SEEK ID: https://seek-for2800.de/people/10
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Germany
ORCID: Not specified
Joined: 10th Nov 2021
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Our Research Unit addresses an important question on the origin of chromosome instability (CIN), which causes structural as well as numerical chromosome aberrations. Importantly, CIN and increased levels of chromosome aberrations are closely associated with many human diseases including cancer, neurodegenerative diseases and age-related syndromes and can act as key drivers for disease development and progression. An important condition that causes structural chromosome instability (S-CIN) leading ...
Projects: SP-3: A statistical modeling approach to identify common triggers for replication stress and mitotic chromosome missegregation, SP-1: Deciphering signaling pathways that promote accurate chromosome segregation after replication stress, SP-2: Molecular mechanisms of replication stress-induced mitotic chromosome missegregation, SP-4: Centrosome integrity as a determinant of replication stress and mitotic dysfunction, SP-5: Impaired chromosome integrity caused by mutations in members of the BTR complex, SP-6: Proteomics of mitotic inter sister chromatid junctions, SP-8: The causes of replication stress in response to whole chromosomal aneuploidy, SP-Z: NGS-based approaches for systematic analysis of genomic and chromosome instability Bernd Wollnik, Göttingen, SP9: Mutual impact of replication origin firing regulation and mitotic chromosome segregation
Web page: https://for2800.de/
Replication stress is a key driver of genomic instability giving rise to human disease, for instance cancer or developmental disorders. It is caused by a variety of defects such as lesions blocking replication (e.g. DNA interstrand crosslinks) or processes that lead to the exhaustion of DNA precursors. This generates under-replicated DNA and replication intermediates that can be rescued by repair processes requiring homologous recombination between sister chromatids. Often, cells exposed to ...
Programme: FOR2800
Public web page: https://for2800.de/cases/sub-project-6-proteomics-of-mitotic-inter-sister-chromatid-junctions/
Organisms: Not specified
CHIP-MS was performed with HeLa cells carrying a bacterial artifical chromosome for the expression of GFP-tagged PICH under it's endogenous promotor. Cells were treated with drugs to induce different types of ultra-fine bridges (UFBs). Treatments included: a) 24h exposure to 0.1 uM Aphidicolin, b) 24 hours exposure to 120 ng/ml mitomycin C, c) 6.5 hours incubation in 0.05 ug/ml nocodazol followed by a release into 0.1 uM ICRF-193 topoisomerase inhibitor.
Submitter: Markus Räschle
Assay type: Experimental Assay Type
Technology type: Technology Type
Investigation: Identification of factors involved in UFB resol...
Study: 1 hidden item
Abstract (Expand)
Authors: Ipek Ilgin Gönenc, Alexander Wolff, Markus Räschle, Bernd Wollnik
Date Published: 1st Oct 2021
Publication Type: Journal
DOI: 10.1101/2021.10.01.462717
Citation:
Abstract (Expand)
Authors: N. K. Chunduri, P. Menges, X. Zhang, A. Wieland, V. L. Gotsmann, B. R. Mardin, C. Buccitelli, J. O. Korbel, F. Willmund, M. Kschischo, M. Raeschle, Z. Storchova
Date Published: 22nd Sep 2021
Publication Type: Journal
PubMed ID: 34552071
Citation: Nat Commun. 2021 Sep 22;12(1):5576. doi: 10.1038/s41467-021-25288-x.
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