Back

HIPK2-and IKKβ-dependent phosphorylation stabilizes TAp63α during the oocyte DNA damage response

Kumari, A.; P, K. K.; Mohanty, A.; S, A.; S, L. K.; E, A. K.; Athar, M.; Birajdar, P.; Kumar, A.; Y, S.; Sabnam, S.; Prasada Rao, H.

2026-04-21 cell biology
10.64898/2026.04.17.719163 bioRxiv
Show abstract

TAp63, a member of the p53 family, serves as a central quality control factor in oocytes, safeguarding genomic integrity during the prolonged dictyate arrest of meiosis. In healthy oocytes, TAp63 is maintained in an inactive dimeric state; upon DNA damage, it undergoes phosphorylation-dependent tetramerization, enabling transcriptional activation of pathways that determine oocyte fate. While the upstream activation cascade of TAp63 has been well characterized, the mechanisms that regulate its stability during the DNA damage response remain incompletely understood. Here, we identify the kinases HIPK2 and IKK{beta} as key regulators of TAp63 stability. We show that TAp63 interacts with both kinases and is phosphorylated at distinct residues, T452 by HIPK2 and S4/S12 by IKK{beta} in vitro and in vivo, in addition to previously described CHK2 and CK1-mediated phosphorylation. Functionally, these phosphorylation events do not primarily contribute to activation, but instead stabilize TAp63 by limiting MDM4-dependent ubiquitination and subsequent proteasomal degradation. Mechanistically, our data support a model in which CHK2 and CK1 initiate TAp63 phosphorylation, while HIPK2 and IKK{beta} act in a complementary manner to maintain protein stability during genotoxic stress. Disruption of HIPK2 or IKK{beta} activity reduces TAp63 stability, whereas their inhibition in vivo attenuates oocyte loss following DNA damage, resulting in increased preservation of the follicle pool. Importantly, these effects are observed across multiple systems, including mouse models and ex vivo goat ovary cultures, supporting an evolutionarily conserved role for this regulatory axis. Together, our findings uncover a previously unidentified layer of TAp63 regulation, in which phosphorylation not only contributes to its activation but also enhances protein stability, thereby fine-tuning oocyte responses to DNA damage. Our results further indicate that HIPK2 and IKK{beta}-mediated phosphorylation modulates oocyte survival under genotoxic stress, highlighting this pathway as a potential target for strategies aimed at limiting oocyte loss.

Matching journals

The top 5 journals account for 50% of the predicted probability mass.

1
Molecular Cell
308 papers in training set
Top 0.5%
18.1%
2
Developmental Cell
168 papers in training set
Top 1%
12.3%
3
Cell Reports
1338 papers in training set
Top 3%
9.8%
4
Journal of Cell Biology
333 papers in training set
Top 0.3%
8.9%
5
Current Biology
596 papers in training set
Top 3%
6.2%
50% of probability mass above
6
eLife
5422 papers in training set
Top 18%
4.7%
7
Proceedings of the National Academy of Sciences
2130 papers in training set
Top 18%
3.9%
8
Nature Cell Biology
99 papers in training set
Top 1%
3.5%
9
Nature Communications
4913 papers in training set
Top 41%
3.5%
10
EMBO reports
136 papers in training set
Top 1%
2.7%
11
PLOS Genetics
756 papers in training set
Top 7%
2.3%
12
Nucleic Acids Research
1128 papers in training set
Top 9%
2.0%
13
Science Advances
1098 papers in training set
Top 16%
1.7%
14
Molecular Biology of the Cell
272 papers in training set
Top 1%
1.6%
15
The EMBO Journal
267 papers in training set
Top 3%
1.3%
16
PLOS Biology
408 papers in training set
Top 14%
1.2%
17
Blood
67 papers in training set
Top 1%
1.1%
18
JCI Insight
241 papers in training set
Top 6%
0.9%
19
EMBO Reports
88 papers in training set
Top 0.6%
0.8%
20
Journal of Cell Science
353 papers in training set
Top 2%
0.8%
21
Cell Systems
167 papers in training set
Top 12%
0.8%
22
Cell Chemical Biology
81 papers in training set
Top 4%
0.7%
23
iScience
1063 papers in training set
Top 36%
0.7%
24
Nature Structural & Molecular Biology
218 papers in training set
Top 6%
0.6%