|
|
||||||||
Regular Article |
a Department of Biotechnology, Institute for Animal Science and Animal Behaviour (FAL), Mariensee, Neustadt, Germany
b Gene Expression Programme, European Molecular Biology Laboratory, Heidelberg, Germany
ABSTRACT
POU transcription factors are involved in transcriptional regulation during early embryonic development and cell differentiation. Oct-4, a member of this family, has been shown to be under strict regulation during murine development. The expression of Oct-4 correlates with the undifferentiated cell phenotype of the mouse preimplantation embryo. In this study, expression of a gene construct consisting of selected parts of the region upstream from the murine Oct-4 gene as promoter/enhancer, enhanced green fluorescent protein (EGFP) as reporter and the five exons of the murine Oct-4 gene (GOF18-
PE EGFP) was evaluated in murine, porcine, and bovine preimplantation embryos. For comparison, expression of the endogenous Oct-4 gene was also analyzed in all three species by immunocytochemistry. The transgene construct was microinjected into zygotes cultured in vitro to various developmental stages. The EGFP fluorescence was visualized in developing embryos by excitation with blue light at different days following microinjection and showed similar expression patterns in all three species. Most embryos displayed a mosaic pattern of transgene expression. The EGFP fluorescence was not restricted to the inner cell mass (ICM) but was also seen in trophoblastic cells. An affinity-purified polyclonal antibody specific to Oct-4 was used for immunocytochemical analysis of in vivo- and in vitro-derived bovine and porcine blastocysts and also of in vivo-derived murine blastocysts. In the in vivo-derived murine embryos, Oct-4 protein was detectable in the ICM but not the trophectoderm, whereas in porcine and bovine blastocysts, derived in vivo or in vitro, Oct-4 protein was detected in both the ICM and the trophectoderm. Thus, in the two large animal species, Oct-4 expression from the endogenous gene was clearly not restricted to the pluripotent cells of the early embryo. These results show that Oct-4 regulation differs between these species and that the presence of Oct-4 protein may not be sufficient for selection of undifferentiated cell lines in domestic animals.
First decision: 26 April 2000.
1 Correspondence: Heiner Niemann, Department of Biotechnology, Institut für Tierzucht und Tierverhalten, (FAL) Mariensee, 31535 Neustadt, Germany. FAX: 49 5034 871 101; niemann{at}tzv.fal.de
2 Current address: University of Pennsylvania, New Bolton Center, Center for Animal Transgenesis and Germ Cell Research, Philadelphia, PA 19348.
This article has been cited by other articles:
![]() |
S. Goel, M. Fujihara, N. Minami, M. Yamada, and H. Imai Expression of NANOG, but not POU5F1, points to the stem cell potential of primitive germ cells in neonatal pig testis Reproduction, June 1, 2008; 135(6): 785 - 795. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Lavial, H. Acloque, F. Bertocchini, D. J. MacLeod, S. Boast, E. Bachelard, G. Montillet, S. Thenot, H. M. Sang, C. D. Stern, et al. The Oct4 homologue PouV and Nanog regulate pluripotency in chicken embryonic stem cells Development, October 1, 2007; 134(19): 3549 - 3563. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Wuensch, F. A. Habermann, S. Kurosaka, R. Klose, V. Zakhartchenko, H.-D. Reichenbach, F. Sinowatz, K. J. McLaughlin, and E. Wolf Quantitative Monitoring of Pluripotency Gene Activation after Somatic Cloning in Cattle Biol Reprod, June 1, 2007; 76(6): 983 - 991. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Nganvongpanit, H. Muller, F. Rings, M. Hoelker, D. Jennen, E. Tholen, V. Havlicek, U. Besenfelder, K. Schellander, and D. Tesfaye Selective degradation of maternal and embryonic transcripts in in vitro produced bovine oocytes and embryos using sequence specific double-stranded RNA. Reproduction, May 1, 2006; 131(5): 861 - 874. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Cauffman, H. Van de Velde, I. Liebaers, and A. Van Steirteghem Oct-4 mRNA and protein expression during human preimplantation development Mol. Hum. Reprod., March 1, 2005; 11(3): 173 - 181. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Vejlsted, B. Avery, M. Schmidt, T. Greve, N. Alexopoulos, and P. Maddox-Hyttel Ultrastructural and Immunohistochemical Characterization of the Bovine Epiblast Biol Reprod, March 1, 2005; 72(3): 678 - 686. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Kurosaka, S. Eckardt, and K. J. McLaughlin Pluripotent Lineage Definition in Bovine Embryos by Oct4 Transcript Localization Biol Reprod, November 1, 2004; 71(5): 1578 - 1582. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. M. Mitalipov, H.-C. Kuo, J. D. Hennebold, and D. P. Wolf Oct-4 Expression in Pluripotent Cells of the Rhesus Monkey Biol Reprod, December 1, 2003; 69(6): 1785 - 1792. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Lazzari, C. Wrenzycki, D. Herrmann, R. Duchi, T. Kruip, H. Niemann, and C. Galli Cellular and Molecular Deviations in Bovine In Vitro-Produced Embryos Are Related to the Large Offspring Syndrome Biol Reprod, September 1, 2002; 67(3): 767 - 775. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Ezashi, D. Ghosh, and R. M. Roberts Repression of Ets-2-Induced Transactivation of the Tau Interferon Promoter by Oct-4 Mol. Cell. Biol., December 1, 2001; 21(23): 7883 - 7891. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Pesce and H. R. Scholer Oct-4: Gatekeeper in the Beginnings of Mammalian Development Stem Cells, July 1, 2001; 19(4): 271 - 278. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |