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Levene, S. D.

Publications and source records attributed to Levene, S. D..

5 recordsLinked to original sources

A Distinct Mode of Chromosome-End Genome Instability Revealed by Circulome Characterization and Analyses

Genome instability is a central hallmark of cancer and it is characterized largely from sequence: mutation, copy-number change and rearrangement scored against a linear reference. The genome has additional degrees of freedom, such as the physical form (topology) of the DNA itself. A specific mode of localized genome dynamics changes both dimensions (sequence and topology) at once: defined chromosomal regions are also represented as extrachromosomal circular DNA (eccDNA). The biogenesis of eccDNA is a feature of many cancers, supplying the tumor with genetic elements that can participate in phenotypic selection, and supplying the observer with a window into the genomic instability landscape. Genome-wide maps of where these circles arise have not been available at scale or at high resolution. Building such maps requires physical selection of circular species, because most sequenced reads from unselected DNA derive from unrearranged sequence, conflating the signal from dynamic rearrangements with that from bulk chromosomal DNA. Here we combine biophysical and biochemical isolation of circular DNA with next-generation sequencing, applying it to a panel of cancer cell lines and to patient tumors, with non-cancerous cells and adjacent normal tissues as controls. The resulting genome-wide maps of the circular-element repertoire, the Circulome, reveal a consistent and previously unreported enrichment of these elements at particular chromosome ends. The circles map to regions extending well past the telomeres, reaching varying distances up to tens of megabases inward. This activity is accompanied by corroborating rearrangements within the linear genome, consistent with regions of chromosomal instability. Together these features define a spatially localized mode of instability in cancer, which we term Erosion at Distal Genomic Ends (EDGE). We formulate a classification problem to discriminate bladder tumor from matched normal tissue, finding that the EDGE signal outperforms the mean of all interior chromosomal regions, for each chromosome. These findings define a distinct spatial signature of cancer chromosome instability detectable through Circulome analysis, and connect early models of region-specific instability to the human cancer genome.

genomics↗

Nucleosome-mediated conformational switches in micro-eccDNAs

Extrachromosomal-circular DNA (eccDNA) are circular-DNA elements that are implicated in cellular processes such as genomic diversification and instability, along with other genomic mechanisms. However, their structure and chromatinization state is poorly understood. Here we identified a 358-bp circular micro-eccDNA molecule derived from the human Titin gene, which was selected for this study based on its size and sequence characteristics, and used atomistic molecular dynamics simulations to study its interaction with nucleosomes and corresponding topological state. We show the presence or absence of bound nucleosomes provides a topological switch between intact and denatured DNA.

biophysics↗

Loop-closure Kinetics Reveal a Stable, Right-handed DNA Intermediate in Cre Recombination

In Cre site-specific recombination, the synaptic intermediate is a recombinase homotetramer containing a pair of DNA target sites. The strand-exchange mechanism proceeds via a Holliday-junction (HJ) intermediate; however, the geometry of the DNA segments in the synapse has remained highly controversial. In particular, all crystallographic structures are consistent with an achiral planar Holliday-junction (HJ) structure, whereas topological assays based on Cre-mediated knotting of plasmid DNAs are consistent with a right-handed chiral junction. Here we use the kinetics of loop closure involving closely spaced (131-151 bp), directly repeated loxP sites to investigate the in-aqueo ensemble of conformations for the longest-lived looped DNA intermediate. Fitting the experimental site-spacing dependence of the loop-closure probability, J, to a statistical-mechanical theory of DNA looping provides evidence for substantial out-ofplane HJ distortion. This result unequivocally stands in contrast to the square-planar intermediate geometry determined from crystallographic data for the Cre-loxP system and other int-superfamily recombinases. J measurements carried out with an isomerization-deficient Cre mutant suggest that the apparent geometry of the wild-type complex may result from the temporal averaging of diverse right-handed and achiral structures. Applied to Cre recombinase, and other biological systems, our approach bridges the static pictures provided by crystal structures and the natural dynamics of macromolecules in vivo. This approach thus advances a more comprehensive dynamic analysis of large nucleoprotein structures and their mechanisms.

biophysics↗

Deconvolution of Nucleic-acid Length Distributions: A Gel Electrophoresis Analysis Tool and Applications

Next-generation DNA-sequencing (NGS) technologies, which are designed to streamline the acquisition of massive amounts of sequencing data, are nonetheless dependent on various preparative steps to generate DNA fragments of required concentration, purity, and average size (molecular weight). Current automated electrophoresis systems for DNA- and RNA-sample quality control, such as Agilents Bioanalyzer (R)and TapeStation (R) products, are costly to acquire and use; they also provide limited information for samples having broad size distributions. Here we describe a software tool that helps determine the size distribution of DNA fragments in an NGS library, or other DNA sample, based on gel-electrophoretic line profiles. The software, developed as an ImageJ plug-in, allows for straightforward processing of gel images, including lane selection and fitting of univariate functions to intensity distributions. The user selects the option of fitting either discrete profiles in cases where discrete gel bands are visible, or continuous profiles, having multiple bands buried under a single broad peak. The method requires only modest imaging capabilities and is a cost-effective, rigorous alternative characterization method to augment existing techniques for library quality control.

genomics↗

Kinetic Pathways of Topology Simplification by Type-II Topoisomerases in Knotted Supercoiled DNA

The topological state of covalently closed, double-stranded DNA is defined by the knot type K and the linking-number difference {Delta}Lk relative to unknotted relaxed DNA. DNA topoisomerases are essential enzymes that control the topology of DNA in all cells. In particular, type-II topoisomerases change both K and {Delta}Lk by a duplex-strand-passage mechanism and have been shown to simplify the topology of DNA to levels below thermal equilibrium at the expense of ATP hydrolysis. It remains a puzzle how small enzymes are able to preferentially select strand passages that result in topology simplification in much larger DNA molecules. Using numerical simulations, we consider the non-equilibrium dynamics of transitions between topological states (K, {Delta}Lk) in DNA induced by type-II topoisomerases. For a biological process that delivers DNA molecules in a given topological state (K,{Delta}Lk) at a constant rate we fully characterize the pathways of topology simplification by type-II topoisomerases in terms of stationary probability distributions and probability currents on the network of topological states (K,{Delta}Lk). In particular, we observe that type-II topoisomerase activity is significantly enhanced in DNA molecules that maintain a supercoiled state with constant torsional tension. This is relevant for bacterial cells in which torsional tension is maintained by enzyme-dependent homeostatic mechanisms such as DNA-gyrase activity.

molecular biology↗