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Biology subjects

Fueglistaler, A.

Publications and source records attributed to Fueglistaler, A..

3 recordsLinked to original sources

SweepLink: Joint Inference of Demography and Linked~Selection from Time-series Data

Genome-wide time-series data, i.e. allele frequency trajectories tracked across multiple sampling times, are among the richest sources of information for inferring selection. Beyond a beneficial allele's own rise in frequency, such data capture how it drags nearby loci upward via linkage, an effect known as genetic hitch-hiking. Yet most existing tools are single-locus, treating loci independently: they infer site-specific selection coefficients in isolation, then rely on ad hoc window statistics to account for hitch-hiking. Many existing tools further require a predefined population size, or scale poorly when jointly inferring selection and demography, and their power is highly sensitive to a significance threshold. To address these shortcomings, we here present SweepLink, a two-layer Hidden Markov Model that overcomes these limitations by jointly inferring demography and linked selection genome-wide: a spatial layer captures correlations between neighboring selection coefficients, coupled with a temporal Wright-Fisher diffusion layer. As we show with extensive simulations, this setup pushes drift-driven false signals toward neutrality while reinforcing loci that receive support from neighbouring loci, thereby increasing the sensitivity for weak and moderate selection, while matching the power of existing tools to detect strong selection. These simulations further show that SweepLink yields confident posteriors that remain stable at maximal significance, removing the need for arbitrary thresholds. We applied SweepLink to ancient DNA time-series data from the British population, previously analysed with a single-locus tool. SweepLink recovers four of the previously reported signals (LCT, SLC45A2, DHCR7, HERC2), and partially recovers the MHC/HLA signal. It also identifies additional candidate regions, including DPYD, FADS1/2 and OAS1, missed by the prior scan but supported by independent studies.

evolutionary biology↗

Evolutionary history and genomic vulnerability of the extinct giant deer Megaloceros giganteus

The extinct giant deer (Megaloceros giganteus) was one of the most striking megafaunal species of the Late Quaternary, distinguished by its enormous palmated antlers reaching up to 3.5 m across, the largest known among both living and extinct cervids. Despite its iconic status, little is known about its genomic history prior to extinction [~]8 thousand years ago (kya). We generated the first nuclear palaeogenomes for Megaloceros, represented by nine individuals from Germany ([~]40 kya) and Ireland ([~]11 kya), mapped to a new chromosome-level reference genome of the fallow deer (Dama dama). Phylogenomic analyses placed Megaloceros as sister to Dama (divergence [~]3.5 Ma) and revealed evidence of gene flow with ancestral Cervus lineages. Population analyses identified clear differentiation between German and Irish lineages, with higher genetic diversity in the German individuals. Two genes under strong positive selection, BNIPL and SLC10A7, are associated with apoptosis regulation and skeletal development/bone mineralisation, respectively, and may relate to the species large body and antler size. Demographic reconstructions indicate a long-term decline in effective population size, extremely low heterozygosity, little evidence of extensive runs of homozygosity, and an elevated burden of predicted deleterious alleles. Together, these results suggest that Megaloceros entered the terminal Pleistocene in a genomically fragile state, offering new insight into the biology and evolutionary legacy of one of the largest and most distinctive cervids that ever lived.

evolutionary biology↗

Designed allosteric biosensors for engineered T cell therapy of cancer

Adoptive cell therapy with chimeric antigen receptor (CAR) T cells has transformed standard-of-care for selected hematologic malignancies, but relapses are frequent and efficacy against solid tumors remains limited1,2. The tumor microenvironment (TME) plays a key role in tumor progression3, and both soluble and cellular TME components can limit CAR-T cell function and persistence4. Targeting soluble TME factors to enhance anti-tumor responses of engineered T cells through chimeric receptors is not yet broadly explored due to the unpredictable signaling characteristics of synthetic protein receptors. Here we developed a protein design platform for the de novo bottom-up assembly of allosteric receptors with programmable input-output behaviors that respond to soluble TME factors with co-stimulation and cytokine signals in T cells, called T-SenSER (TME-sensing switch receptor for enhanced response to tumors). We developed two sets of T-SenSERs targeting vascular endothelial growth factor (VEGF) or colony stimulating factor 1 (CSF1), that are both selectively enriched in a variety of tumors. Combination of CAR and T-SenSER in human T cells enhanced anti-tumor responses in models of lung cancer and multiple myeloma, in a VEGF or CSF1-dependent manner. Our study sets the stage for the accelerated development of synthetic biosensors with custom-built sensing and responses for basic and translational cell engineering applications.

bioengineering↗