Molecular Approaches to Drug Abuse Research Volume I: Receptor Cloning, Neurotransmitter Expression, and Molecular Genetics: Research Monograph 111

1991 ◽  
Author(s):  
Theresa N. H. Lee ◽  
Author(s):  
Amber M. Jarnecke ◽  
Susan C. South

Behavior and molecular genetics informs knowledge of the etiology, structure, and development of the Five Factor Model (FFM) of personality. Behavior genetics uses quantitative modeling to parse the relative influence of nature and nurture on phenotypes that vary within the population. Behavior genetics research on the FFM has demonstrated that each domain has a heritability (proportion of variation due to genetic influences) of 40–50%. Molecular genetic methods attempt to identify specific genetic mechanisms associated with personality variation. To date, findings from molecular genetics are tentative, with significant results failing to replicate and accounting for only a small percentage of the variance. However, newer techniques hold promise for finding the “missing heritability” of FFM and related personality domains. This chapter presents an overview of commonly used behavior and molecular genetic techniques, reviews the work that has been done on the FFM domains and facets, and offers a perspective for future directions.


2001 ◽  
Vol 179 (2) ◽  
pp. 122-128 ◽  
Author(s):  
Philip J. Asherson ◽  
Sarah Curran

BackgroundTwin studies demonstrate the importance of genes and environment in the aetiology of childhood psychiatric and neurodevelopmental disorders. Advances in molecular genetics enable the identification of genes involved in complex disorders and enable the study of molecular mechanisms and gene–environment interactions.AimsTo review the role of molecular genetics studies in childhood behavioural and developmental traits.MethodMolecular approaches to complex disorders are reviewed, with examples from autism, reading disability and attention-deficit hyperactivity disorder (ADHD).ResultsThe most robust finding in ADHD is the association of a variable number tandem repeat polymorphism in exon 3 of the DRD4 gene. Other replicated associations with ADHD are outlined in the text. In autism, there is a replicated linkage finding on chromosome 7. Linkage studies in reading disability have confirmed a locus on chromosome 6 and strongly suggest one on chromosome 15.ConclusionsIn the next 5–10 years susceptibility genes for these disorders will be established. Describing their relationship to biological and behavioural function will be a far greater challenge.


2015 ◽  
Vol 125 ◽  
pp. 34-42 ◽  
Author(s):  
Sonika Ahlawat ◽  
Rekha Sharma ◽  
A. Maitra ◽  
M.S. Tantia

2017 ◽  
Vol 4 (7) ◽  
pp. 161061 ◽  
Author(s):  
Jane Melville ◽  
Margaret L. Haines ◽  
Katja Boysen ◽  
Luke Hodkinson ◽  
Andrzej Kilian ◽  
...  

Next-generation sequencing (NGS) approaches are increasingly being used to generate multi-locus data for phylogeographic and evolutionary genetics research. We detail the applicability of a restriction enzyme-mediated genome complexity reduction approach with subsequent NGS (DArTseq) in vertebrate study systems at different evolutionary and geographical scales. We present two case studies using SNP data from the DArTseq molecular marker platform. First, we used DArTseq in a large phylogeographic study of the agamid lizard Ctenophorus caudicinctus , including 91 individuals and spanning the geographical range of this species across arid Australia. A low-density DArTseq assay resulted in 28 960 SNPs, with low density referring to a comparably reduced set of identified and sequenced markers as a cost-effective approach. Second, we applied this approach to an evolutionary genetics study of a classic frog hybrid zone ( Litoria ewingii–Litoria paraewingi ) across 93 individuals, which resulted in 48 117 and 67 060 SNPs for a low- and high-density assay, respectively. We provide a docker-based workflow to facilitate data preparation and analysis, then analyse SNP data using multiple methods including Bayesian model-based clustering and conditional likelihood approaches. Based on comparison of results from the DArTseq platform and traditional molecular approaches, we conclude that DArTseq can be used successfully in vertebrates and will be of particular interest to researchers working at the interface between population genetics and phylogenetics, exploring species boundaries, gene exchange and hybridization.


2014 ◽  
Vol 8 (1) ◽  
Author(s):  
Endashaw Bekele ◽  
Walter F Bodmer ◽  
Neil Bradman ◽  
Ian W Craig ◽  
Julie Makani ◽  
...  

2014 ◽  
Vol 8 (1) ◽  
pp. 2
Author(s):  
Endashaw Bekele ◽  
Walter F Bodmer ◽  
Neil Bradman ◽  
Ian W Craig ◽  
Julie Makani ◽  
...  

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