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Aldridge, M.

Publications and source records attributed to Aldridge, M..

2 recordsLinked to original sources

Metagenomic prediction of methane emissions in sheep using single- and multi-matrix BLUP models with taxonomic and functional microbial features

BackgroundEnteric methane emissions from ruminant livestock represent a major greenhouse gas contributor, yet identification of high- and low-emitting ruminants remains expensive and logistically challenging for agricultural methane mitigation strategies. Ruminal microbial profiles derived from long-read sequencing technology provide a potential proxy to predict methane production. The optimal bioinformatic pipelines for processing long-read metagenomic data to perform methane predictions have yet to be determined. Here we evaluated how different metagenomic analysis pipelines affect methane predictive model accuracy in grazing sheep. ResultsWe applied three bioinformatic pipelines to characterize the taxonomic and functional features of rumen microbiomes from 396 sheep. Functional abundance features were annotated from Clusters of Orthologous Genes (COG) or Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. The single-matrix model using COG features achieved the highest microbiability (m2 = 0.942: proportion of variance component explained by microbial features) and predictive accuracy (5-fold cross validation r = 0.609: Pearsons correlation between predicted and observed values). Both functional features outperformed all taxonomic features across all three pipelines in predictive accuracy. The multi-matrix models combined functional and taxonomic features slightly improved methane predictive accuracy across both 5-fold cross-validation and leave-one-day-out validation compared to the models using functional features alone. ConclusionsThese findings demonstrate the potential advantages of using long-read metagenomic data to predict enteric methane emissions in ruminants. COG-based functional features achieved the highest predictive accuracy among all feature types, suggesting that functional annotation of existing long-read sequences is sufficient for accurate methane prediction without requiring complementary taxonomic data.

genomics↗

Repeat associated non-AUG translation as a common mechanism for the polyGln ataxias

Determining if repeat associated non-AUG (RAN) proteins contribute to the CAG polyGln-encoding spinocerebellar ataxias (CAG-SCAs) is critical for understanding mechanisms and developing therapies for these diseases. Immunohistochemistry using antibodies against polySer and polyLeu repeats and locus specific C-terminal regions show sense polySer (AGC frame) and antisense polyLeu (CUG frame) RAN proteins accumulate in affected grey and white-matter brain regions, throughout the cerebellum and pons, in SCA1, SCA2, SCA3, SCA6, and SCA7 autopsy brains. Cerebellar white matter regions with prominent polySer and polyLeu but minimal polyGln aggregates show demyelination, white matter loss, and activated microglia. In SCA3 mice, RAN proteins accumulate in an age-dependent manner. In neural cells, polySer and polyLeu RAN proteins are toxic and cause autophagic dysfunction. In cells, the FDA-approved drug metformin decreases RAN protein levels and reduces toxicity. Taken together, these data identify sense and antisense RAN proteins as a common molecular mechanism shared by the CAG-SCAs.

neuroscience↗