3 results
Protein-structure prediction can help distinguish competing gene models. Studies of two fungi and an apicoplast compare original and manually curated annotations, finding that structure-derived scores favour curated models when predictions differ in structured domains. These signals complement sequence-domain analysis but offer little help for uncertainty in potentially disordered regions. The presentation also examines Protenix-mini as a faster alternative retaining discriminatory power, complete-proteome scoring, and a NextFlow pipeline intended to make the workflow usable. It considers applications when transcriptomic evidence is limited and the remaining limitations of structure-based annotation.
Thu, Nov 19 · 10:00 UTC · Online
Josh Levendis examines how N6-methyladenosine RNA modification controls gene expression in Plasmodium falciparum. Nanopore direct RNA sequencing and GLORI-seq reveal enrichment near transcript ends. Inducible mislocalisation of methyltransferase depletes this modification and produces readthrough and chimeric transcripts, implicating methylation in correct polyadenylation and transcription termination. Stage-dependent modification of exons and retained introns may also regulate early termination during sexual development. Alex Harris investigates why protection from RTS,S malaria vaccination and seasonal chemoprevention declines despite annual boosters. Analyses of plasma from 1,929 West African children followed over four years assess antibody responses to different antigen regions and their variation with host factors, coinfections and micronutrients. The work examines declining booster responses and aims to inform strategies for durable vaccine protection.
Fri, Nov 20 · 02:00 UTC · Online
Interpreting human missense variants requires connecting genomic coordinates with protein sequences, structures and functional evidence. ProtVar integrates annotations and predictions from UniProt, Ensembl, PDBe, Open Targets and AlphaFoldDB, extending variant lookup to discovery across more than 500 million potential missense variants. This seminar demonstrates natural-language searches using diseases, pathways and drug responses, multi-criteria filtering, structural visualisation and data export. Participants will learn to prioritise variants, interpret their structural and functional effects, and retrieve data through web downloads or the REST API. The session serves geneticists, drug-discovery researchers and computational biologists; undergraduate molecular biology and genetics are recommended.
Thu, Dec 3 · 15:00 UTC · Online
Michelle M. Li examines how computational analyses can preserve the biological context of a proposed treatment, including cell type, disease state, genetic background and patient characteristics. She introduces Medea, an AI system that combines biological software, predictive models and literature retrieval while checking intermediate steps and reconciling evidence. The seminar presents evaluations involving cell-specific target selection, cancer-cell synthetic lethality and immunotherapy response. A separate yeast experiment tests predictions against previously unpublished measurements of gene-pair interactions under DNA-damaging treatments. The research addresses whether an agent can transfer useful evidence between contexts while recognizing when that transfer is unsupported. Reported comparisons cover predictive performance, computational failures and the ability to abstain. This recording retains the original seminar date.
Recorded
Ant colonies depend heavily on chemical communication, creating demanding problems for sensory gene regulation. This lecture examines the expansion of olfactory-receptor gene families and the mechanisms that select a receptor for each neuron. Comparisons with vertebrates illuminate how stochastic gene choices support organised sensory systems.
Recorded
This lecture examines genetic control of tail length using variation between deer-mouse populations and targeted experiments. It considers multiple quantitative-trait loci, the possible role of Hoxd13 expression and evidence from altered Hox13 activity. Vertebral development provides a case study of how changes in gene regulation can produce evolutionary changes in body form.
Recorded
This lecture compares two approaches to the evolution of mammalian tails. It critically examines the proposed role of altered Tbxt splicing in ape tail loss, including difficulties interpreting mouse experiments. It then introduces quantitative-genetic studies of deer mice in different habitats, where several loci contribute to variation in tail length.
Recorded
This lecture traces research on the mouse T locus and the Tbxt gene before examining a proposed mechanism of tail loss in apes. A repeated DNA insertion may alter splicing and protein production. The discussion asks how a small genetic change could affect development and generate a large, persistent evolutionary transformation.
Recorded
Tail development provides a case study for connecting genetic change to the evolution of anatomy. This lecture introduces relevant ideas from evolutionary developmental biology and RNA splicing, then considers variation in tail presence and length across mammals. It also examines what different experimental approaches can establish about DNA, form and function.
Recorded