Literature DB >> 26875730

A Pit-1 Binding Site Adjacent to E-box133 in the Rat PRL Promoter is Necessary for Pulsatile Gene Expression Activity.

Sudeep Bose1,2, Surajit Ganguly3, Sachin Kumar4, Fredric R Boockfor5.   

Abstract

Recent evidence reveals that prolactin gene expression (PRL-GE) in mammotropes occurs in pulses, but the molecular process(es) underlying this phenomenon remains unclear. Earlier, we have identified an E-box (E-box133) in the rat PRL promoter that binds several circadian elements and is critical for this dynamic process. Preliminary analysis revealed a Pit-1 binding site (P2) located immediately adjacent to this E-box133 raising the possibility that some type of functional relationship may exist between these two promoter regions. In this study, using serum shocked GH3 cell culture system to synchronize PRL-GE activity, we determined that Pit-1 gene expression occurred in pulses with time phases similar to that for PRL. Interestingly, EMSA analysis not only confirmed Pit-1 binding to the P2 site, but also revealed an interaction with factor(s) binding to the adjacent E-box133 promoter element. Additionally, down-regulation of Pit-1 by siRNA reduced PRL levels during pulse periods. Thus, using multiple evidences, our results demonstrate clearly that the Pit-1 P2 site is necessary for PRL-GE elaboration. Furthermore, the proximity of this critical Pit-1 binding site (P2) and the E-box133 element coupled with the evidences of a site-to-site protein interactions suggest that the process of PRL-GE pulse activity might involve more dynamic and intricate cross-talks between promoter elements that may span some, or all, of the proximal region of the PRL promoter in driving its pulsatile expression.

Entities:  

Keywords:  E-box; Pit-1; Pituitary; Prolactin; Pulses; Transcription

Mesh:

Substances:

Year:  2016        PMID: 26875730     DOI: 10.1007/s11064-016-1843-y

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  34 in total

1.  PRL gene expression in individual living mammotropes displays distinct functional pulses that oscillate in a noncircadian temporal pattern.

Authors:  Spencer L Shorte; Gilles M Leclerc; Rafael Vazquez-Martinez; David C Leaumont; William J Faught; L Stephen Frawley; Fredric R Boockfor
Journal:  Endocrinology       Date:  2002-03       Impact factor: 4.736

2.  Interaction of basal positive and negative transcription elements controls repression of the proximal rat prolactin promoter in nonpituitary cells.

Authors:  S M Jackson; C A Keech; D J Williamson; A Gutierrez-Hartmann
Journal:  Mol Cell Biol       Date:  1992-06       Impact factor: 4.272

3.  Structure-function analysis of the rat prolactin promoter: phasing requirements of proximal cell-specific elements.

Authors:  C Harvey; S M Jackson; S K Siddiqui; A Gutierrez-Hartmann
Journal:  Mol Endocrinol       Date:  1991-06

4.  Structure of Pit-1 POU domain bound to DNA as a dimer: unexpected arrangement and flexibility.

Authors:  E M Jacobson; P Li; A Leon-del-Rio; M G Rosenfeld; A K Aggarwal
Journal:  Genes Dev       Date:  1997-01-15       Impact factor: 11.361

5.  A pituitary POU domain protein, Pit-1, activates both growth hormone and prolactin promoters transcriptionally.

Authors:  H J Mangalam; V R Albert; H A Ingraham; M Kapiloff; L Wilson; C Nelson; H Elsholtz; M G Rosenfeld
Journal:  Genes Dev       Date:  1989-07       Impact factor: 11.361

6.  Discrete cis-active genomic sequences dictate the pituitary cell type-specific expression of rat prolactin and growth hormone genes.

Authors:  C Nelson; E B Crenshaw; R Franco; S A Lira; V R Albert; R M Evans; M G Rosenfeld
Journal:  Nature       Date:  1986 Aug 7-13       Impact factor: 49.962

7.  CLOCK is involved in the circadian transactivation of peroxisome-proliferator-activated receptor alpha (PPARalpha) in mice.

Authors:  Katsutaka Oishi; Hidenori Shirai; Norio Ishida
Journal:  Biochem J       Date:  2005-03-15       Impact factor: 3.857

Review 8.  A family of POU-domain and Pit-1 tissue-specific transcription factors in pituitary and neuroendocrine development.

Authors:  H A Ingraham; V R Albert; R P Chen; E B Crenshaw 3d; H P Elsholtz; X He; M S Kapiloff; H J Mangalam; L W Swanson; M N Treacy
Journal:  Annu Rev Physiol       Date:  1990       Impact factor: 19.318

9.  MicroRNAs regulate pituitary development, and microRNA 26b specifically targets lymphoid enhancer factor 1 (Lef-1), which modulates pituitary transcription factor 1 (Pit-1) expression.

Authors:  Zichao Zhang; Sergio Florez; Arthur Gutierrez-Hartmann; James F Martin; Brad A Amendt
Journal:  J Biol Chem       Date:  2010-08-31       Impact factor: 5.157

10.  The circadian clock component BMAL1 is a critical regulator of p21WAF1/CIP1 expression and hepatocyte proliferation.

Authors:  Aline Gréchez-Cassiau; Béatrice Rayet; Fabienne Guillaumond; Michèle Teboul; Franck Delaunay
Journal:  J Biol Chem       Date:  2007-12-17       Impact factor: 5.157

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