Literature DB >> 16103266

Association of NEDD4L ubiquitin ligase with essential hypertension.

Christopher J Russo1, Efthymia Melista, Jing Cui, Anita L DeStefano, George L Bakris, Athanasios J Manolis, Haralambos Gavras, Clinton T Baldwin.   

Abstract

NEDD4L is a ubiquitin ligase that controls cell surface expression of kidney epithelial Na+ channels by ubiquitin-mediated endocytosis and lysosome targeting. Thus, it is a significant determinant of Na+ reabsorption in the distal nephron. The NEDD4L gene is located on human chromosome 18q21 within several blood pressure quantitative trait loci, including those for familial orthostatic hypotension, essential hypertension, pulse pressure, and systolic blood pressure response to postural challenge. Because of the importance of NEDD4L to Na+ balance, many of these studies have proposed that mutations in NEDD4L may be responsible for these blood pressure phenotypes. To test this hypothesis, we fine-mapped the NEDD4L region in 2 families with orthostatic hypotension, which we previously reported to be linked to human chromosome 18q21 but failed to implicate NEDD4L in these families. We also typed multiple NEDD4L single-nucleotide polymorphisms (SNPs) in a collection of US whites, Greek whites, and African-Americans individuals with essential hypertension. A significant association between several SNPs and hypertension was observed in all 3 populations. One of the SNPs associated in African Americans is known to result in premature truncation of the NEDD4L protein. Thus, genetic variation in NEDD4L may play a role in the development or progression of some forms of abnormal blood pressure.

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Year:  2005        PMID: 16103266     DOI: 10.1161/01.HYP.0000178594.63193.c0

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  31 in total

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Journal:  J Biol Chem       Date:  2010-02-19       Impact factor: 5.157

2.  Haplotype diversity in four genes (CLCNKA, CLCNKB, BSND, NEDD4L) involved in renal salt reabsorption.

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Review 3.  Physiologic regulation of the epithelial sodium channel by phosphatidylinositides.

Authors:  Oleh Pochynyuk; Vladislav Bugaj; James D Stockand
Journal:  Curr Opin Nephrol Hypertens       Date:  2008-09       Impact factor: 2.894

Review 4.  Hereditary determinants of human hypertension: strategies in the setting of genetic complexity.

Authors:  Pei-an Betty Shih; Daniel T O'Connor
Journal:  Hypertension       Date:  2008-04-14       Impact factor: 10.190

Review 5.  Genetic architecture of complex traits predisposing to nephropathy: hypertension.

Authors:  Steven C Hunt
Journal:  Semin Nephrol       Date:  2010-03       Impact factor: 5.299

Review 6.  NEDD4-2 (NEDD4L): the ubiquitin ligase for multiple membrane proteins.

Authors:  Pranay Goel; Jantina A Manning; Sharad Kumar
Journal:  Gene       Date:  2014-11-26       Impact factor: 3.688

7.  Identification of candidate genes for dyslexia susceptibility on chromosome 18.

Authors:  Thomas S Scerri; Silvia Paracchini; Andrew Morris; I Laurence MacPhie; Joel Talcott; John Stein; Shelley D Smith; Bruce F Pennington; Richard K Olson; John C DeFries; Anthony P Monaco; Alex J Richardson
Journal:  PLoS One       Date:  2010-10-28       Impact factor: 3.240

8.  Prostasin: a possible candidate gene for human hypertension.

Authors:  Haidong Zhu; Dehuang Guo; Ke Li; Weili Yan; Yuande Tan; Xiaoling Wang; Frank A Treiber; Julie Chao; Harold Snieder; Yanbin Dong
Journal:  Am J Hypertens       Date:  2008-06-26       Impact factor: 2.689

9.  Genetic analysis of diabetic nephropathy on chromosome 18 in African Americans: linkage analysis and dense SNP mapping.

Authors:  Caitrin W McDonough; Meredith A Bostrom; Lingyi Lu; Pamela J Hicks; Carl D Langefeld; Jasmin Divers; Josyf C Mychaleckyj; Barry I Freedman; Donald W Bowden
Journal:  Hum Genet       Date:  2009-12       Impact factor: 4.132

10.  Genetic variation of NEDD4L is associated with essential hypertension in female Kazakh general population: a case-control study.

Authors:  Nanfang Li; Hongmei Wang; Jin Yang; Ling Zhou; Jing Hong; Yanying Guo; Wenli Luo; Jianhang Chang
Journal:  BMC Med Genet       Date:  2009-12-09       Impact factor: 2.103

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