Evidence map›Paper›PMID 1732736›Full record

ArticleMolecular and cellular biology1992

Sequential expression of multiple POU proteins during amphibian early development.

C S Hinkley, J F Martin, D Leibham, M Perry

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 102 citations in OpenAlex.

  1. Zygotic genome activation in the chicken: a comparative review.Cellular and molecular life sciences : CMLS · 2020
    Review
  2. Review
  3. Article
  4. A novel role forDevelopment (Cambridge, England) · 2018
    Article
  5. Article
  6. Review
  7. Establishing pluripotency in early development.Biochimica et biophysica acta · 2015
    Review
  8. Review
  9. Article
  10. Article
  11. On the origin of POU5F1.BMC biology · 2013
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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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

4 authors.

C S HinkleyDepartment of Biochemistry and Molecular Biology, University of Texas M. D. Anderson Cancer Center, Houston 77030.
J F Martin
D Leibham
M Perry

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Kathrin Milbury · 1985 to 2026
$290.8M
REGULATION OF XENOPUS HISTONE GENE TRANSCRIPTIONR01HD022025 · NICHD · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI PERRY, W M · 1986 to 1994
–
NCI NIH HHS CA-16672NICHD NIH HHS HD22025
6 · The paper itself

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.

Indexed as

Amino Acid SequenceAnimalsBase SequenceBinding SitesBlotting, NorthernCloning, MolecularDNA-Binding ProteinsEmbryo, NonmammalianGene ExpressionHost Cell Factor C1Molecular Sequence DataOctamer Transcription Factor-1Octamer Transcription Factor-3OocytesRecombinant Fusion ProteinsTranscription FactorsDNA-Binding ProteinsHost Cell Factor C1Octamer Transcription Factor-1Octamer Transcription Factor-3POU2F1 protein, XenopusRecombinant Fusion ProteinsTranscription FactorsXenopus Proteins

Identifiers

PMID1732736
PMCPMC364253
OpenAlexW2234712136

What OpenQuestion holds

Textmetadata
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.