Evidence map›Paper›PMID 23904271›Full record

ArticleMolecular biology of the cell2013

Functional activity of RLIM/Rnf12 is regulated by phosphorylation-dependent nucleocytoplasmic shuttling.

Baowei Jiao, Naoko Taniguchi-Ishigaki, Cenap Güngör, Marvin A Peters, Ya-Wen Chen, Sabine Riethdorf, Alexander Drung, Leanne G Ahronian, Jongdae Shin, Rachna Pagnis and 5 more

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

22 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  4. Roles of the Rlim-Rex1 axis during X chromosome inactivation in mice.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  15. Rlim/Rnf12, Rex1, and X Chromosome Inactivation.Frontiers in cell and developmental biology · 2019
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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

15 authors at 5 institutions in 5 countries.

Baowei JiaoProgram in Gene Function and Expression, University of Massachusetts Medical School, Worcester, MA 01605-2324 Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605-2324 Centre for Molecular Neurobiology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany Institute for Tumor Biology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Naoko Taniguchi-Ishigaki
Cenap Güngör
Marvin A Peters
Ya-Wen Chen
Sabine Riethdorf
Alexander Drung
Leanne G Ahronian
Jongdae Shin
Rachna Pagnis
Klaus Pantel
Taro Tachibana
Brian C Lewis
Steven A Johnsen
Ingolf Bach
University of Massachusetts Chan Medical School · USTU Dresden · DEUniversität Hamburg · DEUniversity Medical Center Hamburg-Eppendorf · DEInstitute of Neurobiology and Molecular Medicine · IT

Funding

PILOT AND FEASIBILITY PROGRAMP30DK032520 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CZECH, MICHAEL P · 1986 to 2010
$14.6M
Roles of LIM cofactors for regulating ERalpha during oncogenesis and developmentR01CA131158 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BACH, INGOLF M · 2008 to 2017
$3.3M
NCI NIH HHS R01 CA131158NCI NIH HHS R01CA131158NIDDK NIH HHS DK32520NIDDK NIH HHS P30 DK032520
6 · The paper itself

Abstract

The X-linked gene Rnf12 encodes the ubiquitin ligase really interesting new gene (RING) finger LIM domain-interacting protein (RLIM)/RING finger protein 12 (Rnf12), which serves as a major sex-specific epigenetic regulator of female mouse nurturing tissues. Early during embryogenesis, RLIM/Rnf12 expressed from the maternal allele is crucial for the development of extraembryonic trophoblast cells. In contrast, in mammary glands of pregnant and lactating adult females RLIM/Rnf12 expressed from the paternal allele functions as a critical survival factor for milk-producing alveolar cells. Although RLIM/Rnf12 is detected mostly in the nucleus, little is known about how and in which cellular compartment(s) RLIM/Rnf12 mediates its biological functions. Here we demonstrate that RLIM/Rnf12 protein shuttles between nucleus and cytoplasm and this is regulated by phosphorylation of serine S214 located within its nuclear localization sequence. We show that shuttling is important for RLIM to exert its biological functions, as alveolar cell survival activity is inhibited in cells expressing shuttling-deficient nuclear or cytoplasmic RLIM/Rnf12. Thus regulated nucleocytoplasmic shuttling of RLIM/Rnf12 coordinates cellular compartments during mammary alveolar cell survival.

Indexed as

Active Transport, Cell NucleusAnimalsCell NucleusCell SurvivalEmbryonic DevelopmentEpigenesis, GeneticFemaleHeLa CellsHumansLIM Domain ProteinsMammary Glands, AnimalMicePhosphorylationPregnancySex Determination ProcessesUbiquitin-Protein LigasesLIM Domain ProteinsRLIM protein, humanUbiquitin-Protein Ligases

Identifiers

PMID23904271
PMCPMC3784382
OpenAlexW2163364385

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.