Evidence map›Paper›PMID 25849655›Full record

ArticleInternational journal of molecular sciences2015

The neuronal-specific SGK1.1 (SGK1_v2) kinase as a transcriptional modulator of BAG4, Brox, and PPP1CB genes expression.

Rebeca González-Fernández, Julio Ávila, María F Arteaga, Cecilia M Canessa, Pablo Martín-Vasallo

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 95% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. 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

5 authors at 3 institutions in 4 countries.

Rebeca González-FernándezLaboratorio de Biología del Desarrollo, UD de Bioquímica y Biología Molecular and Centro de Investigaciones Biomédicas de Canarias (CIBICAN), Universidad de La Laguna, Av Astrofísico Sánchez s/n, La Laguna, Tenerife 38201, Spain. refernan@ull.es.
Julio ÁvilaLaboratorio de Biología del Desarrollo, UD de Bioquímica y Biología Molecular and Centro de Investigaciones Biomédicas de Canarias (CIBICAN), Universidad de La Laguna, Av Astrofísico Sánchez s/n, La Laguna, Tenerife 38201, Spain. javila@ull.es.
María F ArteagaDepartment of Cellular and Molecular Physiology, Yale University, 333 Cedar Street, New Haven, CT 06510, USA. marifrancis.arteaga@gmail.com.
Cecilia M CanessaDepartment of Cellular and Molecular Physiology, Yale University, 333 Cedar Street, New Haven, CT 06510, USA. cecilia.canessa@yale.edu.
Pablo Martín-VasalloLaboratorio de Biología del Desarrollo, UD de Bioquímica y Biología Molecular and Centro de Investigaciones Biomédicas de Canarias (CIBICAN), Universidad de La Laguna, Av Astrofísico Sánchez s/n, La Laguna, Tenerife 38201, Spain. pmartin@ull.es.
Universidad de La Laguna · ESUniversity of Münster · DEYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Serum- and Glucocorticoid-induced Kinase 1, SGK1, exhibits a broad range of cellular functions that include regulation of the number of ion channels in plasma membrane and modulation of signaling pathways of cell survival. This diversity of functions is made possible by various regulatory processes acting upon the SGK1 gene, giving rise to various isoforms: SGK1_v1-5, each with distinct properties and distinct aminotermini that serve to target proteins to different subcellular compartments. Among cellular effects of SGK1 expression is to indirectly modulate gene transcription by phosphorylating transcriptional factors of the FOXO family. Here we examined if SGK1.1 (SGK1_v2; NM_001143676), which associates primarily to the plasma membrane, is also able to regulate gene expression. Using a differential gene expression approach we identified six genes upregulated by SGK1.1 in HeLa cells. Further analysis of transcript and protein levels validated two genes: BCL2-associated athanogene 4 (BAG-4) and Brox. The results indicate that SGK1.1 regulates gene transcription upon a different set of genes some of which participate in cell survival pathways (BAG-4) and others in intracellular vesicular traffic (Brox).

Indexed as

Adaptor Proteins, Signal TransducingCell Line, TumorCell MembraneEndosomal Sorting Complexes Required for TransportForkhead Transcription FactorsGene ExpressionHeLa CellsHumansImmediate-Early ProteinsProtein Phosphatase 1Protein Serine-Threonine KinasesSerum-Glucocorticoid Regulated KinasesSignal TransductionTranscription FactorsTranscription, GeneticUp-RegulationAdaptor Proteins, Signal TransducingBAG4 protein, humanBROX protein, humanEndosomal Sorting Complexes Required for TransportForkhead Transcription FactorsImmediate-Early ProteinsPPP1CB protein, humanProtein Phosphatase 1Protein Serine-Threonine KinasesSerum-Glucocorticoid Regulated KinasesTranscription Factors

Identifiers

PMID25849655
PMCPMC4425028
OpenAlexW2076869840

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.