Mechanisms for Microcephaly, Cancer and Autoinflammation Image Professor Andrew Jackson FRS Research in a Nutshell This programme identifies genes causing inherited disorders of the brain. We study how these genes function, using cells and model organisms.Aicardi-Goutières syndrome is a genetic condition in which faults in genes encoding enzymes called nucleases mimic viral infection of the brain. These nucleases may normally clean up naturally produced ‘waste’ DNA and RNA. Failure of this process leads to the body mounting an immune reaction against itself. This immune response mechanism is relevant to common autoimmune diseases such as lupus. So, we are studying these nucleases to understand their normal roles in cells and to establish what happens when these enzymes fail.From studying one of these nucleases, we have found that ribonucleotides, the building blocks of RNA, are also present in DNA. They can be harmful causing damage to the genome and can lead to mutations in cancers. The signature of such mutations may be useful in future in tailoring cancer therapies.We also discover genes that cause primordial dwarfism, conditions with extreme growth failure of the brain and body. Such individuals are the 'smallest people in the world'. These disorders are due to fewer cells being made during development, leading to a smaller person. Identifying primordial dwarfism genes helps diagnose and manage these rare conditions. It also gives insights into how the body regulates growth, perhaps shedding light into why humans are bigger than mice and how our brains evolved to be so large.Research Programme Image PeopleProfessor Andrew Jackson FRSGroup LeaderKamila MusialikResearch TechnicianAndrea RobertsonSenior Research Technician and Area SupervisorDiana Rios SzwedPostdoctoral ResearcherPaula CarrollResearch TechnicianColin StokPostdoctoral ResearcherMaggie MacDonaldResearch CoordinatorMartin ReijnsSenior Postdoctoral ResearcherLukas Tamayo OrregoPostdoctoral ResearcherDan SarniPostdoctoral ResearcherCarol-Anne MartinPostdoctoral ResearcherNic RobertsonClinical Research Fellow, CSO fellowshipXiong WengPostdoctoral ResearcherZicheng Yu (YC)PhD Student (with Professor Martin Taylor)Maarten van den AnckerPhD Student Zofia PukaloPhD Student (with Professor Jeyaprakash Arulanandam)ContactAndrew.Jackson@ed.ac.ukTop PublicationsIn silico protein interaction screening uncovers DONSON's role in replication initiation. Lim et al, Science 2023.Signatures of TOP1 transcription-associated mutagenesis in cancer and germline. Reijns et al, Nature 2022.Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of polycomb-regulated regions. Heyn et al, Nature Genetics 2019.CRISPR screens identify genomic ribonucleotides as a source of PARP-trapping lesions. Zimmermann et al, Nature 2019.cGAS surveillance of micronuclei links genome instability to innate immunity. Mackenzie et al, Nature 2017.CollaborationsProfessor Martin Taylor, MRC HGU, University of EdinburghProfessor Yanick Crow, MRC HGU, University of EdinburghDr Duncan Sproul, MRC HGU, University of EdinburghDr Tom Deegan, MRC HGU, University of EdinburghProfessor Nick Gilbert, MRC HGU, University of EdinburghProfessor Javier Caceres, MRC HGU, University of EdinburghDr Andrew Wood, MRC HGU, University of EdinburghDr Tamir Chandra, MRC HGU, University of EdinburghDr Joe Marsh, MRC HGU, University of EdinburghDr Ailith Ewing, MRC HGU, University of EdinburghDr Luke Boulter, MRC HGU, University of EdinburghProfessor Neil Henderson, MRC HGU (affiliate), CIR, University of EdinburghProfessor David Hunt, DRI, University of EdinburghProfessor Elaine Dzierzak, QMRI, University of EdinburghProfessor Jeyaprakash Arulanandam, Wellcome Centre for Cell Biology, University of EdinburghProfessor Grant Stewart, University of BirminghamProfessor Dan Durocher, University of TorontoProfessor Ian Hickson, University of CopenhagenProfessor Simon Boulton, The Francis Crick Institute, LondonProfessor Johannes Walter, Harvard Medical School, BostonProfessor Jan Rehwinkel, WIMM, University of OxfordProfessor Tuncay Baubec, Utrecht UniveristyProfessor Kamil Kranc, Queen Mary University, LondonProfessor Tatjana Stankovic, University of BirminghamDr Mike Bober, Nemours Children's Health, DelawareDr Carol Wise, University of Texas Southwestern Medical Center, DallasProfessor Bernd Wollnik, University of GottingenProfessor Valerie Cormier-Daire, ParisWalking with Giants Foundation, UKPotentials Foundation, USAPartners and FundersMedical Research CouncilEuropean Research CouncilEMBOScientific ThemesMicrocephaly, Aicardi-Goutieres syndrome, Ribonuclease H2, genome stability, inflammation, cancer This article was published on 2024-09-23