bioRxiv Science⌕ Search

Biology subjects

Lardelli, M. M.

Publications and source records attributed to Lardelli, M. M..

2 recordsLinked to original sources

tadar: an R/Bioconductor package to reduce eQTLnoise in differential expression analysis

Despite the relative maturity of bulk RNA-sequencing, compared to more recent developments such as single-cell and spatial RNA-sequencing, biases which impact data analysis continue to surface. One such bias, termed "Differential Allelic Representation" (DAR), is particularly evident when experimental samples are taken from non-isogenic genetic backgrounds. DAR is an uneven distribution of polymorphic loci between groups of experimental samples undergoing differential gene expression (DGE) analysis. When unequally represented polymorphic loci are also expression quantitative trait loci (eQTLs), DAR can lead to differences in gene expression which are not directly relevant to the primary research objectives. To mitigate DAR in both new and existing datsets, we introduce tadar, a Bioconductor package designed to facilitate transcriptome analysis by accounting for differential allelic representation. tadar implements a methodology that calculates a DAR metric at each polymorphic locus across the genome, which then serves as a predictive measure of a locus potential to cause eQTL-driven expression differences. This metric is then used to reduce eQTL noise in bulk RNA-Sequencing data.

bioinformatics↗

Iron Responsive Element (IRE)-mediated responses to iron dyshomeostasis in Alzheimer's disease

BackgroundIron trafficking and accumulation is associated with Alzheimers disease (AD) pathogenesis. However, the role of iron dyshomeostasis in early disease stages is uncertain. Currently, gene expression changes indicative of iron dyshomeostasis are not well characterized, making it difficult to explore these in existing datasets. ObjectiveTo identify sets of genes predicted to contain Iron Responsive Elements (IREs) and use these to explore possible iron dyshomeostasis-associated gene expression responses in AD. MethodsComprehensive sets of genes containing predicted IRE or IRE-like motifs in their 3 or 5 untranslated regions (UTRs) were identified in human, mouse, and zebrafish reference transcriptomes. Further analyses focusing on these genes were applied to a range of cultured cell, human, mouse, and zebrafish gene expression datasets. ResultsIRE gene sets are sufficiently sensitive to distinguish not only between iron overload and deficiency in cultured cells, but also between AD and other pathological brain conditions. Notably, changes in IRE transcript abundance are amongst the earliest observable changes in zebrafish familial AD (fAD)-like brains, preceding other AD-typical pathologies such as inflammatory changes. Unexpectedly, while some IREs in the 3 untranslated regions of transcripts show significantly increased stability under iron deficiency in line with current assumptions, many such transcripts instead display decreased stability, indicating that this is not a generalizable paradigm. ConclusionOur results reveal IRE gene expression changes as early markers of the pathogenic process in fAD and are consistent with iron dyshomeostasis as an important driver of this disease. Our work demonstrates how differences in the stability of IRE- containing transcripts can be used to explore and compare iron dyshomeostasis-associated gene expression responses across different species, tissues, and conditions.

bioinformatics↗