Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0001051
Title: Ankyrin-B syndrome: Enhanced cardiac function balance by risk of cardiac death and premature senescence
Authors: Mohler P.J.
Healy J.A.
Xue H.
Puca A.A.
Kline C.F.
Allingham R.R. 
Kranias E.G.
Rockman H.A.
Bennett V.
Keywords: ankyrin
ankyrin b
unclassified drug
ANK2 protein, human
Ank2 protein, mouse
ankyrin
Africa
animal cell
animal experiment
article
controlled study
disease association
disease severity
Europe
female
genetic variability
genotype
heart arrhythmia
heart death
heart disease
heart function
heart muscle cell
heart muscle contractility
human
human cell
in vitro study
lifespan
mouse
nonhuman
nucleotide sequence
phenotypic variation
premature aging
prevalence
risk assessment
senescence
aging
animal
C57BL mouse
cell aging
death
echocardiography
genetics
heart contraction
heart disease
methodology
pathology
phenotype
physiology
risk
syndrome
Aging
Animals
Ankyrins
Cell Aging
Death
Echocardiography
Heart Diseases
Humans
Mice
Mice, Inbred C57BL
Myocardial Contraction
Phenotype
Risk
Syndrome
Issue Date: 2007
Citation: Mohler P.J., Healy J.A., Xue H., Puca A.A., Kline C.F., Allingham R.R., Kranias E.G., Rockman H.A., Bennett V. (2007). Ankyrin-B syndrome: Enhanced cardiac function balance by risk of cardiac death and premature senescence. PLoS ONE 2 (10) : e1051. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0001051
Rights: Attribution 4.0 International
Abstract: Here we report the unexpected finding that specific human ANK2 variants represent a new example of balanced human variants. The prevalence of certain ANK2 (encodes ankyrin-B) variants range from 2 percent of European individuals to 8 percent in individuals from West Africa. Ankyrin-B variants associated with severe human arrhythmia phenotypes (eg E1425G, V1516D, R1788W) were rare in the general population. Variants associated with less severe clinical and in vitro phenotypes were unexpectedly common. Studies with the ankyrin-B+/- mouse reveal both benefits of enhanced cardiac contractility, as well as costs in earlier senescence and reduced lifespan. Together these findings suggest a constellation of traits that we term "ankyrin-B syndrome", which may contribute to both aging-related disorders and enhanced cardiac function. � 2007 Mohler et al.
Source Title: PLoS ONE
URI: https://scholarbank.nus.edu.sg/handle/10635/161863
ISSN: 19326203
DOI: 10.1371/journal.pone.0001051
Rights: Attribution 4.0 International
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