Evidence map›Paper›PMID 42079088›Full record

ArticlebioRxiv : the preprint server for biology2026

Long-lived mammals contain more phosphorylation sites in the SIRT6 C-terminus that enhance PARP1 interaction and resistance to oxidative stress.

Jonathan Gigas, Michael E Meadow, Jing Guo, Catherine Lan, Eric Hillpot, John C Martinez, Gregory Tombline, Philip Bellomio, Valeria Rivera Almodovar, Kevin A Welle and 6 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Jonathan GigasDepartment of Biology, University of Rochester, NY, 14627, USA.ORCID 0000-0002-0458-3181
Michael E MeadowDepartment of Biology, University of Rochester, NY, 14627, USA.
Jing GuoDepartment of Biology, University of Rochester, NY, 14627, USA.
Catherine LanDepartment of Biology, University of Rochester, NY, 14627, USA.
Eric HillpotDepartment of Biology, University of Rochester, NY, 14627, USA.
John C MartinezDepartment of Biology, University of Rochester, NY, 14627, USA.
Gregory TomblineDepartment of Biology, University of Rochester, NY, 14627, USA.
Philip BellomioDepartment of Biology, University of Rochester, NY, 14627, USA.
Valeria Rivera AlmodovarDepartment of Biology, University of Rochester, NY, 14627, USA.
Kevin A WelleUniversity of Rochester Mass Spectrometry Resource Laboratory, NY, 14627, USA.
Kyle SwovickUniversity of Rochester Mass Spectrometry Resource Laboratory, NY, 14627, USA.
Jennifer R HryhorenkoUniversity of Rochester Mass Spectrometry Resource Laboratory, NY, 14627, USA.
Julia AblaevaDepartment of Biology, University of Rochester, NY, 14627, USA.
Sina GhaemmaghamiDepartment of Biology, University of Rochester, NY, 14627, USA.
Andrei SeluanovDepartment of Biology, University of Rochester, NY, 14627, USA.
Vera GorbunovaDepartment of Biology, University of Rochester, NY, 14627, USA.

Funding

The role of hyaluronan in longevity and cancer resistance of longest-lived rodentP01AG047200 · NIA · UNIVERSITY OF ROCHESTER · PI Vadim N. Gladyshev · 2014 to 2026
$36.9M
The role of SIRT6 posttranslational modifications in aging and genome stability. Supplement: Testing SIRT6 activators as potential Alzheimer's disease therapy.R01AG027237 · NIA · UNIVERSITY OF ROCHESTER · PI Vera Gorbunova · 2006 to 2026
$6.2M
The prevalence and mechanism of selectivity in basal autophagyR35GM119502 · NIGMS · UNIVERSITY OF ROCHESTER · PI SINA GHAEMMAGHAMI · 2016 to 2026
$5.9M
Orbitrap Fusion Lumos Mass Spectrometer for UR Proteomics ResearchS10OD025242 · OD · UNIVERSITY OF ROCHESTER · PI GHAEMMAGHAMI, SINA · 2018 to 2018
$1.1M
NIA NIH HHS P01 AG047200NIA NIH HHS R01 AG027237NIGMS NIH HHS R35 GM119502NIH HHS S10 OD025242
6 · The paper itself

Abstract

Sirtuin 6 (SIRT6) is a protein deacetylase and ribosyltransferase that is a vital hub for maintaining epigenetic homeostasis, regulating the transcriptome, and repairing DNA double stranded breaks (DSBs). Comprehensive proteomic profiling of the SIRT6 post-translational landscape, however, remains elusive. The SIRT6 C-terminal domain contains multiple phosphorylation sites. We find that the presence and use of these sites is strongly correlated with maximum lifespan across mammals. Subsequent biochemical and

Indexed as

BiochemistryBiological SciencesComparative BiologyLongevityPhosphorylationSIRT6Stress Resistance

Identifiers

PMID42079088
PMCPMC13131647

What OpenQuestion holds

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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.