Course program
Unit 1 - Technologies for studying genetic variability and their applications (4 hours)
Methods for the molecular study of variants
Molecular analysis of gene mutations
Unit 2 - Methodologies and experimental approaches for studying epigenetic variations (4 hours)
Overview of methods for analyzing DNA methylation, histone modifications, ncRNA expression, ncRNA-protein binding, and ncRNA binding to chromatin
Unit 3 - Techniques for modifying the epigenome (2h)
Epigenetic enzyme inhibitors. RNA interference for epigenetic enzymes. CRISPR/Cas9 technology for inducing site-specific methylation
Unit 4 - “Omic” approaches to the study of genetic variability and gene expression (4h)
“Omic” technologies and systems biology. Genomics and genome sequencing
Functional genomics: transcriptomics, proteomics, epigenomics, and metabolomics
Unit 5 - Analysis of genetic variability in relation to drug susceptibility (2 hours)
Molecular basis of drug variability. Genomic analysis and pharmacogenetic testing. Epigenetic and non-coding aspects. Prospects and personalized medicine
Unit 6 - Genetic approaches to disease treatment (4 hours)
Replacement gene therapy. Genome editing (CRISPR-Cas9 and next-generation technologies). RNA-based therapies. Epigenetic therapies. CAR-T therapies and immune system engineering. Mitochondrial therapies.
Unit 7 - In-depth study of the methodologies covered (4 hours)
Simulations of theoretical questions, possible practical applications, and self-assessment tests to consolidate skills.
Books
1) Russell - Genetica. Un approccio molecolare- Pearson
2) Strachan e Lucassen - Genetica e Genomica nelle scienze mediche - Zanichelli
Teaching materials provided by lecturers