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Molecular and Cellular Biology, July 2007, p. 5120-5127, Vol. 27, No. 14
0270-7306/07/$08.00+0 doi:10.1128/MCB.00215-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Center of Molecular and Human Genetics, Children's Research Institute, Columbus, Ohio 43205
Received 5 February 2007/ Returned for modification 28 March 2007/ Accepted 27 April 2007
To investigate in vivo roles of a murine hypothalamic homeobox gene, Bsx, we generated and analyzed two mutant alleles, Bsx
HD and BsxlacZ. Bsx
HD lacks the homeodomain, and BsxlacZ is an insertion of a lacZ reporter gene. Bsx-lacZ expression was detected in the hypothalamus and pineal gland and reiterates Bsx expression. Bsx homozygous mutant mice were born at the expected Mendelian ratio, but their growth was impaired. Offspring from Bsx homozygous mutant females exhibited a low survival rate due to a nursing defect. Mammary glands of the mutant females developed normally during pregnancy; however, they involuted quickly after parturition. These results demonstrate that Bsx is required for postnatal growth and maintenance of lactating mammary glands. Thus, mouse Bsx is likely involved in systemic control of suppression of apoptosis of postpartum mammary epithelial cells.
Published ahead of print on 7 May 2007.
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