Evidence map›Paper›PMID 25756610›Full record

ArticleeLife2015

DNA damage shifts circadian clock time via Hausp-dependent Cry1 stabilization.

Stephanie J Papp, Anne-Laure Huber, Sabine D Jordan, Anna Kriebs, Madelena Nguyen, James J Moresco, John R Yates, Katja A Lamia

Open access · goldAbstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
16.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

76 citing papers in PubMed, 123 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Targeting Cryptochromes in Chronic Diseases.Cell biology international · 2025
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. The Influence of Circadian Rhythms on DNA Damage Repair in Skin Photoaging.International journal of molecular sciences · 2024
    Review
  13. Circadian rhythm disruption and endocrine-related tumors.World journal of clinical oncology · 2024
    Review
  14. Review
  15. Review
  16. A PDZ scaffolding/CaM-mediated pathway in Cryptochrome signaling.Protein science : a publication of the Protein Society · 2024
    Article
  17. c-Jun N-terminal kinase signaling in aging.Frontiers in aging neuroscience · 2024
    Review
  18. Review
  19. Article
  20. Article

16 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Stephanie J PappDepartment of Chemical Physiology, Scripps Research Institute, La Jolla, United States.
Anne-Laure HuberDepartment of Chemical Physiology, Scripps Research Institute, La Jolla, United States.
Sabine D JordanDepartment of Chemical Physiology, Scripps Research Institute, La Jolla, United States.
Anna KriebsDepartment of Chemical Physiology, Scripps Research Institute, La Jolla, United States.
Madelena NguyenDepartment of Chemical Physiology, Scripps Research Institute, La Jolla, United States.
James J MorescoDepartment of Chemical Physiology, Scripps Research Institute, La Jolla, United States.
John R YatesDepartment of Chemical Physiology, Scripps Research Institute, La Jolla, United States.
Katja A LamiaDepartment of Chemical Physiology, Scripps Research Institute, La Jolla, United States.
Scripps Research Institute · US

Funding

TrainingP41GM103533 · NIGMS · UNIVERSITY OF WASHINGTON · PI MACCOSS, MICHAEL · 2012 to 2021
$20.7M
Genetic Regulation of the Response to Dietary RestrictionR01AG027463 · NIA · UNIVERSITY OF CALIFORNIA BERKELEY · PI DILLIN, ANDREW G · 2008 to 2012
$2.4M
Circadian molecular regulation of the xenobiotic responseR01DK097164 · NIDDK · SCRIPPS RESEARCH INSTITUTE, THE · PI LAMIA, KATJA A · 2013 to 2017
$2.1M
Circadian Repressors Cry1 and Cry2 Modulate Nuclear Hormone Receptor FunctionK01DK090188 · NIDDK · SCRIPPS RESEARCH INSTITUTE, THE · PI LAMIA, KATJA A · 2011 to 2013
$446k
NIA NIH HHS R01 AG027463NIDDK NIH HHS K01 DK090188NIDDK NIH HHS R01 DK097164NIGMS NIH HHS P41 GM103533
6 · The paper itself

Abstract

The circadian transcriptional repressors cryptochrome 1 (Cry1) and 2 (Cry2) evolved from photolyases, bacterial light-activated DNA repair enzymes. In this study, we report that while they have lost DNA repair activity, Cry1/2 adapted to protect genomic integrity by responding to DNA damage through posttranslational modification and coordinating the downstream transcriptional response. We demonstrate that genotoxic stress stimulates Cry1 phosphorylation and its deubiquitination by Herpes virus associated ubiquitin-specific protease (Hausp, a.k.a Usp7), stabilizing Cry1 and shifting circadian clock time. DNA damage also increases Cry2 interaction with Fbxl3, destabilizing Cry2. Thus, genotoxic stress increases the Cry1/Cry2 ratio, suggesting distinct functions for Cry1 and Cry2 following DNA damage. Indeed, the transcriptional response to genotoxic stress is enhanced in Cry1-/- and blunted in Cry2-/- cells. Furthermore, Cry2-/- cells accumulate damaged DNA. These results suggest that Cry1 and Cry2, which evolved from DNA repair enzymes, protect genomic integrity via coordinated transcriptional regulation.

Indexed as

DNA DamageAnimalsCell LineCircadian ClocksCryptochromesMicePhosphorylationProtein BindingProtein StabilityTranscription, GeneticUbiquitin-Specific Peptidase 7Ubiquitin-Specific ProteasesCry1 protein, mouseCryptochromesUbiquitin-Specific Peptidase 7Ubiquitin-Specific ProteasesUsp7 protein, mousebiochemistrycircadian rhythmcryptochromeDNA damageHauspmouseneurosciencephosphorylationubiquitin

Identifiers

PMID25756610
PMCPMC4352707
OpenAlexW1974696079

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.