Functional phenotype variations of two novel KV7.1 mutations identified in patients with Long QT syndrome

Background The slow delayed rectifier potassium current IKs is crucial for the repolarization of the cardiac action potential. It is conducted by the voltage‐gated channel KV7.1 encoded by KCNQ1, together with its β‐subunit KCNE1. Loss‐of‐function (LOF) mutations in KCNQ1 have been associated with h...

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Veröffentlicht in:Pacing and clinical electrophysiology 2020-02, Vol.43 (2), p.210-216
Hauptverfasser: Hammami Bomholtz, Sofia, Refaat, Marwan, Buur Steffensen, Annette, David, Jens‐Peter, Espinosa, Karin, Nussbaum, Robert, Wojciak, Julianne, Hjorth Bentzen, Bo, Scheinman, Melvin, Schmitt, Nicole
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container_end_page 216
container_issue 2
container_start_page 210
container_title Pacing and clinical electrophysiology
container_volume 43
creator Hammami Bomholtz, Sofia
Refaat, Marwan
Buur Steffensen, Annette
David, Jens‐Peter
Espinosa, Karin
Nussbaum, Robert
Wojciak, Julianne
Hjorth Bentzen, Bo
Scheinman, Melvin
Schmitt, Nicole
description Background The slow delayed rectifier potassium current IKs is crucial for the repolarization of the cardiac action potential. It is conducted by the voltage‐gated channel KV7.1 encoded by KCNQ1, together with its β‐subunit KCNE1. Loss‐of‐function (LOF) mutations in KCNQ1 have been associated with heritable cardiac arrhythmias such as Long QT syndrome (LQTS). This disease is characterized by prolonged ventricular repolarization and propensity to ventricular tachyarrhythmia that may lead to syncope, cardiac arrest, and sudden death. We aimed to functionally characterize two KV7.1 mutations (p.A150T and p.L374H) identified in two independent LQTS patients with different severity of disease phenotype, family history, and co‐segregation of LQTS. Methods We performed whole‐cell patch clamp recordings in CHO‐K1 cells, and confocal imaging in Madin‐Darby Canine Kidney (MDCK) cells. Results IKs‐A150T showed significantly decreased current amplitudes from above +20 mV (approximately 52% decrease at +40 mV), but demonstrated cell membrane localization similar to wild‐type (WT). IKs‐L374H, however, exhibited a complete LOF compared to WT channels. Confocal imaging showed endoplasmic reticulum retention of the channel in MDCK cells. Mimicking the heterozygous state of the patients by co‐expressing WT and mutant subunits resulted in an approximately 22% decrease in current at +40 mV for A150T. The L374H mutation showed a more pronounced effect (62% reduction at +40 mV compared to WT channel). Conclusion Both mutations, KV7.1 A150T and L374H, led to loss of channel function. The degree of LOF may mirror the disease phenotype observed in the patients.
doi_str_mv 10.1111/pace.13870
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It is conducted by the voltage‐gated channel KV7.1 encoded by KCNQ1, together with its β‐subunit KCNE1. Loss‐of‐function (LOF) mutations in KCNQ1 have been associated with heritable cardiac arrhythmias such as Long QT syndrome (LQTS). This disease is characterized by prolonged ventricular repolarization and propensity to ventricular tachyarrhythmia that may lead to syncope, cardiac arrest, and sudden death. We aimed to functionally characterize two KV7.1 mutations (p.A150T and p.L374H) identified in two independent LQTS patients with different severity of disease phenotype, family history, and co‐segregation of LQTS. Methods We performed whole‐cell patch clamp recordings in CHO‐K1 cells, and confocal imaging in Madin‐Darby Canine Kidney (MDCK) cells. Results IKs‐A150T showed significantly decreased current amplitudes from above +20 mV (approximately 52% decrease at +40 mV), but demonstrated cell membrane localization similar to wild‐type (WT). IKs‐L374H, however, exhibited a complete LOF compared to WT channels. Confocal imaging showed endoplasmic reticulum retention of the channel in MDCK cells. Mimicking the heterozygous state of the patients by co‐expressing WT and mutant subunits resulted in an approximately 22% decrease in current at +40 mV for A150T. The L374H mutation showed a more pronounced effect (62% reduction at +40 mV compared to WT channel). Conclusion Both mutations, KV7.1 A150T and L374H, led to loss of channel function. The degree of LOF may mirror the disease phenotype observed in the patients.</description><identifier>ISSN: 0147-8389</identifier><identifier>EISSN: 1540-8159</identifier><identifier>DOI: 10.1111/pace.13870</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Action potential ; cardiac electrophysiology ; Cell membranes ; Electrocardiography ; Endoplasmic reticulum ; Genotype &amp; phenotype ; IKs current ; KCNQ1 protein ; Localization ; Long QT syndrome ; Mimicry ; Mutants ; Mutation ; Phenotypes ; Phenotypic variations ; Potassium channels (voltage-gated) ; risk stratification ; Syncope ; Tachyarrhythmia ; Ventricle</subject><ispartof>Pacing and clinical electrophysiology, 2020-02, Vol.43 (2), p.210-216</ispartof><rights>2020 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0001-9482-9749 ; 0000-0002-3210-1987</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fpace.13870$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fpace.13870$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27911,27912,45561,45562</link.rule.ids></links><search><creatorcontrib>Hammami Bomholtz, Sofia</creatorcontrib><creatorcontrib>Refaat, Marwan</creatorcontrib><creatorcontrib>Buur Steffensen, Annette</creatorcontrib><creatorcontrib>David, Jens‐Peter</creatorcontrib><creatorcontrib>Espinosa, Karin</creatorcontrib><creatorcontrib>Nussbaum, Robert</creatorcontrib><creatorcontrib>Wojciak, Julianne</creatorcontrib><creatorcontrib>Hjorth Bentzen, Bo</creatorcontrib><creatorcontrib>Scheinman, Melvin</creatorcontrib><creatorcontrib>Schmitt, Nicole</creatorcontrib><title>Functional phenotype variations of two novel KV7.1 mutations identified in patients with Long QT syndrome</title><title>Pacing and clinical electrophysiology</title><description>Background The slow delayed rectifier potassium current IKs is crucial for the repolarization of the cardiac action potential. It is conducted by the voltage‐gated channel KV7.1 encoded by KCNQ1, together with its β‐subunit KCNE1. Loss‐of‐function (LOF) mutations in KCNQ1 have been associated with heritable cardiac arrhythmias such as Long QT syndrome (LQTS). This disease is characterized by prolonged ventricular repolarization and propensity to ventricular tachyarrhythmia that may lead to syncope, cardiac arrest, and sudden death. We aimed to functionally characterize two KV7.1 mutations (p.A150T and p.L374H) identified in two independent LQTS patients with different severity of disease phenotype, family history, and co‐segregation of LQTS. Methods We performed whole‐cell patch clamp recordings in CHO‐K1 cells, and confocal imaging in Madin‐Darby Canine Kidney (MDCK) cells. Results IKs‐A150T showed significantly decreased current amplitudes from above +20 mV (approximately 52% decrease at +40 mV), but demonstrated cell membrane localization similar to wild‐type (WT). IKs‐L374H, however, exhibited a complete LOF compared to WT channels. Confocal imaging showed endoplasmic reticulum retention of the channel in MDCK cells. Mimicking the heterozygous state of the patients by co‐expressing WT and mutant subunits resulted in an approximately 22% decrease in current at +40 mV for A150T. The L374H mutation showed a more pronounced effect (62% reduction at +40 mV compared to WT channel). Conclusion Both mutations, KV7.1 A150T and L374H, led to loss of channel function. The degree of LOF may mirror the disease phenotype observed in the patients.</description><subject>Action potential</subject><subject>cardiac electrophysiology</subject><subject>Cell membranes</subject><subject>Electrocardiography</subject><subject>Endoplasmic reticulum</subject><subject>Genotype &amp; phenotype</subject><subject>IKs current</subject><subject>KCNQ1 protein</subject><subject>Localization</subject><subject>Long QT syndrome</subject><subject>Mimicry</subject><subject>Mutants</subject><subject>Mutation</subject><subject>Phenotypes</subject><subject>Phenotypic variations</subject><subject>Potassium channels (voltage-gated)</subject><subject>risk stratification</subject><subject>Syncope</subject><subject>Tachyarrhythmia</subject><subject>Ventricle</subject><issn>0147-8389</issn><issn>1540-8159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNotkE9PwzAMxSMEEmNw4RNE4txhN8mWHqdpA8QkQBpco7RNWKYtKU27qd-e7o8vfn5-suQfIY8II-zrudKFGSGTE7giAxQcEokiuyYDQD5JJJPZLbmLcQMAY-BiQNyi9UXjgtdbWq2ND01XGbrXtdNHN9JgaXMI1Ie92dL3n8kI6a5tLktXGt8460xJnadV7_ZzpAfXrOky-F_6taKx82Udduae3Fi9jebh0ofkezFfzV6T5cfL22y6TCrkAImQFpkuxplOZS7AMs05l5LZXmlWsiy3UspUWCmYznUBJRZplglAtJgbZEPydL5b1eGvNbFRm9DW_X9RpUxwMRbAsz6F59TBbU2nqtrtdN0pBHXkqI4c1Ymj-pzO5ifF_gFml2jJ</recordid><startdate>202002</startdate><enddate>202002</enddate><creator>Hammami Bomholtz, Sofia</creator><creator>Refaat, Marwan</creator><creator>Buur Steffensen, Annette</creator><creator>David, Jens‐Peter</creator><creator>Espinosa, Karin</creator><creator>Nussbaum, Robert</creator><creator>Wojciak, Julianne</creator><creator>Hjorth Bentzen, Bo</creator><creator>Scheinman, Melvin</creator><creator>Schmitt, Nicole</creator><general>Wiley Subscription Services, Inc</general><scope>7TK</scope><scope>NAPCQ</scope><orcidid>https://orcid.org/0000-0001-9482-9749</orcidid><orcidid>https://orcid.org/0000-0002-3210-1987</orcidid></search><sort><creationdate>202002</creationdate><title>Functional phenotype variations of two novel KV7.1 mutations identified in patients with Long QT syndrome</title><author>Hammami Bomholtz, Sofia ; Refaat, Marwan ; Buur Steffensen, Annette ; David, Jens‐Peter ; Espinosa, Karin ; Nussbaum, Robert ; Wojciak, Julianne ; Hjorth Bentzen, Bo ; Scheinman, Melvin ; Schmitt, Nicole</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p1400-58f13ac69a28b50f3a444883ff3aa3d39bf88825f853abac0d1c2995011f1be13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Action potential</topic><topic>cardiac electrophysiology</topic><topic>Cell membranes</topic><topic>Electrocardiography</topic><topic>Endoplasmic reticulum</topic><topic>Genotype &amp; phenotype</topic><topic>IKs current</topic><topic>KCNQ1 protein</topic><topic>Localization</topic><topic>Long QT syndrome</topic><topic>Mimicry</topic><topic>Mutants</topic><topic>Mutation</topic><topic>Phenotypes</topic><topic>Phenotypic variations</topic><topic>Potassium channels (voltage-gated)</topic><topic>risk stratification</topic><topic>Syncope</topic><topic>Tachyarrhythmia</topic><topic>Ventricle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hammami Bomholtz, Sofia</creatorcontrib><creatorcontrib>Refaat, Marwan</creatorcontrib><creatorcontrib>Buur Steffensen, Annette</creatorcontrib><creatorcontrib>David, Jens‐Peter</creatorcontrib><creatorcontrib>Espinosa, Karin</creatorcontrib><creatorcontrib>Nussbaum, Robert</creatorcontrib><creatorcontrib>Wojciak, Julianne</creatorcontrib><creatorcontrib>Hjorth Bentzen, Bo</creatorcontrib><creatorcontrib>Scheinman, Melvin</creatorcontrib><creatorcontrib>Schmitt, Nicole</creatorcontrib><collection>Neurosciences Abstracts</collection><collection>Nursing &amp; Allied Health Premium</collection><jtitle>Pacing and clinical electrophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hammami Bomholtz, Sofia</au><au>Refaat, Marwan</au><au>Buur Steffensen, Annette</au><au>David, Jens‐Peter</au><au>Espinosa, Karin</au><au>Nussbaum, Robert</au><au>Wojciak, Julianne</au><au>Hjorth Bentzen, Bo</au><au>Scheinman, Melvin</au><au>Schmitt, Nicole</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional phenotype variations of two novel KV7.1 mutations identified in patients with Long QT syndrome</atitle><jtitle>Pacing and clinical electrophysiology</jtitle><date>2020-02</date><risdate>2020</risdate><volume>43</volume><issue>2</issue><spage>210</spage><epage>216</epage><pages>210-216</pages><issn>0147-8389</issn><eissn>1540-8159</eissn><abstract>Background The slow delayed rectifier potassium current IKs is crucial for the repolarization of the cardiac action potential. 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IKs‐L374H, however, exhibited a complete LOF compared to WT channels. Confocal imaging showed endoplasmic reticulum retention of the channel in MDCK cells. Mimicking the heterozygous state of the patients by co‐expressing WT and mutant subunits resulted in an approximately 22% decrease in current at +40 mV for A150T. The L374H mutation showed a more pronounced effect (62% reduction at +40 mV compared to WT channel). Conclusion Both mutations, KV7.1 A150T and L374H, led to loss of channel function. The degree of LOF may mirror the disease phenotype observed in the patients.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1111/pace.13870</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-9482-9749</orcidid><orcidid>https://orcid.org/0000-0002-3210-1987</orcidid></addata></record>
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subjects Action potential
cardiac electrophysiology
Cell membranes
Electrocardiography
Endoplasmic reticulum
Genotype & phenotype
IKs current
KCNQ1 protein
Localization
Long QT syndrome
Mimicry
Mutants
Mutation
Phenotypes
Phenotypic variations
Potassium channels (voltage-gated)
risk stratification
Syncope
Tachyarrhythmia
Ventricle
title Functional phenotype variations of two novel KV7.1 mutations identified in patients with Long QT syndrome
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