Evidence map›Paper›PMID 31749682›Full record

ArticleFrontiers in molecular neuroscience2019

Nuclear Tau, p53 and Pin1 Regulate PARN-Mediated Deadenylation and Gene Expression.

Jorge Baquero, Sophia Varriano, Martha Ordonez, Pawel Kuczaj, Michael R Murphy, Gamage Aruggoda, Devon Lundine, Viktoriya Morozova, Ali Elhadi Makki, Alejandra Del C Alonso and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
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

11 authors at 3 institutions in 1 country.

Jorge BaqueroChemistry Department, Hunter College and Biochemistry Program, The Graduate Center, The City University of New York, New York, NY, United States.
Sophia VarrianoChemistry Department, Hunter College and Biochemistry Program, The Graduate Center, The City University of New York, New York, NY, United States.
Martha OrdonezChemistry Department, Hunter College and Biochemistry Program, The Graduate Center, The City University of New York, New York, NY, United States.
Pawel KuczajChemistry Department, Hunter College and Biochemistry Program, The Graduate Center, The City University of New York, New York, NY, United States.
Michael R MurphyChemistry Department, Hunter College and Biochemistry Program, The Graduate Center, The City University of New York, New York, NY, United States.
Gamage AruggodaChemistry Department, Hunter College and Biochemistry Program, The Graduate Center, The City University of New York, New York, NY, United States.
Devon LundineChemistry Department, Hunter College and Biochemistry Program, The Graduate Center, The City University of New York, New York, NY, United States.
Viktoriya MorozovaDepartment of Biology and Center for Developmental Neuroscience, College of Staten Island, Graduate Center, The City University of New York, Staten Island, NY, United States.
Ali Elhadi MakkiDepartment of Biology and Center for Developmental Neuroscience, College of Staten Island, Graduate Center, The City University of New York, Staten Island, NY, United States.
Alejandra Del C AlonsoDepartment of Biology and Center for Developmental Neuroscience, College of Staten Island, Graduate Center, The City University of New York, Staten Island, NY, United States.
Frida E KleimanChemistry Department, Hunter College and Biochemistry Program, The Graduate Center, The City University of New York, New York, NY, United States.
The Graduate Center, CUNY · USHunter College · USCity University of New York · US

Funding

RISE Program Hunter College Option IIIR25GM060665 · NIGMS · HUNTER COLLEGE · PI ORTIZ, BENJAMIN D.,, SERRANO, PETER A · 2000 to 2022
$22.8M
TUFCCC/HC Regional Comprehensive Cancer Health PartnershipU54CA221705 · NCI · TEMPLE UNIV OF THE COMMONWEALTH · PI Yin Tan · 2018 to 2026
$16.3M
TUFCCC/HC Regional Comprehensive Cancer Health PartnershipU54CA221704 · NCI · HUNTER COLLEGE · PI Joel Erblich, Jennifer S Ford · 2018 to 2026
$10.6M
Mechanism of tau pathological SpreadingR15AG058197 · NIA · COLLEGE OF STATEN ISLAND · PI ALONSO, ALEJANDRA DEL-C · 2018 to 2018
$450k
Role of the mRNA 3’ processing factor CstF-50 in regulating the BRCA1/BARD1 E3 ubiquitin ligase activity during the DNA damage responseR21CA204610 · NCI · HUNTER COLLEGE · PI KLEIMAN, FRIDA E · 2017 to 2018
$373k
Tau phosphorylation and neurodegenerationR15AG034524 · NIA · COLLEGE OF STATEN ISLAND · PI ALONSO, ALEJANDRA DEL-C · 2009 to 2009
$149k
NCI NIH HHS R21 CA204610NCI NIH HHS U54 CA221704NCI NIH HHS U54 CA221705NIA NIH HHS R15 AG034524NIA NIH HHS R15 AG058197NIGMS NIH HHS R25 GM060665
6 · The paper itself

Abstract

While nuclear tau plays a role in DNA damage response (DDR) and chromosome relaxation, the mechanisms behind these functions are not fully understood. Here, we show that tau forms complex(es) with factors involved in nuclear mRNA processing such as tumor suppressor p53 and poly(A)-specific ribonuclease (PARN) deadenylase. Tau induces PARN activity in different cellular models during DDR, and this activation is further increased by p53 and inhibited by tau phosphorylation at residues implicated in neurological disorders. Tau's binding factor Pin1, a mitotic regulator overexpressed in cancer and depleted in Alzheimer's disease (AD), also plays a role in the activation of nuclear deadenylation. Tau, Pin1 and PARN target the expression of mRNAs deregulated in AD and/or cancer. Our findings identify novel biological roles of tau and toxic effects of hyperphosphorylated-tau. We propose a model in which factors involved in cancer and AD regulate gene expression by interactions with the mRNA processing machinery, affecting the transcriptome and suggesting insights into alternative mechanisms for the initiation and/or developments of these diseases.

Indexed as

cellular DNA damagemRNA processingnuclear taup53Pin1

Identifiers

PMID31749682
PMCPMC6843027
OpenAlexW2980925175

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.