Hormone-dependent recruitment of NF-Y to the uteroglobin gene enhancer associated with chromatin remodeling in rabbit endometrial epithelium

Citation
A. Scholz et al., Hormone-dependent recruitment of NF-Y to the uteroglobin gene enhancer associated with chromatin remodeling in rabbit endometrial epithelium, J BIOL CHEM, 274(7), 1999, pp. 4017-4026
Citations number
86
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF BIOLOGICAL CHEMISTRY
ISSN journal
00219258 → ACNP
Volume
274
Issue
7
Year of publication
1999
Pages
4017 - 4026
Database
ISI
SICI code
0021-9258(19990212)274:7<4017:HRONTT>2.0.ZU;2-X
Abstract
Expression of the rabbit uteroglobin gene is hormonally induced in cells of the endometrial epithelium during the preimplantation phase of pregnancy. Here we show that progesterone activation of the gene is mediated by two cl usters of hormone responsive elements located between 2.4 and 2.7 kilobase pairs upstream of the transcriptional start site. Between these two cluster s, genomic footprinting studies in the intact endometrial epithelium reveal the hormone-inducible occupancy of several cis-acting elements. One of the protected elements shows sequence homology to the consensus binding site o f the transcription factor NF-Y, which binds to the element in gel shift ex periments. This uteroglobin Y box is essential for enhancer activity in tra nsient transfection experiments with endometrial and non-endometrial cell l ines, in accordance with the ubiquitous expression of NF-Y. To understand w hy binding of this ubiquitous factor to the uteroglobin Y box in endometriu m depends on hormone induction, we examined the chromatin structure of the relevant gene region. In the uninduced state, the enhancer region appears t o be organized into positioned nucleosomes. Upon hormone induction, this nu cleosomal pattern is lost and the enhancer region becomes hypersensitive to nucleases, suggesting that a hormone-induced change in the local chromatin structure unmasks previously unaccessible binding sites for transcription factors. Our results emphasize the limitations of using transient transfect ion assays for the functional analysis of cis-acting elements and underline the need for including the native chromatin organization in this kind of s tudies.