Literature DB >> 18398334

Liddle's syndrome caused by a novel missense mutation (P617L) of the epithelial sodium channel beta subunit.

Ermanno Rossi1, Enrico Farnetti, Anne Debonneville, Davide Nicoli, Chiara Grasselli, Giuseppe Regolisti, Aurelio Negro, Franco Perazzoli, Bruno Casali, Franco Mantero, Olivier Staub.   

Abstract

OBJECTIVE: The aim of the study was to search for mutations of SCNN1B and SCNN1G in an Italian family with apparently dominant autosomal transmission of a clinical phenotype consistent with Liddle's syndrome.
METHODS: Genetic analysis was performed in the proband, his relatives, and 100 control subjects. To determine the functional role of the mutation identified in the proband, we expressed the mutant or wild-type epithelial sodium channel in Xenopus laevis oocytes.
RESULTS: A novel point mutation, causing an expected substitution of a leucine residue for the second proline residue of the conserved PY motif (PPP x Y) of the beta subunit was identified in the proband. The functional expression of the mutant epithelial sodium channel in X. laevis oocytes showed a three-fold increase in the amiloride-sensitive current as compared with that of the wild-type channel.
CONCLUSION: This newly identified mutation adds to other missense mutations of the PY motif of the beta subunit of the epithelial sodium channel, thus confirming its crucial role in the regulation of the epithelial sodium channel. To our knowledge, this is the first report of Liddle's syndrome in the Italian population, confirmed by genetic and functional analysis, with the identification of a gain-of-function mutation not previously reported.

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Year:  2008        PMID: 18398334     DOI: 10.1097/HJH.0b013e3282f85dfe

Source DB:  PubMed          Journal:  J Hypertens        ISSN: 0263-6352            Impact factor:   4.844


  12 in total

1.  Hsp70 promotes epithelial sodium channel functional expression by increasing its association with coat complex II and its exit from endoplasmic reticulum.

Authors:  Rebecca A Chanoux; Amal Robay; Calla B Shubin; Catherine Kebler; Laurence Suaud; Ronald C Rubenstein
Journal:  J Biol Chem       Date:  2012-04-10       Impact factor: 5.157

Review 2.  Liddle syndrome in a Serbian family and literature review of underlying mutations.

Authors:  Radovan Bogdanović; Vladimir Kuburović; Nataša Stajić; Sadaf S Mughal; Alina Hilger; Sanja Ninić; Sergej Prijić; Michael Ludwig
Journal:  Eur J Pediatr       Date:  2011-09-29       Impact factor: 3.183

Review 3.  ENaCs and ASICs as therapeutic targets.

Authors:  Yawar J Qadri; Arun K Rooj; Catherine M Fuller
Journal:  Am J Physiol Cell Physiol       Date:  2012-01-25       Impact factor: 4.249

4.  Hsc70 negatively regulates epithelial sodium channel trafficking at multiple sites in epithelial cells.

Authors:  Rebecca A Chanoux; Calla B Shubin; Amal Robay; Laurence Suaud; Ronald C Rubenstein
Journal:  Am J Physiol Cell Physiol       Date:  2013-07-24       Impact factor: 4.249

5.  Interactions of genetic variants with physical activity are associated with blood pressure in Chinese: the GenSalt study.

Authors:  May E Montasser; Donfeng Gu; Jing Chen; Lawrence C Shimmin; Charles Gu; Tanika N Kelly; Cashell E Jaquish; Treva Rice; Dabeeru C Rao; Jie Cao; Jichun Chen; De-Pei Liu; Paul K Whelton; Jiang He; James E Hixson
Journal:  Am J Hypertens       Date:  2011-06-09       Impact factor: 2.689

6.  Common variants in epithelial sodium channel genes contribute to salt sensitivity of blood pressure: The GenSalt study.

Authors:  Qi Zhao; Dongfeng Gu; James E Hixson; De-Pei Liu; Dabeeru C Rao; Cashell E Jaquish; Tanika N Kelly; Fanghong Lu; Jixiang Ma; Jianjun Mu; Lawrence C Shimmin; Jichun Chen; Hao Mei; L Lee Hamm; Jiang He
Journal:  Circ Cardiovasc Genet       Date:  2011-05-11

7.  Associations of epithelial sodium channel genes with blood pressure changes and hypertension incidence: the GenSalt study.

Authors:  Xueli Yang; Jiang He; Dongfeng Gu; James E Hixson; Jianfeng Huang; Dabeeru C Rao; Lawrence C Shimmin; Jichun Chen; Treva K Rice; Jianxin Li; Karen Schwander; Tanika N Kelly
Journal:  Am J Hypertens       Date:  2014-04-15       Impact factor: 2.689

8.  Three Reportedly Unrelated Families With Liddle Syndrome Inherited From a Common Ancestor.

Authors:  Luca Pagani; Yoan Diekmann; Marco Sazzini; Sara De Fanti; Maurizio Rondinelli; Enrico Farnetti; Bruno Casali; Amelia Caretto; Francesca Novara; Orsetta Zuffardi; Paolo Garagnani; Franco Mantero; Mark G Thomas; Donata Luiselli; Ermanno Rossi
Journal:  Hypertension       Date:  2017-12-11       Impact factor: 10.190

9.  Phenotype-genotype analysis in two Chinese families with Liddle syndrome.

Authors:  Ling Gong; Jinxing Chen; Liying Shao; Weihua Song; Rutai Hui; Yibo Wang
Journal:  Mol Biol Rep       Date:  2014-01-29       Impact factor: 2.316

10.  A Therapeutic Challenge: Liddle's Syndrome Managed with Amiloride during Pregnancy.

Authors:  Amelia Caretto; Liviana Primerano; Francesca Novara; Orsetta Zuffardi; Stefano Genovese; Maurizio Rondinelli
Journal:  Case Rep Obstet Gynecol       Date:  2014-08-25
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