Impact of Tau Overexpression on DNA Replication Dynamics in Centromeres of Human Neural Progenitor Cells. Balzano et al
Description
Aging somatic cells are characterized by specific chromosome aneuploidy, particularly involving chromosomes Y (ChrY) and 21 (Chr21), which are associated with Alzheimer’s Disease (AD) pathology. This study investigates DNA replication within centromeric regions of these chromosomes using human neural progenitor cells engineered to overexpress either wild-type (wt) or pseudo-hyper-phosphorylated (php) Tau protein. We developed a method to analyze replication dynamics in centromeric DNA. Our findings reveal that replication origins and fork pausing events are mainly located within α-satellite sequences of ChrY and Chr21, where wt and php Tau distinctly modulate origin activation and initiation. Mass spectrometry analysis on immunoprecipitated Tau identified nuclear interactors of Tau, particularly in its php form, which might directly influence chromatin architecture and gene expression. These studies provide critical insights into the molecular mechanisms of aneuploidy in tauopathies.
Files
Steps to reproduce
For detailed technical information on Chr21 SMARD, please refer to the uploaded file titled "SMARD protocols". The file also includes protocols for ChrY and rDNA.
Institutions
- Yeshiva University Albert Einstein College of Medicine