Journal
MOLECULAR AND CELLULAR ENDOCRINOLOGY
Volume 239, Issue 1-2, Pages 45-53Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.mce.2005.04.006
Keywords
prolactin; cyclin D1; Stat5; Oct-1
Categories
Funding
- NCI NIH HHS [R01 CA78312, R01 CA078312] Funding Source: Medline
Ask authors/readers for more resources
Prolactin (PRL) modulates proliferation in the mammary gland and other tissues, in part through inducing transcription of cyclin D 1, a key regulator of G, phase cell cycle progression. We showed previously that PRL, via Jak2, induces binding of Stat5 to a distal GAS site (GAS 1) in the cyclin D I promoter. However, full promoter activity requires additional regions, and in this paper we explored PRL-induced activity at sites other than GAS1. We defined a second PRL-responsive region spanning -254 to -180 that contains a second GAS site (GAS2) and an Oct-1 binding site. Although mutational analysis indicated independence from GAS2, proximal promoter activity remained Stat5-dependent, suggesting alternative mechanisms. EMSA showed that Oct-1 binds the -254 to -180 region and that PRL decreased Oct-1 binding, leading to increased PRL-responsiveness of the proximal cyclin D I promoter in multiple cell lines. This suggests a role for Oct-1 in PRL-dependent control of cyclin D I transcription. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available