Inviting an author to review:
Find an author and click ‘Invite to review selected article’ near their name.
Search for authorsSearch for similar articles
26
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      DAX1 regulatory networks unveil conserved and potentially new functions.

      1 , , , ,
      Gene
      Elsevier BV
      18S, 18S ribosomal RNA, ACTB, ACTH, ANOVA, Arβ, CAH, CAM, CILP, CYP, Ca(2+)-calmodulin, DAX1, DBD, DMSO, DNA-binding domain, Dosage-sensitive sex reversal in Adrenal Hypoplasia Congenita critical region on X chromosome, gene 1 , EF1α, ERα=ESR1, Erβ=ESR2, FSH, GO, Gene Ontology, Gene networks, GnRH, HPGA, HSD, IGF1, KCN, LH, MIS, MO, MS222, Müllerian inhibiting substance, N-(6-aminohexyl)-5- chloro-1-naphtalensulfonamide, Nr0B1, ORF, Osmoregulation, PKC, PRL, Pax, Promoter architecture, SCN, SF1, SHP=Nr0B2, SLC, StAR, Steroidogenesis, Steroidogenic acute regulatory protein, TFBS, TSS, Transcription binding sites, Transcription factor binding site, Tricaine methanesulfonate, W7, adrenocorticotrophic hormone, analysis of variance, androgen receptor beta, beta actin, cAMP, cartilage intermediate layer protein, congenital adrenal hypoplasia, cyclic adenosine monosphosphate, cytochrome P-450, dimethyl sulphoxide, elongation factor 1 alpha, follicle stimulating hormone, gonadotrophin releasing hormone, hydroxysteroid dehydrogenase, hypothalamic-pituitary-gonadal-adrenal axis, insulin-like growth factor I, luteinizing hormone, morpholino, oestrogen receptor alpha or 1, oestrogen receptor beta or 2, open reading frame, orphan nuclear receptor 0 B, paired box, potassium channel, prolactin, protein kinase C, qPCR, reverse-transcription quantitative polymerase chain reaction, runt-related transcription factor 2, runx 2, small heterodimer protein, sodium channel, solute carrier, steroidogenic factor 1, transcription start site

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          DAX1 is an orphan nuclear receptor with actions in mammalian sex determination, regulation of steroidogenesis, embryonic development and neural differentiation. Conserved patterns of DAX1 gene expression from mammals to fish have been taken to suggest conserved function. In the present study, the European sea bass, Dicentrarchus labrax, DAX1 promoter was isolated and its conserved features compared to other fish and mammalian DAX1 promoters in order to derive common regulators and functional gene networks. Fish and mammalian DAX1 promoters share common sets of transcription factor frameworks which were also present in the promoter region of another 127 genes. Pathway analysis clustered these into candidate gene networks associated with the fish and mammalian DAX1. The networks identified are concordant with described functions for DAX1 in embryogenesis, regulation of transcription, endocrine development and steroid production. Novel candidate gene network partners were also identified, which implicate DAX1 in ion homeostasis and transport, lipid transport and skeletal development. Experimental evidence is provided supporting roles for DAX1 in steroid signalling and osmoregulation in fish. These results highlight the usefulness of the in silico comparative approach to analyse gene regulation for hypothesis generation. Conserved promoter architecture can be used also to predict potentially new gene functions. The approach reported can be applied to genes from model and non-model species.

          Related collections

          Author and article information

          Journal
          Gene
          Gene
          Elsevier BV
          1879-0038
          0378-1119
          Nov 01 2013
          : 530
          : 1
          Affiliations
          [1 ] Centre of Marine Sciences, CCMAR-CIMAR Associate Laboratory, University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal. Electronic address: rsmartin@ualg.pt.
          Article
          S0378-1119(13)00960-8
          10.1016/j.gene.2013.07.052
          23954228
          5af294a8-472c-4565-9ec2-93bd4a4c9b96
          History

          18S,18S ribosomal RNA,ACTB,ACTH,ANOVA,Arβ,CAH,CAM,CILP,CYP,Ca(2+)-calmodulin,DAX1,DBD,DMSO,DNA-binding domain,Dosage-sensitive sex reversal in Adrenal Hypoplasia Congenita critical region on X chromosome, gene 1,EF1α,ERα=ESR1,Erβ=ESR2,FSH,GO,Gene Ontology,Gene networks,GnRH,HPGA,HSD,IGF1,KCN,LH,MIS,MO,MS222,Müllerian inhibiting substance,N-(6-aminohexyl)-5- chloro-1-naphtalensulfonamide,Nr0B1,ORF,Osmoregulation,PKC,PRL,Pax,Promoter architecture,SCN,SF1,SHP=Nr0B2,SLC,StAR,Steroidogenesis,Steroidogenic acute regulatory protein,TFBS,TSS,Transcription binding sites,Transcription factor binding site,Tricaine methanesulfonate,W7,adrenocorticotrophic hormone,analysis of variance,androgen receptor beta,beta actin,cAMP,cartilage intermediate layer protein,congenital adrenal hypoplasia,cyclic adenosine monosphosphate,cytochrome P-450,dimethyl sulphoxide,elongation factor 1 alpha,follicle stimulating hormone,gonadotrophin releasing hormone,hydroxysteroid dehydrogenase,hypothalamic-pituitary-gonadal-adrenal axis,insulin-like growth factor I,luteinizing hormone,morpholino,oestrogen receptor alpha or 1,oestrogen receptor beta or 2,open reading frame,orphan nuclear receptor 0 B,paired box,potassium channel,prolactin,protein kinase C,qPCR,reverse-transcription quantitative polymerase chain reaction,runt-related transcription factor 2,runx 2,small heterodimer protein,sodium channel,solute carrier,steroidogenic factor 1,transcription start site
          18S, 18S ribosomal RNA, ACTB, ACTH, ANOVA, Arβ, CAH, CAM, CILP, CYP, Ca(2+)-calmodulin, DAX1, DBD, DMSO, DNA-binding domain, Dosage-sensitive sex reversal in Adrenal Hypoplasia Congenita critical region on X chromosome, gene 1, EF1α, ERα=ESR1, Erβ=ESR2, FSH, GO, Gene Ontology, Gene networks, GnRH, HPGA, HSD, IGF1, KCN, LH, MIS, MO, MS222, Müllerian inhibiting substance, N-(6-aminohexyl)-5- chloro-1-naphtalensulfonamide, Nr0B1, ORF, Osmoregulation, PKC, PRL, Pax, Promoter architecture, SCN, SF1, SHP=Nr0B2, SLC, StAR, Steroidogenesis, Steroidogenic acute regulatory protein, TFBS, TSS, Transcription binding sites, Transcription factor binding site, Tricaine methanesulfonate, W7, adrenocorticotrophic hormone, analysis of variance, androgen receptor beta, beta actin, cAMP, cartilage intermediate layer protein, congenital adrenal hypoplasia, cyclic adenosine monosphosphate, cytochrome P-450, dimethyl sulphoxide, elongation factor 1 alpha, follicle stimulating hormone, gonadotrophin releasing hormone, hydroxysteroid dehydrogenase, hypothalamic-pituitary-gonadal-adrenal axis, insulin-like growth factor I, luteinizing hormone, morpholino, oestrogen receptor alpha or 1, oestrogen receptor beta or 2, open reading frame, orphan nuclear receptor 0 B, paired box, potassium channel, prolactin, protein kinase C, qPCR, reverse-transcription quantitative polymerase chain reaction, runt-related transcription factor 2, runx 2, small heterodimer protein, sodium channel, solute carrier, steroidogenic factor 1, transcription start site

          Comments

          Comment on this article

          scite_
          0
          0
          0
          0
          Smart Citations
          0
          0
          0
          0
          Citing PublicationsSupportingMentioningContrasting
          View Citations

          See how this article has been cited at scite.ai

          scite shows how a scientific paper has been cited by providing the context of the citation, a classification describing whether it supports, mentions, or contrasts the cited claim, and a label indicating in which section the citation was made.

          Similar content252

          Cited by4