Literature DB >> 1732736

Sequential expression of multiple POU proteins during amphibian early development.

C S Hinkley1, J F Martin, D Leibham, M Perry.   

Abstract

The octamer motif is a common cis-acting regulatory element that functions in the transcriptional control regions of diverse genes and in viral origins of replication. The ability of a consensus octamer motif to stimulate transcription of a histone H2B promoter in frog oocytes suggests that oocytes contain a transcriptionally active octamer-binding protein(s). We show here that frog oocytes and developing embryos contain multiple octamer-binding proteins that are expressed in a sequential manner during early development. Sequences encoding three novel octamer binding-proteins were isolated from Xenopus cDNA libraries by virtue of their homology with the DNA binding (POU) domain of Oct-1. The predicted POU domains of these proteins were most highly related to mammalian Oct-3 (also termed Oct-4), a germ line-specific gene required for mouse early development. Transcripts from these amphibian POU-domain genes were most abundant during early embryogenesis and absent from most adult somatic tissues. One of the genes, termed Oct-60, was primarily expressed as a maternal transcript localized in the animal hemisphere in mature oocytes. The protein encoded by this gene was present in oocytes and early embryos until the gastrula stage of development. Transcripts from a second POU-domain gene, Oct-25, were present at low levels in oocytes and early embryos and were dramatically upregulated during early gastrulation. In contrast to the Oct-60 mRNA, translation of Oct-25 mRNA appeared to be developmentally regulated, since the corresponding protein was detected in embryos during gastrulation but not in oocytes or rapidly cleaving embryos. Transcripts from the third POU protein gene, Oct-91, were induced after the midblastula transition and reached their highest levels of accumulation during late gastrulation. The expression of all three genes decreased during late gastrulation and early neurulation. By analogy with other members of the POU-domain gene family, the products of these genes may play critical roles in the determination of cell fate and the regulation of cell proliferation.

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Year:  1992        PMID: 1732736      PMCID: PMC364253          DOI: 10.1128/mcb.12.2.638-649.1992

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  40 in total

Review 1.  Regulation of transcription and cell identity by POU domain proteins.

Authors:  G Ruvkun; M Finney
Journal:  Cell       Date:  1991-02-08       Impact factor: 41.582

2.  The ubiquitous octamer-binding protein Oct-1 contains a POU domain with a homeo box subdomain.

Authors:  R A Sturm; G Das; W Herr
Journal:  Genes Dev       Date:  1988-12       Impact factor: 11.361

3.  The pituitary-specific transcription factor GHF-1 is a homeobox-containing protein.

Authors:  M Bodner; J L Castrillo; L E Theill; T Deerinck; M Ellisman; M Karin
Journal:  Cell       Date:  1988-11-04       Impact factor: 41.582

4.  MyoD is a sequence-specific DNA binding protein requiring a region of myc homology to bind to the muscle creatine kinase enhancer.

Authors:  A B Lassar; J N Buskin; D Lockshon; R L Davis; S Apone; S D Hauschka; H Weintraub
Journal:  Cell       Date:  1989-09-08       Impact factor: 41.582

5.  Repression of the IgH enhancer in teratocarcinoma cells associated with a novel octamer factor.

Authors:  M J Lenardo; L Staudt; P Robbins; A Kuang; R C Mulligan; D Baltimore
Journal:  Science       Date:  1989-01-27       Impact factor: 47.728

6.  The Oct-1 homoeodomain directs formation of a multiprotein-DNA complex with the HSV transactivator VP16.

Authors:  S Stern; M Tanaka; W Herr
Journal:  Nature       Date:  1989-10-19       Impact factor: 49.962

7.  Expression of a large family of POU-domain regulatory genes in mammalian brain development.

Authors:  X He; M N Treacy; D M Simmons; H A Ingraham; L W Swanson; M G Rosenfeld
Journal:  Nature       Date:  1989-07-06       Impact factor: 49.962

8.  A tissue-specific transcription factor containing a homeodomain specifies a pituitary phenotype.

Authors:  H A Ingraham; R P Chen; H J Mangalam; H P Elsholtz; S E Flynn; C R Lin; D M Simmons; L Swanson; M G Rosenfeld
Journal:  Cell       Date:  1988-11-04       Impact factor: 41.582

9.  The C. elegans cell lineage and differentiation gene unc-86 encodes a protein with a homeodomain and extended similarity to transcription factors.

Authors:  M Finney; G Ruvkun; H R Horvitz
Journal:  Cell       Date:  1988-12-02       Impact factor: 41.582

10.  A family of octamer-specific proteins present during mouse embryogenesis: evidence for germline-specific expression of an Oct factor.

Authors:  H R Schöler; A K Hatzopoulos; R Balling; N Suzuki; P Gruss
Journal:  EMBO J       Date:  1989-09       Impact factor: 11.598

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  34 in total

1.  Histone H2B gene transcription during Xenopus early development requires functional cooperation between proteins bound to the CCAAT and octamer motifs.

Authors:  C Hinkley; M Perry
Journal:  Mol Cell Biol       Date:  1992-10       Impact factor: 4.272

2.  Reliability of gene expression ratios for cDNA microarrays in multiconditional experiments with a reference design.

Authors:  Rainer König; Danila Baldessari; Nicolas Pollet; Christof Niehrs; Roland Eils
Journal:  Nucleic Acids Res       Date:  2004-02-13       Impact factor: 16.971

3.  Oct-3/4 regulates stem cell identity and cell fate decisions by modulating Wnt/β-catenin signalling.

Authors:  Monther Abu-Remaileh; Ariela Gerson; Marganit Farago; Gili Nathan; Irit Alkalay; Sharon Zins Rousso; Michal Gur; Abraham Fainsod; Yehudit Bergman
Journal:  EMBO J       Date:  2010-08-24       Impact factor: 11.598

4.  Repression of zygotic gene expression in the Xenopus germline.

Authors:  Thiagarajan Venkatarama; Fangfang Lai; Xueting Luo; Yi Zhou; Karen Newman; Mary Lou King
Journal:  Development       Date:  2010-02       Impact factor: 6.868

5.  Nucleotide sequence of XLPOU3 cDNA, a member of the POU domain gene family expressed in Xenopus laevis embryos.

Authors:  M Baltzinger; E Payen; P Remy
Journal:  Nucleic Acids Res       Date:  1992-04-25       Impact factor: 16.971

6.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1992-06-11       Impact factor: 16.971

7.  POU-V factors antagonize maternal VegT activity and beta-Catenin signaling in Xenopus embryos.

Authors:  Ying Cao; Doreen Siegel; Cornelia Donow; Sigrun Knöchel; Li Yuan; Walter Knöchel
Journal:  EMBO J       Date:  2007-05-31       Impact factor: 11.598

8.  Reversal of Xenopus Oct25 function by disruption of the POU domain structure.

Authors:  Ying Cao; Franz Oswald; Stephan A Wacker; Karin Bundschu; Walter Knöchel
Journal:  J Biol Chem       Date:  2010-01-11       Impact factor: 5.157

9.  Class III POU genes of zebrafish are predominantly expressed in the central nervous system.

Authors:  P Spaniol; C Bornmann; G Hauptmann; T Gerster
Journal:  Nucleic Acids Res       Date:  1996-12-15       Impact factor: 16.971

10.  A novel POU domain protein which binds to the T-cell receptor beta enhancer.

Authors:  H Messier; H Brickner; J Gaikwad; A Fotedar
Journal:  Mol Cell Biol       Date:  1993-09       Impact factor: 4.272

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