger, J. I. Lucas-Lledo, N. Warthmann, R. M. Clark, R. G. Shaw, D. Weigel, M. Lynch[show abstract] [hide abstract]
ABSTRACT: To take complete advantage of information on within-species polymorphism and divergence from close relatives, one needs to know the rate and the molecular spectrum of spontaneous mutations. To this end, we have searched for de novo spontaneous mutations in the complete nuclear genomes of five Arabidopsis thaliana mutation accumulation lines that had been maintained by single-seed descent for 30 generations. We identified and validated 99 base substitutions and 17 small and large insertions and deletions. Our results imply a spontaneous mutation rate of 7 x 10(-9) base substitutions per site per generation, the majority of which are G:C-->A:T transitions. We explain this very biased spectrum of base substitution mutations as a result of two main processes: deamination of methylated cytosines and ultraviolet light-induced mutagenesis.Science. 01/2010; 327(5961):92-4.