Literature DB >> 2335516

Multiple regulatory elements determine adrenocortical expression of steroid 21-hydroxylase.

D A Rice1, M S Kronenberg, A R Mouw, L D Aitken, A Franklin, B P Schimmer, K L Parker.   

Abstract

Steroid 21-hydroxylase (21-OHase) is specifically expressed at high levels in the adrenal cortex, where it is required for the synthesis of mineralocorticoids and glucocorticoids. In this study, we have investigated the regulatory elements in the 21-OHase promoter region which contribute to the expression of this gene in Y1 adrenocortical cells. Eight potential regulatory elements in the 5'-flanking region of the 21-OHase gene were identified by DNase I footprinting and gel mobility shift experiments. Some of these footprints were produced by nuclear extracts from many cell lines, whereas other interactions were seen only when using nuclear extracts from Y1 adrenocortical and MA-10 Leydig tumor cells. Mutation of most of the elements markedly decreased the expression of a 21-OHase gene transfected into Y1 cells, thus documenting their functional importance for expression. Moreover, oligonucleotides containing the sequences of two related elements at -65 and -210, which share the heptamer AGGTCAG, increased the activity of a heterologous promoter in a Y1 cell-specific manner. Collectively, these results demonstrate that expression of 21-OHase in Y1 adrenocortical cells requires interactions among multiple cis-acting elements and regulatory proteins.

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Year:  1990        PMID: 2335516

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  9 in total

1.  CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency families.

Authors:  P J Sinnott; C Livieri; M Sampietro; M Marconi; R Harris; F Severi; T Strachan
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

2.  Effects of mutating different steroidogenic factor-1 protein regions on gene regulation.

Authors:  D Lopez; A C Nackley; W Shea-Eaton; J Xue; B P Schimmer; M P McLean
Journal:  Endocrine       Date:  2001-04       Impact factor: 3.633

3.  The orphan receptors NGFI-B and steroidogenic factor 1 establish monomer binding as a third paradigm of nuclear receptor-DNA interaction.

Authors:  T E Wilson; T J Fahrner; J Milbrandt
Journal:  Mol Cell Biol       Date:  1993-09       Impact factor: 4.272

4.  Family studies of the steroid 21-hydroxylase and complement C4 genes define 11 haplotypes in classical congenital adrenal hyperplasia in The Netherlands.

Authors:  P F Koppens; T Hoogenboezem; D J Halley; C A Barendse; A J Oostenbrink; H J Degenhart
Journal:  Eur J Pediatr       Date:  1992-12       Impact factor: 3.183

5.  The orphan nuclear receptor NGFI-B regulates expression of the gene encoding steroid 21-hydroxylase.

Authors:  T E Wilson; A R Mouw; C A Weaver; J Milbrandt; K L Parker
Journal:  Mol Cell Biol       Date:  1993-02       Impact factor: 4.272

6.  Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations.

Authors:  A Wedell; E M Ritzén; B Haglund-Stengler; H Luthman
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-01       Impact factor: 11.205

7.  Adrenocortical function and regulation of the steroid 21-hydroxylase gene in NGFI-B-deficient mice.

Authors:  P A Crawford; Y Sadovsky; K Woodson; S L Lee; J Milbrandt
Journal:  Mol Cell Biol       Date:  1995-08       Impact factor: 4.272

Review 8.  Impact of ACTH Signaling on Transcriptional Regulation of Steroidogenic Genes.

Authors:  Carmen Ruggiero; Enzo Lalli
Journal:  Front Endocrinol (Lausanne)       Date:  2016-03-29       Impact factor: 5.555

Review 9.  The role of polymorphism in various potential genes on polycystic ovary syndrome susceptibility and pathogenesis.

Authors:  Hiral Chaudhary; Jalpa Patel; Nayan K Jain; Rushikesh Joshi
Journal:  J Ovarian Res       Date:  2021-09-26       Impact factor: 4.234

  9 in total

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