High-resolution mapping of meiotic crossovers and non-crossovers in yeast

Meiotic recombination has a central role in the evolution of sexually reproducing organisms. The two recombination outcomes, crossover and non-crossover, increase genetic diversity, but have the potential to homogenize alleles by gene conversion. Whereas crossover rates vary considerably across the genome, non-crossovers and gene conversions have only been identified in a handful of loci. To examine recombination genome wide and at high spatial resolution, we generated maps of crossovers, crossover-associated gene conversion and non-crossover gene conversion using dense genetic marker data collected from all four products of fifty-six yeast (Saccharomyces cerevisiae) meioses. Our maps reveal differences in the distributions of crossovers and non-crossovers, showing more regions where either crossovers or non-crossovers are favoured than expected by chance. Furthermore, we detect evidence for interference between crossovers and non-crossovers, a phenomenon previously only known to occur between crossovers. Up to 1% of the genome of each meiotic product is subject to gene conversion in a single meiosis, with detectable bias towards GC nucleotides. To our knowledge the maps represent the first high-resolution, genome-wide characterization of the multiple outcomes of recombination in any organism. In addition, because non-crossover hotspots create holes of reduced linkage within haplotype blocks, our results stress the need to incorporate non-crossovers into genetic linkage analysis.     

Reduced sleep in Drosophila Shaker mutants

Most of us sleep 7-8 h per night, and if we are deprived of sleep our performance suffers greatly; however, a few do well with just 3-4 h of sleep-a trait that seems to run in families. Determining which genes underlie this phenotype could shed light on the mechanisms and functions of sleep. To do so, we performed mutagenesis in Drosophila melanogaster, because flies also sleep for many hours and, when sleep deprived, show sleep rebound and performance impairments. By screening 9,000 mutant lines, we found minisleep (mns), a line that sleeps for one-third of the wild-type amount. We show that mns flies perform normally in a number of tasks, have preserved sleep homeostasis, but are not impaired by sleep deprivation. We then show that mns flies carry a point mutation in a conserved domain of the Shaker gene. Moreover, after crossing out genetic modifiers accumulated over many generations, other Shaker alleles also become short sleepers and fail to complement the mns phenotype. Finally, we show that short-sleeping Shaker flies have a reduced lifespan. Shaker, which encodes a voltage-dependent potassium channel controlling membrane repolarization and transmitter release, may thus regulate sleep need or efficiency.     

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Das Spitzenwachstum der Fasern beiLinum perenne L

Summary In shoots ofLinum perenne apical growth was observed at both ends of the fibres. Their rounded tips, rich in protoplasm, protude into the middle lamellae of adjacent fibres or parenchyma cells. In addition to their apical growth, the fibre walls undergo symplastic growth with the walls of neighbouring cells. The formation of the pointed ends of fully developed fibres is described.     

Fasergabelung durch Auftreten lokalisierter Wachstumsbezirke

Summary The formation of forked fibres cannot be explained by the theories of sliding or of symplastic growth, while the theory of local apical growth of fibre ends accounts for all the actual facts observed in xylem and phloem fibres ofSparmannia africana. In this species cambium cells with a split end are found. These cells give rise to forked fibres, the forking point of which does not show any sliding growth, but remains on its original level. This evidence is undoubtedly a proof against the theory of sliding growth during fibre elongation inSparmannia.     

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Three-dimensional structure of annexins

Annexins constitute a family of structurally related calcium- and phospholipid-binding proteins whose molecular structure has been investigated in detail in the crystalline and membrane-bound form. Their polypeptide chain is folded into four or eight α-helical domains of similar structure with a central hydrophilic pore. Bound to phospholipid membranes, the four-domain arrangement of the annexin molecule is conserved. A peripheral binding mode has been well documented by electron microscopy and a variety of other techniques.     

An Algorithm for Computing Cutpoints in Finite Metric Spaces

The theory of the tight span, a cell complex that can be associated to every metric D, offers a unifying view on existing approaches for analyzing distance data, in particular for decomposing a metric D into a sum of simpler metrics as well as for representing it by certain specific edge-weighted graphs, often referred to as realizations of D. Many of these approaches involve the explicit or implicit computation of the so-called cutpoints of (the tight span of) D, such as the algorithm for computing the “building blocks” of optimal realizations of D recently presented by A. Hertz and S. Varone. The main result of this paper is an algorithm for computing the set of these cutpoints for a metric D on a finite set with n elements in O(n3) time. As a direct consequence, this improves the run time of the aforementioned O(n6)-algorithm by Hertz and Varone by “three orders of magnitude”.