Institute of Molecular Biology (IMB)
Roopesh Anand Joan Barau Petra Beli Claudia Keller Valsecchi René Ketting Anton Khmelinskii Julian König Nard Kubben Katja Luck Christof Niehrs Jan Padeken Stamatis Papathanasiou Katharina Papsdorf Sandra Schick Helle Ulrich Siyao Wang Sina WittmannChromatin regulation in health and disease
Genomic DNA is highly compacted into chromatin in order to fit into the nucleus of a cell. This packaging provides a regulatory layer for DNA accessibility and therefore all DNA-dependent processes, such as transcription, DNA repair or replication. ATP-dependent chromatin remodelers can modulate chromatin accessibility by moving or evicting nucleosomes. My research focuses on one particular class of chromatin remodelers known as BAF complexes, which are very large multi-protein complexes containing many subunits. Mutations in genes encoding BAF complex proteins occur in more than 20% of all human cancers and developmental diseases. In my research, I use a combination of genomics, proteomics, molecular biology, screening and imaging approaches to dissect the functions of individual BAF subunits in cancer and developmental disease.
Positions held
- Since 2021: Junior Faculty Member, Max Planck Graduate Center (MPGC), Mainz
- Since 2020: Group Leader, Institute of Molecular Biology (IMB), Mainz
- 2016 - 2020: Postdoctoral Researcher, CeMM, Vienna
Education
- 2016: Dr. rer. nat. in Molecular Biology, Institute of Molecular Biology (IMB), Mainz
- 2012: Diploma in Biology, Johannes Gutenberg University (JGU), Mainz
- 2012: Master in Biomedicine, Johannes Gutenberg University (JGU), Mainz
- 2008: Bachelor in Molecular Biology, Johannes Gutenberg University (JGU), Mainz
Selected publications by Sandra Schick
Schick S*, Grosche S*, Kohl KE*, Drpic D, Jaeger MG, Marella NC, Imrichova H, Lin JMG, Hofstätter G, Schuster M, Rendeiro AF, Koren A, Petronczki M, Bock C, Müller AC, Winter GE and Kubicek S (2021) Acute BAF perturbation causes immediate changes in chromatin accessibility. Nat Genet, 53:269–278 (*indicates joint contribution) Link
Varga J, Kube M, Luck K and Schick S (2021) The BAF chromatin remodeling complexes: structure, function, and synthetic lethalities. Biochem Soc Trans, 49:1489–1503 Link
Schick S, Rendeiro AF, Runggatscher K, Ringler A, Boidol B, Hinkel M, Májek P, Vulliard L, Penz T, Parapatics K, Schmidl C, Menche J, Boehmelt G, Petronczki M, Müller AC, Bock C and Kubicek S (2019) Systematic characterization of BAF mutations provides insights into intracomplex synthetic lethalities in human cancers. Nat Genet 51:1399-1410 Link
Sdelci S., Rendeiro AF, Rathert P, You W, Lin JG, Ringler A, Hofstätter G, Moll HP, Gürtl B, Farlik M, Schick S, Klepsch F, Oldach M, Buphamalai P, Schischlik F, Májek P, Parapatics K, Schmidl C, Schuster M, Penz T, Buckley DL, Hudecz O, Imre R, Wang SY, Maric HM, Kralovics R, Bennett KL, Müller AC, Mechtler K, Menche J, Bradner JE, Winter GE, Klavins K, Casanova E, Bock C, Zuber J and Kubicek S (2019) MTHFD1 interaction with BRD4 links folate metabolism to transcriptional regulation. Nat Genet 51:990-998 Link
Thakurela S*, Tiwari N*, Schick S, Garding A, Ivanek R, Berninger B and Tiwari VK (2016) Mapping gene regulatory circuitry of Pax6 during neurogenesis. Cell Discov, 2:15045 (*indicates joint contribution) Link
Schick S, Becker K, Thakurela S, Fournier D, Hampel MH, Legewie S and Tiwari VK (2016) Identifying novel transcriptional regularors with circadian expression. Mol Cell Biol, 36:545–558 Link
Schick S*, Fournier D*, Thakurela S, Sahu SK, Garding A and Tiwari VK (2015) Dynamics of chromatin accessibility and epigenetic state in response to UV damage. J Cell Sci, 128:4380–4394 (*indicates joint contribution) Link