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Genetic screening identifies a SUMO protease dynamically maintaining centromeric chromatin.

Sreyoshi MitraDani L BodorAna F DavidIzma Abdul-ZaniJoão F MataBeate NeumannSabine ReitherChristian TischerLars E T Jansen
Published in: Nature communications (2020)
Centromeres are defined by a self-propagating chromatin structure based on stable inheritance of CENP-A containing nucleosomes. Here, we present a genetic screen coupled to pulse-chase labeling that allow us to identify proteins selectively involved in deposition of nascent CENP-A or in long-term transmission of chromatin-bound CENP-A. These include factors with known roles in DNA replication, repair, chromatin modification, and transcription, revealing a broad set of chromatin regulators that impact on CENP-A dynamics. We further identify the SUMO-protease SENP6 as a key factor, not only controlling CENP-A stability but virtually the entire centromere and kinetochore. Loss of SENP6 results in hyper-SUMOylation of CENP-C and CENP-I but not CENP-A itself. SENP6 activity is required throughout the cell cycle, suggesting that a dynamic SUMO cycle underlies a continuous surveillance of the centromere complex that in turn ensures stable transmission of CENP-A chromatin.
Keyphrases
  • genome wide
  • transcription factor
  • dna damage
  • gene expression
  • cell cycle
  • dna methylation
  • blood pressure
  • cell proliferation
  • public health
  • copy number
  • mitochondrial dna
  • oxidative stress
  • sensitive detection
  • single cell