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Wahl, N.

Publications and source records attributed to Wahl, N..

2 recordsLinked to original sources

Phylogenetic reconciliation supports a methanogenic ancestor of the Archaea and a derived origin for host-associated lineages

The phylogeny of the Archaea continues to be revisited and revised as new groups are discovered and phylogenetic methods improve, but key questions about their early evolution remain. It has been suggested that the root of the Archaea may lie on, or potentially within, any of three major groups - the Euryarchaeota, TACK+Asgard clade, and DPANN, the last of which includes many host-associated and genome-reduced lineages. These root hypotheses make starkly different predictions about the nature of early archaeal evolution: for example, a root on or within DPANN might suggest a small-genome and host-associated ancestor, with methanogenesis, the hallmark metabolism of the Archaea, evolving later. Here, we investigate the position of the archaeal root and the nature of the last archaeal common ancestor using a range of phylogenetic approaches, including the best available site- and branch-heterogeneous substitution models, and new gene tree-species tree reconciliation models that capture changes in rates of gene duplication, loss and transfer across the phylogeny. Our analyses converge on a narrow archaeal root region at/near the base of the Euryarchaeota, supporting hypotheses in which the Last Archaeal Common Ancestor (LACA) was a complex, free-living (hyper-)thermophilic methanogen. We recover DPANN as the sister group to TACK and Asgard archaea, and suggest that their genome evolution has been characterised by episodes of genome streamlining and expansion, driven by gene loss and transfer.

evolutionary biology↗

SATB2 organizes the 3D genome architecture of cognition in cortical neurons

SATB2 is genetically associated with human intelligence. Since SATB2 protein structure predicts a function in DNA looping, we analyzed the impact of SATB2 on 3D genome architecture and chromatin accessibility in cortical neurons. Our data reveal strong effects of SATB2 on chromatin looping between enhancers and promoters of neuronal activity-regulated genes, which closely correlate with gene expression. We furthermore identify SATB2-dependent alterations at all 3D genome architectural levels, including compartments, Topologically Associated Domains and Frequently Interacting Regions. Genes linked to SATB2-dependent 3D genome changes are implicated in highly specialized neuronal functions and contribute to cognitive ability and risk for neuropsychiatric and neurodevelopmental disorders. The altered non-coding regions are enriched for common variants associated with educational attainment, intelligence and schizophrenia. Our data establish SATB2 as a 3D genome organizer, which operates both independently and in cooperation with CTCF to set up the chromatin landscape of pyramidal neurons for cognitive processes.

neuroscience↗