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Gill, C.

Publications and source records attributed to Gill, C..

2 recordsLinked to original sources

A conundrum of pleiotropy: GWAS-derived pleiotropy is weakly negatively associated with co-expression network centrality in Arabidopsis thaliana

Pleiotropy, the influence of a single gene on multiple phenotypic traits, is a fundamental feature of genetic systems but remains difficult to quantify at genome-wide scales. Genome-wide association studies (GWAS) provide one avenue to characterize pleiotropy through multi-trait genetic associations, while functional genomic approaches such as gene co-expression networks offer indirect predictions of gene importance and pleiotropic potential based on network centrality statistics. However, the relationship between GWAS-derived pleiotropy and network-based measures of gene importance remains unclear. Here, we quantified gene-level pleiotropy in Arabidopsis thaliana using gene-trait associations from the AraGWAS Catalog and AraPheno databases and compared them to previous estimates of pleiotropy based on gene co-expression networks. GWAS pleiotropy was measured using the Hill number of order q = 1, an entropy-based metric adapted from ecological diversity theory. Across 2,179 genes, pleiotropy exhibited a right-skewed distribution, with most genes influencing relatively few traits and a smaller subset exhibiting broad multi-trait effects. Contrary to expectations, pleiotropy was weakly negatively correlated with multiple measures of co-expression network centrality, including degree, strength, closeness, and betweenness. Additional analyses showed that GWAS-associated genes were enriched within the co-expression network, exhibited broader expression across tissues, and were modestly enriched among conserved BUSCO genes. Together, these findings reveal a conundrum: although genes identified by GWAS are broadly expressed and integrated into functional networks, the most pleiotropic genes occupy relatively peripheral positions within those networks. This unexpected pattern suggests that GWAS-derived pleiotropy captures a distinct aspect of gene function than co-expression network centrality.

evolutionary biology↗

Surviving phage attack dynamically regulates bacterial immunity to defeat counterdefenses

Transcriptional repressors with ligand-responsive WYL domains control diverse bacterial defense systems, yet the natural cues driving derepression and the physiological rationale for dynamic regulation in native host-phage contexts remain unknown. Here, we show that restricted phage infection, where defense clears a primary attack, serves as a natural cue for WYL-mediated derepression in Vibrio cholerae. Although not required to block the initial infection, this response increases defense protein abundance, shifting host-phage stoichiometry and priming surviving bacteria to overwhelm phage-encoded counterdefenses in subsequent attacks. We also find that restricted infection co-induces an unlinked anti-plasmid defense via its own WYL repressor, showing that parallel WYL sensors coordinate a broader immune response without regulatory crosstalk. In contrast, productive phage infection triggers horizontal transfer of the defense-encoding mobile element, ensuring its persistence in the population. Together, our work reveals that infection fate dictates divergent outcomes for the expression and dissemination of bacterial immunity.

microbiology↗