Medical Journals

Stem Cell Regulatory Function Mediated by Expression of a Novel Mouse Oct4 Pseudogene.

Authors:
  • Lin Huey
  • Shabbir Arsalan
  • Molnar Merced
  • Lee Techung

From: Department of Biochemistry, SUNY at Buffalo, 3435 Main Street, Buffalo, NY 14214, USA.

Biochemical and biophysical research communications

  • Publish Date: Mar 2007
  • ISSN: 0006-291X
  • Volume: 355
  • Issue: 1
  • Pages: 111-6
  • Medium: Print
  • Language: English
  • Citation (JAMA): Lin Huey, Shabbir Arsalan, Molnar Merced, et al. Stem Cell Regulatory Function Mediated by Expression of a Novel Mouse Oct4 Pseudogene.. Biochem. Biophys. Res. Commun. Mar 2007;355:111-6

Abstract

Multiple pseudogenes have been proposed for embryonic stem (ES) cell-specific genes, and their abundance suggests that some of these potential pseudogenes may be functional. ES cell-specific expression of Oct4 regulates stem cell pluripotency and self-renewing state. Although Oct4 expression has been reported in adult tissues during gene reprogramming, the detected Oct4 signal might be contributed by Oct4 pseudogenes. Among the multiple Oct4 transcripts characterized here is a approximately 1 kb clone derived from P19 embryonal carcinoma stem cells, which shares a approximately 87% sequence homology with the parent Oct4 gene, and has the potential of encoding an 80-amino acid product (designated as Oct4P1). Adenoviral expression of Oct4P1 in mesenchymal stem cells promotes their proliferation and inhibits their osteochondral differentiation. These dual effects of Oct4P1 are reminiscent of the stem cell regulatory function of the parent Oct4, and suggest that Oct4P1 may be a functional pseudogene or a novel Oct4-related gene with a unique function in stem cells.

Mesh Headings (Keywords): Animals, Cell Differentiation, DNA Primers, Embryonic Stem Cells, Gene Expression Regulation, Mesenchymal Stem Cells, Mice, Octamer Transcription Factor-3, Peptide Fragments, Pseudogenes, Recombinant Proteins, Reverse Transcriptase Polymerase Chain Reaction, Swine


Check for Full Text / PubMed Unique Identifier (PMID): 17280643


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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