Evidence map›Paper›PMID 21695158›Full record

ArticlePloS one2011

Regulation of rDNA transcription by proto-oncogene PELP1.

Vijay K Gonugunta, Binoj C Nair, Rajib Rajhans, Gangadhara R Sareddy, Sujit S Nair, Ratna K Vadlamudi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  12. Minireview: Deciphering the Cellular Functions of PELP1.Molecular endocrinology (Baltimore, Md.) · 2015
    Review
  13. Article
  14. Article
  15. Article
  16. PELP1: a review of PELP1 interactions, signaling, and biology.Molecular and cellular endocrinology · 2014
    Review
  17. Article
  18. Article
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Vijay K GonuguntaDepartment of Obstetrics and Gynecology, and Cancer Therapy and Research Center, University of Texas Health Science Center, San Antonio, Texas, United States of America.
Binoj C Nair
Rajib Rajhans
Gangadhara R Sareddy
Sujit S Nair
Ratna K Vadlamudi
The University of Texas Health Science Center at San Antonio · US

Funding

PELP1, a Novel Regulator of Estrogen ReceptorR01CA095681 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI VADLAMUDI, RATNA K · 2003 to 2013
$2.5M
NCI NIH HHS CA0095681NCI NIH HHS R01 CA095681
6 · The paper itself

Abstract

backgroundProline-, glutamic acid-, and leucine-rich protein (PELP1) is a novel nuclear receptor coregulator with a multitude of functions. PELP1 serves as a scaffolding protein that couples various signaling complexes with nuclear receptors and participates as a transcriptional coregulator. Recent data suggest that PELP1 expression is deregulated in hormonal cancers, and that PELP1 functions as a proto-oncogene; however, the mechanism by which PELP1 promotes oncogenesis remains elusive. METHODOLOGY/PRINCIPAL

findingsUsing pharmacological inhibitors, confocal microscopy and biochemical assays, we demonstrated that PELP1 is localized in the nucleolus and that PELP1 is associated with the active ribosomal RNA transcription. Cell synchronization studies showed that PELP1 nucleolar localization varies and the greatest amount of nucleolar localization was observed during S and G2 phases. Using pharmacological compounds and CDK site mutants of PELP1, we found that CDK's activity plays an important role on PELP1 nucleolar localization. Depletion of PELP1 by siRNA decreased the expression of pre-rRNA. Reporter gene assays using ribosomal DNA (pHrD) luc-reporter revealed that PELP1WT but not PELP1MT enhanced the expression of reporter. Deletion of nucleolar domains abolished PELP1-mediated activation of the pHrD reporter. ChIP analysis revealed that PELP1 is recruited to the promoter regions of rDNA and is needed for optimal transcription of ribosomal RNA. CONCLUSIONS/SIGNIFICANCE: Collectively, our results suggest that proto-oncogene PELP1 plays a vital role in rDNA transcription. PELP1 modulation of rRNA transcription, a key step in ribosomal biogenesis may have implications in PELP1-mediated oncogenic functions.

Indexed as

Transcription, GeneticActive Transport, Cell NucleusCell CycleCell NucleolusCo-Repressor ProteinsCyclin-Dependent KinasesDNA, RibosomalHEK293 CellsHeLa CellsHumansPhosphorylationPromoter Regions, GeneticProtein Structure, TertiaryProto-Oncogene MasProto-Oncogene ProteinsTranscription FactorsCo-Repressor ProteinsCyclin-Dependent KinasesDNA, RibosomalMAS1 protein, humanPELP1 protein, humanProto-Oncogene MasProto-Oncogene ProteinsTranscription Factors

Identifiers

PMID21695158
PMCPMC3113909
OpenAlexW2001981679

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.