This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Thiel, C.
Right arrow Articles by Körner, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Thiel, C.
Right arrow Articles by Körner, C.

 Previous Article  |  Next Article 

Molecular and Cellular Biology, August 2006, p. 5615-5620, Vol. 26, No. 15
0270-7306/06/$08.00+0     doi:10.1128/MCB.02391-05
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Targeted Disruption of the Mouse Phosphomannomutase 2 Gene Causes Early Embryonic Lethality

Christian Thiel,1* Torben Lübke,2 Gert Matthijs,3 Kurt von Figura,2 and Christian Körner1

Universitaetskinderklinik Heidelberg, Abteilung I, Friedrich Karls Universitaet Heidelberg, Im Neuenheimer Feld 153, 69120 Heidelberg, Germany,1 Institut fuer Biochemie II, Georg-August-Universitaet Goettingen, Heinrich-Dueker-Weg 12, D-37073 Gottingen, Germany,2 University of Leuven, Center for Human Genetics, Herestraat 49, B-3000 Leuven, Belgium3

Received 15 December 2005/ Returned for modification 13 February 2006/ Accepted 2 March 2006

Mutations in the cytosolic enzyme phosphomannomutase 2 (PMM2), which catalyzes the conversion of mannose-6-phosphate to mannose-1-phosphate, cause the most common form of congenital disorders of glycosylation, termed CDG-Ia. It is an inherited multisystemic disease with severe neurological impairment. To study the pathophysiology of CDG-Ia and to investigate possible therapeutic approaches, we generated a mouse model for CDG-Ia by targeted disruption of the Pmm2 gene. Heterozygous mutant mice appeared normal in development, gross anatomy, and fertility. In contrast, embryos homozygous for the Pmm2-null allele were recovered in embryonic development at days 2.5 to 3.5. These results indicate that Pmm2 is essential for early development of mice. Mating experiments of heterozygous mice with wild-type mice could further show that transmission of the female Pmm2-null allele is impaired.


* Corresponding author. Mailing address: Universitaetskinderklinik und Poliklinik, Abteilung Kinderheilkunde I, Im Neuenheimer Feld 153, D-69120 Heidelberg, Germany. Phone: 49(0)6221-564817. Fax: 49(0)6221-565565. E-mail: Christian.Thiel{at}med.uni-heidelberg.de.


Molecular and Cellular Biology, August 2006, p. 5615-5620, Vol. 26, No. 15
0270-7306/06/$08.00+0     doi:10.1128/MCB.02391-05
Copyright © 2006, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Badejo, A. A., Eltelib, H. A., Fukunaga, K., Fujikawa, Y., Esaka, M. (2009). Increase in Ascorbate Content of Transgenic Tobacco Plants Overexpressing the Acerola (Malpighia glabra) Phosphomannomutase Gene. Plant Cell Physiol 50: 423-428 [Abstract] [Full Text]  
  • Veiga-da-Cunha, M., Vleugels, W., Maliekal, P., Matthijs, G., Van Schaftingen, E. (2008). Mammalian Phosphomannomutase PMM1 Is the Brain IMP-sensitive Glucose-1,6-bisphosphatase. J. Biol. Chem. 283: 33988-33993 [Abstract] [Full Text]  
  • Hoeberichts, F. A., Vaeck, E., Kiddle, G., Coppens, E., van de Cotte, B., Adamantidis, A., Ormenese, S., Foyer, C. H., Zabeau, M., Inze, D., Perilleux, C., Van Breusegem, F., Vuylsteke, M. (2008). A Temperature-sensitive Mutation in the Arabidopsis thaliana Phosphomannomutase Gene Disrupts Protein Glycosylation and Triggers Cell Death. J. Biol. Chem. 283: 5708-5718 [Abstract] [Full Text]  
  • Cromphout, K., Vleugels, W., Heykants, L., Schollen, E., Keldermans, L., Sciot, R., D'Hooge, R., De Deyn, P. P., von Figura, K., Hartmann, D., Korner, C., Matthijs, G. (2006). The Normal Phenotype of Pmm1-Deficient Mice Suggests that Pmm1 Is Not Essential for Normal Mouse Development. Mol. Cell. Biol. 26: 5621-5635 [Abstract] [Full Text]