Evidence map›Paper›PMID 18786246›Full record

ArticleBMC genomics2008

Identification of direct regulatory targets of the transcription factor Sox10 based on function and conservation.

Kyung Eun Lee, Seungyoon Nam, Eun-ah Cho, Ikjoo Seong, Jin-Kyung Limb, Sanghyuk Lee, Jaesang Kim

Abstract read
In one paragraph

Article in BMC genomics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Deletion ofBiomedicines · 2023
    Article
  3. A Novel Role for Oligodendrocyte Precursor Cells (OPCs) and Sox10 in Mediating Cellular and Behavioral Responses to Heroin.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
  4. SOX10 is over-expressed in bladder cancer and contributes to the malignant bladder cancer cell behaviors.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2017
    Article
  5. Article
  6. Sox10 expression in ovarian epithelial tumors is associated with poor overall survival.Virchows Archiv : an international journal of pathology · 2016
    Article
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  16. Uncovering the transcriptional circuitry in skeletal muscle regeneration.Mammalian genome : official journal of the International Mammalian Genome Society · 2011
    Article
  17. Sox proteins in melanocyte development and melanoma.Pigment cell & melanoma research · 2010
    Review
  18. Comparative analysis of MTF-1 binding sites between human and mouse.Mammalian genome : official journal of the International Mammalian Genome Society · 2010
    Article
  19. Article
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

7 authors.

Kyung Eun LeeDivision of Life and Pharmaceutical Sciences and the Center for Cell Signaling & Drug Discovery Research, Ewha Womans University, 11-1 Daehyun-dong, Seodaemun-gu, Seoul, 120-750, Korea. kamsi97@hanmail.net
Seungyoon Nam
Eun-ah Cho
Ikjoo Seong
Jin-Kyung Limb
Sanghyuk Lee
Jaesang Kim

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSox10, a member of the Sry-related HMG-Box gene family, is a critical transcription factor for several important cell lineages, most notably the neural crest stem cells and the derivative peripheral glial cells and melanocytes. Thus far, only a handful of direct target genes are known for this transcription factor limiting our understanding of the biological network it governs.

resultsWe describe identification of multiple direct regulatory target genes of Sox10 through a procedure based on function and conservation. By combining RNA interference technique and DNA microarray technology, we have identified a set of genes that show significant down-regulation upon introduction of Sox10 specific siRNA into Schwannoma cells. Subsequent comparative genomics analyses led to potential binding sites for Sox10 protein conserved across several mammalian species within the genomic region proximal to these genes. Multiple sites belonging to 4 different genes (proteolipid protein, Sox10, extracellular superoxide dismutase, and pleiotrophin) were shown to directly interact with Sox10 by chromatin immunoprecipitation assay. We further confirmed the direct regulation through the identified cis-element for one of the genes, extracellular superoxide dismutase, using electrophoretic mobility shift assay and reporter assay.

conclusionIn sum, the process of combining differential expression profiling and comparative genomics successfully led to further defining the role of Sox10, a critical transcription factor for the development of peripheral glia. Our strategy utilizing relatively accessible techniques and tools should be applicable to studying the function of other transcription factors.

Indexed as

AnimalsBinding SitesCell Line, TumorChromatin ImmunoprecipitationDNA-Binding ProteinsGene Expression RegulationGenomicsHigh Mobility Group ProteinsHumansNeurogliaOligonucleotide Array Sequence AnalysisRNA InterferenceSOXE Transcription FactorsTranscription FactorsDNA-Binding ProteinsHigh Mobility Group ProteinsSOX10 protein, humanSOXE Transcription FactorsTranscription Factors

Identifiers

PMID18786246
PMCPMC2556353

What OpenQuestion holds

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LicenceCC BY
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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.