MCB
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
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 Chang, A. C.-M.
Right arrow Articles by Reddel, R. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chang, A. C.-M.
Right arrow Articles by Reddel, R. R.

 Previous Article  |  Next Article 

Molecular and Cellular Biology, December 2005, p. 10604-10610, Vol. 25, No. 23
0270-7306/05/$08.00+0     doi:10.1128/MCB.25.23.10604-10610.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

The Murine Stanniocalcin 1 Gene Is Not Essential for Growth and Development

Andy C.-M. Chang,1 Jeon Cha,1 Frank Koentgen,2,{dagger} and Roger R. Reddel1*

Children's Medical Research Institute, 214 Hawkesbury Road, Westmead, NSW 2145, Australia,1 Walter and Eliza Hall Institute of Medical Research, Parkville, VIC 3050, Australia2

Received 17 June 2005/ Returned for modification 11 July 2005/ Accepted 10 September 2005

The stanniocalcin 1 (STC1) gene is expressed in a wide variety of tissues, including the kidney, prostate, thyroid, bone, and ovary. STC1 protein is considered to have roles in many physiological processes, including bone development, reproduction, wound healing, angiogenesis, and modulation of inflammatory response. In fish, STC1 is a hormone that is secreted by the corpuscles of Stannius and is involved in calcium and phosphate homeostasis. To determine the role of STC1 in mammals, we generated Stc1-null mice by gene targeting. The number of Stc1/ mice obtained was in accordance with Mendelian ratios, and both males and females produced offspring normally. No anatomical or histological abnormalities were detected in any tissues. Our results demonstrated that Stc1 function is not essential for growth or reproduction in the mouse.


* Corresponding author. Mailing address: Children's Medical Research Institute, 214 Hawkesbury Road, Westmead, Sydney, NSW 2145, Australia. Phone: 61296872800. Fax: 61296872120. E-mail: rreddel{at}cmri.usyd.edu.au.

{dagger} Present address: Ozgene Pty Ltd., P.O. Box 1368, Canning Vale, WA 6970, Australia.


Molecular and Cellular Biology, December 2005, p. 10604-10610, Vol. 25, No. 23
0022-538X/05/$08.00+0     doi:10.1128/MCB.25.23.10604-10610.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. J. Virol. Eukaryot. Cell
Microbiol. Mol. Biol. Rev. Clin. Vaccine Immunol. All ASM Journals

Copyright © 2005 by the American Society for Microbiology. All rights reserved.