Article

Elements of 'missing heritability'.

Center for Cardiovascular Genetics, Brown Foundation Institute of Molecular Medicine, The University of Texas Health Science Center and Texas Heart Institute, Houston, Texas 77030, USA.
Current opinion in cardiology (impact factor: 2.66). 03/2012; 27(3):197-201. DOI:10.1097/HCO.0b013e328352707d pp.197-201
Source: PubMed

ABSTRACT To discuss the basis of 'missing heritability', which has emerged as an enigma in the post-genome-wide association studies (GWAS) era.
Alleles identified through GWAS account for a relatively small fraction of heritability of the complex phenotypes. Accordingly, a significant part of heritability of the complex traits remains unaccounted for ('missing heritability'). Recent findings offer several explanations, including overestimation of heritability of the complex traits and underestimation of the effects of alleles identified through GWAS. In addition, yet-to-be identified common as well as rare alleles might in part explain the 'missing heritability'. Moreover, gene-gene (epistasis) and gene-environmental interactions might explain another fraction of heritability of complex traits. Moreover, transgenerational epigenetic changes, regulated in part by microRNAs, might also contribute to the 'missing heritability'.
The new findings suggest a multifarious nature of the 'missing heritability'. The findings de-emphasize the focus on delineating the basis of 'missing heritability' and shift the focus to elucidation of the molecular mechanisms by which genomic and genetic factors govern the pathogenesis of the complex phenotypes.

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Keywords

'missing heritability'
 
Alleles
 
complex phenotypes
 
complex traits
 
delineating
 
findings de-emphasize
 
gene-environmental interactions
 
gene-gene
 
genetic factors
 
GWAS
 
GWAS account
 
molecular mechanisms
 
multifarious nature
 
new findings
 
pathogenesis
 
post-genome-wide association studies
 
rare alleles
 
small fraction
 
transgenerational epigenetic changes
 
unaccounted
 

Ali J Marian