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Multiple promoters in the WNK1 gene: one controls expression of a kidney-specific kinase-defective isoform.


ABSTRACT: WNK1 is a serine-threonine kinase, the expression of which is affected in pseudohypoaldosteronism type II, a Mendelian form of arterial hypertension. We characterized human WNK1 transcripts to determine the molecular mechanisms governing WNK1 expression. We report the presence of two promoters generating two WNK1 isoforms with a complete kinase domain. Further variations are achieved by the use of two polyadenylation sites and tissue-specific splicing. We also determined the structure of a kidney-specific isoform regulated by a third promoter and starting at a novel exon. This transcript is kinase defective and has a predominant expression in the kidney compared to the other WNK1 isoforms, with, furthermore, a highly restricted expression profile in the distal convoluted tubule. We confirmed that the ubiquitous and kidney-specific promoters are functional in several cells lines and identified core promoters and regulatory elements. In particular, a strong enhancer element upstream from the kidney-specific exon seems specific to renal epithelial cells. Thus, control of human WNK1 gene expression of kinase-active or -deficient isoforms is mediated predominantly through the use of multiple transcription initiation sites and tissue-specific regulatory elements.

SUBMITTER: Delaloy C 

PROVIDER: S-EPMC309643 | biostudies-literature | 2003 Dec

REPOSITORIES: biostudies-literature

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Multiple promoters in the WNK1 gene: one controls expression of a kidney-specific kinase-defective isoform.

Delaloy Celine C   Lu Jingyu J   Houot Anne-Marie AM   Disse-Nicodeme Sandra S   Gasc Jean-Marie JM   Corvol Pierre P   Jeunemaitre Xavier X  

Molecular and cellular biology 20031201 24


WNK1 is a serine-threonine kinase, the expression of which is affected in pseudohypoaldosteronism type II, a Mendelian form of arterial hypertension. We characterized human WNK1 transcripts to determine the molecular mechanisms governing WNK1 expression. We report the presence of two promoters generating two WNK1 isoforms with a complete kinase domain. Further variations are achieved by the use of two polyadenylation sites and tissue-specific splicing. We also determined the structure of a kidne  ...[more]

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