|  Help  |  About  |  Contact Us

Publication : Lactation status influences expression of CCAAT/enhancer binding protein isoform mRNA in the mouse mammary gland.

First Author  Gigliotti AP Year  1998
Journal  J Cell Physiol Volume  174
Issue  2 Pages  232-9
PubMed ID  9428809 Mgi Jnum  J:45112
Mgi Id  MGI:1101748 Doi  10.1002/(SICI)1097-4652(199802)174:2<232::AID-JCP10>3.0.CO;2-E
Citation  Gigliotti AP, et al. (1998) Lactation status influences expression of CCAAT/enhancer bindingprotein isoform mRNA in the mouse mammary gland. J Cell Physiol 174(2):232-9
abstractText  The CCAAT/enhancer binding proteins (C/EBPs) are a highly conserved family of DNA binding proteins implicated in the transcriptional control of genes involved in cell growth and differentiation in a variety of tissues. The expression of C/EBP-alpha, beta, and delta mRNA in the normal mouse mammary gland was investigated during pregnancy, lactation, and involution via Northern blotting and in situ hybridization. Mammary gland C/EBP-alpha mRNA is detectable at low levels during pregnancy and postlactational involution. C/EBP-beta mRNA levels are elevated during pregnancy, decline slightly in midlactation, and are induced within 48 hours of the onset of involution. C/EBP-delta mRNA content is low throughout pregnancy and lactation, but increases dramatically (>100-fold) within 12 hours after the onset of postlactational involution. In situ hybridization demonstrates that mammary epithelial cells are responsible for the expression of C/EBP-delta mRNA during involution. In contrast to mammary gland, C/EBP-alpha is the predominate isoform expressed in liver with relatively low expression of C/EBP-beta and C/EBP-delta mRNA. Liver C/EBP isoform mRNA levels are unaffected by lactation status. These results demonstrate the tissue-specific regulation of C/EBPs. The pronounced sequential induction of C/EBP-delta and C/EBP-beta during postlactational involution is consistent with a role for C/EBPs in the regulation of mammary epithelial cell apoptosis.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

2 Authors

3 Bio Entities

Trail: Publication

0 Expression