Publications by authors named "S H Mahony"

Animal translocations provide striking examples of the human footprint on biodiversity. Combining continental-wide genomic and DNA-barcoding analyses, we reconstructed the historical biogeography of the Asian black-spined toad (Duttaphrynus melanostictus), a toxic commensal amphibian that currently threatens two biodiversity hotspots through biological invasions (Wallacea and Madagascar). The results emphasize a complex diversification shaped by speciation and mitochondrial introgression that comprises two distinct species.

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  • CCR4-NOT is a complex involved in various stages of gene regulation like transcription, mRNA decay, and protein ubiquitylation, with extensive research in yeast but limited knowledge in mammals.
  • A study using an auxin-induced degron system showed that depleting key components CNOT1 and CNOT4 in human cells led to significant changes in mRNA stability and synthesis; CNOT1 depletion increased mRNA levels while CNOT4 depletion accelerated mRNA decay.
  • The results indicated that CCR4-NOT maintains the expression of certain transcriptional repressors (KZNFs), which in turn suppress retrotransposable elements (rTEs), establishing the complex as a crucial regulator of gene expression in mammals.
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  • This systematic review evaluates the role of intraperitoneal pressure measurements in predicting complications and gastrointestinal symptoms in Peritoneal Dialysis (PD) patients suffering from End-Stage Kidney Disease (ESKD).
  • A total of 12 studies were analyzed, revealing a positive correlation between intraperitoneal pressure and Body Mass Index (BMI) and Body Surface Area (BSA), but less consistent results related to age and other factors.
  • While the findings suggest a potential link between higher intraperitoneal pressure and BMI/BSA, the impact on non-infectious complications remains unclear, with noted limitations in the studies analyzed.
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Despite the unique ability of pioneer factors (PFs) to target nucleosomal sites in closed chromatin, they only bind a small fraction of their genomic motifs. The underlying mechanism of this selectivity is not well understood. Here, we design a high-throughput assay called chromatin immunoprecipitation with integrated synthetic oligonucleotides (ChIP-ISO) to systematically dissect sequence features affecting the binding specificity of a classic PF, FOXA1, in human A549 cells.

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Transposable elements (TEs) and other repetitive regions have been shown to contain gene regulatory elements, including transcription factor binding sites. However, regulatory elements harbored by repeats have proven difficult to characterize using short-read sequencing assays such as ChIP-seq or ATAC-seq. Most regulatory genomics analysis pipelines discard "multimapped" reads that align equally well to multiple genomic locations.

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