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Rivals, E.

Publications and source records attributed to Rivals, E..

3 recordsLinked to original sources

Algorithms to reconstruct past indels: the deletion-only parsimony problem

Ancestral sequence reconstruction is an important task in bioinformatics, with applications ranging from protein engineering to the study of genome evolution. When sequences can only undergo substitutions, optimal reconstructions can be efficiently computed using well-known algorithms. However, accounting for indels in ancestral reconstructions is much harder. First, for biologically-relevant problem formulations, no polynomial-time exact algorithms are available. Second, multiple reconstructions are often equally parsimonious or likely, making it crucial to correctly display uncertainty in the results. Here, we consider a parsimony approach where any indel event has the same cost, irrespective of its size or the branch where it occurs. We thoroughly examine the case where only deletions are allowed, while addressing the aforementioned limitations. First, we describe an exact algorithm to obtain all the optimal solutions. The algorithm runs in polynomial time if only one solution is sought. Second, we show that all possible optimal reconstructions for a fixed node can be represented using a graph computable in polynomial time. While previous studies have proposed graph-based representations of ancestral reconstructions, this result is the first to offer a solid mathematical justification for this approach. Finally we discuss the relevance of the deletion-only case for the general case. Author summaryAn exciting frontier in evolutionary biology is the ability to reconstruct DNA or protein sequences from species that lived in the distant past. By analyzing sequences from present-day species, we aim to infer the sequences of their common ancestors --a process known as ancestral sequence reconstruction. This task has far-reaching applications, such as resurrecting ancient proteins and studying the biology of extinct organisms. However, a significant challenge remains: the lack of well-established methods for inferring past deletions and insertions ---mutations that remove or add segments of genetic code. In this paper, we present algorithms that lay the groundwork for addressing this gap. We show that finding the reconstructions involving only deletion events, while minimizing their number, can be done efficiently. Additionally, we show that all optimal solutions can be represented using specialized graphs. While previous studies have proposed graph-based representations of ancestral reconstructions, we are the first to provide a rigorous mathematical foundation for the use of these graphs.

bioinformatics↗

Rapid screening and detection of inter-type viral recombinants using phylo-k-mers

MotivationNovel recombinant viruses may have important medical and evolutionary significance, as they sometimes display new traits not present in the parental strains. This is particularly concerning when the new viruses combine fragments coming from phylogenetically-distinct viral types. Here, we consider the task of screening large collections of sequences for such novel recombinants. A number of methods already exist for this task. However, these methods rely on complex models and heavy computations that are not always practical for a quick scan of a large number of sequences. ResultsWe have developed SHERPAS, a new program to detect novel recombinants and provide a first estimate of their parental composition. Our approach is based on the precomputation of a large database of "phylogenetically-informed k-mers", an idea recently introduced in the context of phylogenetic placement in metagenomics. Our experiments show that SHERPAS is hundreds to thousands of times faster than existing software, and enables the analysis of thousands of whole genomes, or long sequencing reads, within minutes or seconds, and with limited loss of accuracy. Availability and ImplementationThe source code is freely available for download at https://github.com/phylo42/sherpas Contactpardi@lirmm.fr, gllm.scholz@gmail.com Supplementary informationSupplementary Materials are available online.

bioinformatics↗

NF-Y Controls Fidelity of Transcription Initiation at Gene Promoters Through Maintenance of the Nucleosome-Depleted Region

Faithful transcription initiation is critical for accurate gene expression, yet the mechanisms underlying specific transcription start site (TSS) selection in mammals remain unclear. Here, we show that the histone-fold domain protein NF-Y, a ubiquitously expressed transcription factor, controls the fidelity of transcription initiation at gene promoters. We report that NF-Y maintains the region upstream of TSSs in a nucleosome-depleted state while simultaneously protecting this accessible region against aberrant and/or ectopic transcription initiation. We find that loss of NF-Y binding in mammalian cells disrupts the promoter chromatin landscape, leading to nucleosomal encroachment over the canonical TSS. Importantly, this chromatin rearrangement is accompanied by upstream relocation of the transcription preinitiation complex and ectopic transcription initiation. Further, this phenomenon generates aberrant extended transcripts that undergo translation, disrupting gene expression profiles. These results establish NF-Y as a central player in TSS selection in metazoans and highlight the deleterious consequences of inaccurate transcription initiation.

genomics↗