Subarea 4: Cell Dynamics and Molecular Damages in Aging
The research focus of Subarea 4 is on studying damages of macromolecules (proteins, nucleic acids) and determining the structure-function relationship of biomolecules relevant to damage and damage repair processes and responses to molecular damage that might lead to aging and aging-associated pathologies.
The studies are focused on the following research areas: DNA replication, DNA damage responses (DDR), stress responses, metabolic stresses, protein trafficking and protein damages.
The research is defined by four focus areas:
- DNA damage response in tissue homeostasis and neuropathies,
- Quality control in the endoplasmic reticulum for secretory pathway in aging processes,
- Intrinsic and extrinsic factors implicated in cellular decline during aging, and
- DNA replication and genomic integrity preventing premature aging and diseases.
Research focus of Subarea 4.
The accumulation of damaged macromolecules or subcellular organelles is associated with dysfunction of a cell, which contributes to tissue & organ failure. DNA damage, genomic instability, protein misfolding or defects in toxic protein degradation can compromise cell functionality. Alterations of mitochondrial DNA and protein complexes affect cellular metabolism, which will have a general impact on cell integrity.
Publications
(since 2016)
2021
- Butyrate and Metformin Affect Energy Metabolism Independently of the Metabolic Phenotype in the Tumor Therapy Model.
Meyer FB, Marx C, Spangel SB, Thierbach R
Biomolecules 2021, 11(12), 1831 - Silicon-rhodamine isothiocyanate for fluorescent labelling.
Nasufović V, Then P, Dröge F, Duong M, Kaether C, Dietzek B, Heintzmann R, Arndt HD
Org Biomol Chem 2021, 19(3), 574-8 - The LIM domain protein nTRIP6 modulates the dynamics of myogenic differentiation.
Norizadeh Abbariki T, Gonda Z, Kemler D, Urbanek P, Wagner T, Litfin M, Wang ZQ, Herrlich P, Kassel O
Sci Rep 2021, 11(1), 12904 - Biogenesis of Iron-Sulfur Clusters and Their Role in DNA Metabolism.
Shi R, Hou W, Wang ZQ, Xu X
Front Cell Dev Biol 2021, 9, 735678 - COPII collar defines the boundary between ER and ER exit site and does not coat cargo containers
Shomron O, Nevo-Yassaf I, Aviad T, Yaffe Y, Erez Zahavi E, Dukhovny A, Perlson E, Brodsky I, Yeheskel A, Pasmanik-Chor M, Mironov A, Beznoussenko GV, Mironov AA, Sklan EH, Patterson GH, Yonemura Y, Sannai M, Kaether** C, Hirschberg** K
J Cell Biol 2021, 220(6), e201907224 ** co-corresponding authors - TRIP6 functions in brain ciliogenesis.
Shukla S, Haenold* R, Urbánek* P, Frappart L, Monajembashi S, Grigaravicius P, Nagel S, Min WK, Tapias A, Kassel O, Heuer H, Wang ZQ, Ploubidou** A, Herrlich** P
Nat Commun 2021, 12(1), 5887 * equal contribution, ** co-senior authors - Poly(ADP-ribose) regulation in cell cycle control and cancer therapy
Siniuk K
Dissertation 2021, Jena, Germany - HAT cofactor TRRAP modulates microtubule dynamics via SP1 signaling to prevent neurodegeneration.
Tapias* A, Lázaro* D, Yin* BK, Rasa SMM, Krepelova A, Kelmer Sacramento E, Grigaravicius P, Koch P, Kirkpatrick J, Ori A, Neri F, Wang ZQ
Elife 2021, 10, e61531 * equal contribution - Beyond HAT Adaptor: TRRAP Liaisons with Sp1-Mediated Transcription.
Yin BK, Wang ZQ
Int J Mol Sci 2021, 22(22)
