Unknown

Dataset Information

0

Activation of DNA-PK by hairpinned DNA ends reveals a stepwise mechanism of kinase activation.


ABSTRACT: As its name implies, the DNA dependent protein kinase (DNA-PK) requires DNA double-stranded ends for enzymatic activation. Here, I demonstrate that hairpinned DNA ends are ineffective for activating the kinase toward many of its well-studied substrates (p53, XRCC4, XLF, HSP90). However, hairpinned DNA ends robustly stimulate certain DNA-PK autophosphorylations. Specifically, autophosphorylation sites within the ABCDE cluster are robustly phosphorylated when DNA-PK is activated by hairpinned DNA ends. Of note, phosphorylation of the ABCDE sites is requisite for activation of the Artemis nuclease that associates with DNA-PK to mediate hairpin opening. This finding suggests a multi-step mechanism of kinase activation. Finally, I find that all non-homologous end joining (NHEJ) defective cells (whether deficient in components of the DNA-PK complex or components of the ligase complex) are similarly deficient in joining DNA double-stranded breaks (DSBs) with hairpinned termini.

SUBMITTER: Meek K 

PROVIDER: S-EPMC7498359 | biostudies-literature | 2020 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications

Activation of DNA-PK by hairpinned DNA ends reveals a stepwise mechanism of kinase activation.

Meek Katheryn K  

Nucleic acids research 20200901 16


As its name implies, the DNA dependent protein kinase (DNA-PK) requires DNA double-stranded ends for enzymatic activation. Here, I demonstrate that hairpinned DNA ends are ineffective for activating the kinase toward many of its well-studied substrates (p53, XRCC4, XLF, HSP90). However, hairpinned DNA ends robustly stimulate certain DNA-PK autophosphorylations. Specifically, autophosphorylation sites within the ABCDE cluster are robustly phosphorylated when DNA-PK is activated by hairpinned DNA  ...[more]

Similar Datasets

| S-EPMC2876953 | biostudies-literature
| S-EPMC8992387 | biostudies-literature
| S-EPMC6664182 | biostudies-literature
| S-EPMC7482155 | biostudies-literature
| S-EPMC2435132 | biostudies-literature
| S-EPMC6414200 | biostudies-literature
| S-EPMC2475626 | biostudies-literature
| S-EPMC3789764 | biostudies-literature
| S-EPMC6755157 | biostudies-other
2023-07-05 | GSE235389 | GEO