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Ellison, S.

Publications and source records attributed to Ellison, S..

5 recordsLinked to original sources

Ancestry and Environmental Adaptation in North American Feral Cannabis

Understanding how different populations respond to environmental variation is fundamental to breeding climate resilient crops. In this study, we integrate three diverse georeferenced Cannabis datasets comprising North American feral populations and Eurasian samples (n=909) to resolve population structure, infer evolutionary relationships and quantify adaptive responses to climate across a broad environmental gradient. Phylogenetic analysis rooted to Humulus lupulus shows North American feral populations are more closely related to basal and hemp-type lineages than to drug-type or Iranian populations, a pattern supported by ancestry and PCA analyses. By combining these datasets, we capture a wider range of climatic variation and gain new insight into the adaptive potential of cannabis germplasm. Using environmental genomic selection (EGS), we identified nine bioclimatic traits with prediction accuracies exceeding 0.5 across the combined datasets (12,030 SNPs; 909 samples; training = 191). When analyzing the North American dataset alone, EGS revealed 14 traits with prediction accuracies greater than 0.85 (22,852 SNPs; 760 samples; training = 310). Genomic estimated adaptive values (GEAVs) revealed population specific climatic responses, particularly for precipitation related traits, with northeastern North American populations (Indiana and New York) showing signatures consistent with adaptation to wetter and cooler environments. Climate projections under a high emission scenario (SSP585) indicate that [~]34 % of sampled locations are expected to transition to different Koppen-Geiger climate classes by 2050, with distinct shifts observed among North American and Iranian populations. Genome environment association (GEA) analysis identified replicated temperature and precipitation associated loci across multiple chromosomes. Using genotype-phenotype data, genomic selection for cannabinoid traits revealed that only CBD achieved prediction accuracies exceeding 0.5, consistent with a polygenic architecture extending beyond the CBDAS locus. Collectively, these results demonstrate that feral and landrace Cannabis populations harbor substantial adaptive variation and represent an underutilized reservoir for climate resilient breeding and allele discovery, with relevance for pre-breeding efforts under future climate scenarios.

plant biology↗

Structure and sequence evolution in the pennycress (Thlaspi arvense) pangenome

O_LIEukaryotic genomes harbor many forms of variation, including nucleotide diversity and structural polymorphisms, which experience natural selection and contribute to genome evolution and biodiversity. However, harnessing this variation for agriculture hinges on our ability to detect, quantify, catalog, and utilize genetic diversity. C_LIO_LIHere, we explore seven complete genomes of the emerging biofuel crop pennycress (Thlaspi arvense) drawn from across the speciess current genetic diversity to catalogue variation in genome structure and content. C_LIO_LIAcross this new pangenome resource, we find contrasting evolutionary modes in different genomic regions. Gene-poor, repeat-rich pericentromeric regions experience frequent rearrangements, including repeated centromere repositioning. In contrast, conserved gene-dense chromosome arms maintain large-scale synteny across accessions, even in fast-evolving immune genes where microsynteny breaks down across species but the macrosynteny of gene cluster positioning is maintained. C_LIO_LIOur findings highlight that multiple elements of the genome experience dynamic evolution that conserves functional content on the chromosome scale but allows rearrangement and presence-absence variation on a local scale. This diversity is invisible to classical reference-based approaches and highlights the strength and utility of pangenomic resources. These results provide a valuable case study of rapid genomic structural evolution within a species and powerful resources for crop development in an emerging biofuel crop. C_LI

genomics↗

Genetic Diversity, Population Structure, and Cannabinoid Variation in Feral Cannabis sativa Germplasm from the United States

Cannabis sativa is one of the earliest plants to be domesticated for fiber, food and medicine. Seed from Cannabis grown for industrial purposes during the 18th through 20th centuries have escaped production and established feralized populations across the United States. To maximize the potential of feral Cannabis germplasm, determining the genetic structure and cannabinoid profile is crucial for selection and breeding of new compliant regionally adapted hemp cultivars. To resolve this, a collection of feral Cannabis, comprising 760 plants across twelve US states were sequenced using Genotyping-by-Sequencings (GBS), genotyped at the cannabinoid synthase (CBDAS) gene, and subject to gas chromatography-mass spectrometry (GC-MS) to assess cannabinoid profiles. Clustering analyses by ADMIXTURE and Principal Component Analysis (PCA) stratified the germplasm into five clusters (Mississippi-River, West North Central-b, West North Central-a, New York, and Indiana). The cannabinoid genotyping assay resolved the feral collections into Type I - CXCX (6%), Type II - CFCX (15%), and Type III - CFCF (78%). Total cannabinoid content ranged from 0.21% to 4.73%. The assessment of genetic diversity, population structure, and cannabinoid profile of the US feral Cannabis collection provides critical information and germplasm resources to develop new and improve existing hemp cultivars.

plant biology↗

Atypical Protein Kinase C Promotes its own Asymmetric Localisation by Phosphorylating Cdc42 in Polarising Cells

Atypical protein kinase C (aPKC) is a major regulator of cell polarity. Acting in conjunction with Par6, Par3 and the small GTPase Cdc42, aPKC becomes asymmetrically localised and drives the polarisation of cells. aPKC activity is crucial for its own asymmetric localisation, suggesting a hitherto unknown feedback mechanism contributing to polarisation. Here we show in the C. elegans zygote that the feedback relies on aPKC phosphorylation of Cdc42 at serine 71. The turnover of CDC-42 phosphorylation ensures optimal aPKC asymmetry and activity throughout polarisation by tuning Par6/aPKC association with Par3 and Cdc42. Moreover, turnover of Cdc42 phosphorylation regulates actomyosin cortex dynamics that are known to drive aPKC asymmetry. Given the widespread role of aPKC and Cdc42 in cell polarity, this form of self-regulation of aPKC may be vital for the robust control of polarisation in many cell types. Key findings/graphical abstract- Phosphorylation of CDC-42 by aPKC accelerates aPKC dissociation from CDC-42, limiting aPKC activity - CDC-42/aPKC dissociation promotes aPKC association with PAR-3 and, thereby, aPKC asymmetry due to actomyosin flow - Cycling of CDC-42 phosphorylation fuels the exchange of aPKC between anteriorly transported PAR-3 and aPKC-active CDC-42 complexes - Turnover of CDC-42 phosphorylation alternates its association with effectors, aPKC and MRCK-1, ensuring proper actomyosin dynamics O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=136 SRC="FIGDIR/small/563985v2_ufig1.gif" ALT="Figure 1"> View larger version (43K): org.highwire.dtl.DTLVardef@e0ec65org.highwire.dtl.DTLVardef@c00b8dorg.highwire.dtl.DTLVardef@36565dorg.highwire.dtl.DTLVardef@160149a_HPS_FORMAT_FIGEXP M_FIG C_FIG

cell biology↗

Assessment of levamisole HCl and thymosin α1 in two mouse models of amyotrophic lateral sclerosis

Amyotrohpic lateral sclerosis (ALS) is a progressive neurodegenerative disease that causes generalized muscle weakness and atrophy. Neuropathologically, ALS is defined by severe loss of upper and lower motor neurons with a robust neuroinflammatory response. In the present study, we have examined the potential utility of two drugs that have indications as immune modulators, levamisole HCl and thymosin 1. These drugs were tested in two models models that reproduce aspects of ALS. We conducted a 14 week dosing study of these two drugs in the SOD1G93A and Prp-TDP43A315T models of ALS. The drugs were given once daily for two weeks and then every other day for 6 weeks for a total of 8 weeks of treatment. Outcome measurements included efficacy assessment on the neuromuscular phenotypes, and pathological analyses of ubiquitin load and neuro-inflammatory markers in spinal motor neurons. Neither of these drug treatments produced significant extensions in survival; however, there were changes in ubiquitin load in SOD1G93A mice that suggest the drugs could be beneficial as additions to other therapies.

neuroscience↗