miRNA dysregulation in embryo results in autism spectrum disorder
Minoo Rassoulzadegan· Université de Nice, INSERM-CNRS, France; Genome and Stem Cell Center, Erciyes University, Kayseri, Turkey
Thu, Jun 17 · 17:30 UTC
Seminars and recordings
Minoo Rassoulzadegan· Université de Nice, INSERM-CNRS, France; Genome and Stem Cell Center, Erciyes University, Kayseri, Turkey
Thu, Jun 17 · 17:30 UTC
Andre Fischer· University Medical Center Goettingen, DZNE Goettingen
Thu, Jun 17 · 16:45 UTC
The establishment of effective therapies for neurodegenerative and neuropsychiatric diseases is still challenging and one of the reasons is that especially for age-associated neurodegenerative diseases pathology accumulates long before there are any clinical signs of disease. Thus, patients are often only diagnosed at an already advanced state of molecular pathology, when causative therapies fail. Thus, there is an urgent need for molecular biomarkers that could detect individuals at risk for developing a CNS disease and stratify patients. I will address epigenetic processes such as histone-modifications and non-coding RNAs as potential approaches for patient stratification and therapeutic interaction, with a specific focus on RNA-therapies. Here, I plan to cover examples from our recent research on Alzheimer’s disease and Schizophrenia.
Stefan Stricker· Institute of Strem Cell Research, Helmholtz Zentrum Munich
Thu, Jun 17 · 16:00 UTC
Schahram Akbarian· Icahn School of Medicine at Mt. Sinai
Thu, Jun 17 · 15:00 UTC
Repeat-rich sequence blocks are considered major determinants for 3D folding and structural genome organization in the cell nucleus in all higher eukaryotes. Here, we discuss how megabase-scale chromatin domain and chromosomal compartment organization in adult mouse cerebral cortex is linked, in highly cell type-specific fashion, to multiple retrotransposon superfamilies which comprise the vast majority of mobile DNA elements in the murine genome. We show that neuronal megadomain architectures include an evolutionarily adaptive heterochromatic organization which, upon perturbation, unleashes proviruses from the Long Terminal Repeat (LTR) Endogenous Retrovirus family that exhibit strong tropism in mature neurons. Furthermore, we mapped, in the human brain, cell type-specific genomic integration patterns of the human pathogen and exogenous retrovirus, HIV, together with changes in genome organization and function of the HIV infected brain. Our work highlights the critical importance of chromosomal conformations and the ‘spatial genome’ for neuron- and glia-specific regulatory mechanisms and defenses aimed at exogenous and endogenous retrotransposons in the brain
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