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Impulsivity is a heritable trait in rodents and associated with a novel quantitative trait locus on chromosome 1.

Authors
  • Jupp, Bianca
  • Pitzoi, Silvia
  • Petretto, Enrico
  • Mar, Adam C
  • Oliver, Yolanda Pena
  • Jordan, Emily R
  • Taylor, Stephanie
  • Atanur, Santosh S
  • Srivastava, Prashant K
  • Saar, Kathrin
  • Hubner, Norbert
  • Sommer, Wolfgang H
  • Staehlin, Oliver
  • Spanagel, Rainer
  • Robinson, Emma S
  • Schumann, Gunter
  • Moreno, Margarita
  • Everitt, Barry J
  • Robbins, Trevor W
  • Aitman, Timothy J
  • And 1 more
Publication Date
Apr 02, 2020
Source
Apollo - University of Cambridge Repository
Keywords
Language
English
License
Unknown
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Abstract

Impulsivity describes the tendency to act prematurely without appropriate foresight and is symptomatic of a number of neuropsychiatric disorders. Although a number of genes for impulsivity have been identified, no study to date has carried out an unbiased, genome-wide approach to identify genetic markers associated with impulsivity in experimental animals. Herein we report a linkage study of a six-generational pedigree of adult rats phenotyped for one dimension of impulsivity, namely premature responding on the five-choice serial reaction time task, combined with genome wide sequencing and transcriptome analysis to identify candidate genes associated with the expression of the impulsivity trait. Premature responding was found to be heritable (h2 = 13-16%), with significant linkage (LOD 5.2) identified on chromosome 1. Fine mapping of this locus identified a number of polymorphic candidate genes, however only one, beta haemoglobin, was differentially expressed in both the founder strain and F6 generation. These findings provide novel insights into the genetic substrates and putative neurobiological mechanisms of impulsivity with broader translational relevance for impulsivity-related disorders in humans. / This research was funded by the Medical Research Council (G0802729) and a grant from the European Community’s Sixth Framework Programme (‘IMAGEN’ LSHM-CT-2007-037286). This paper reflects only the author’s views, and the Community is not liable for any use that may be made of the information contained therein. The Behavioural and Clinical Neuroscience Institute (BCNI) at Cambridge University is supported by a core award from the Medical Research Council (G1000183) and the Wellcome Trust (093875/Z/10/Z). BJ was supported by an AXA Trust Research Fellowship. MM was supported by a grant from the Ministerio Economía y Competitividad, Spanish Government (PSI2015-70037-R MINECO-FEDER).

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