Literature DB >> 32857907

Comprehensive Behavioral Phenotyping of a 16p11.2 Del Mouse Model for Neurodevelopmental Disorders.

Joseph F Lynch1, Sarah L Ferri2, Christopher Angelakos3, Hannah Schoch4, Thomas Nickl-Jockschat5, Arnold Gonzalez6, William Timothy O'Brien6, Ted Abel2.   

Abstract

The microdeletion of copy number variant 16p11.2 is one of the most common genetic mutations associated with neurodevelopmental disorders, such as Autism Spectrum Disorders (ASDs). Here, we describe our comprehensive behavioral phenotyping of the 16p11.2 deletion line developed by Alea Mills on a C57BL/6J and 129S1/SvImJ F1 background (Delm ). Male and female Delm mice were tested in developmental milestones as preweanlings (PND2-PND12), and were tested in open field activity, elevated zero maze, rotarod, novel object recognition, fear conditioning, social approach, and other measures during post-weaning (PND21), adolescence (PND42), and adulthood (>PND70). Developmentally, Delm mice show distinct weight reduction that persists into adulthood. Delm males also have reduced grasp reflexes and limb strength during development, but no other reflexive deficits whereas Delm females show limb strength deficits and decreased sensitivity to heat. In a modified version of a rotarod task that measures balance and coordinated motor activity, Delm males, but not females, show improved performance at high speeds. Delm males and females also show age-specific reductions in anxiety-like behavior compared with WTs, but neither sex show deficits in a social preference task. When assessing learning and memory, Delm males and females show age-specific impairments in a novel object or spatial object recognition, but no deficits in contextual fear memory. This work extends the understanding of the behavioral phenotypes seen with 16p11.2 deletion by emphasizing age and sex-specific deficits; important variables to consider when studying mouse models for neurodevelopmental disorders. LAY
SUMMARY: Autism spectrum disorder is a common neurodevelopmental disorder that causes repetitive behavior and impairments in social interaction and communication. Here, we assess the effects of one of the most common genetic alterations in ASDs, a deletion of one copy of 29 genes, using a mouse model. These animals show differences in behavior between males and females and across ages compared with control animals, including changes in development, cognition, and motor coordination. Autism Res 2020, 13: 1670-1684.
© 2020 International Society for Autism Research and Wiley Periodicals LLC. © 2020 International Society for Autism Research and Wiley Periodicals LLC.

Entities:  

Keywords:  16p11.2; autism spectrum disorders; behavior; copy number variant; mouse model; neurodevelopmental disorders; phenotype

Mesh:

Year:  2020        PMID: 32857907      PMCID: PMC7990053          DOI: 10.1002/aur.2357

Source DB:  PubMed          Journal:  Autism Res        ISSN: 1939-3806            Impact factor:   5.216


  53 in total

1.  16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions.

Authors:  Mu Yang; Elena J Mahrt; Freeman Lewis; Gillian Foley; Thomas Portmann; Ricardo E Dolmetsch; Christine V Portfors; Jacqueline N Crawley
Journal:  Autism Res       Date:  2015-02-07       Impact factor: 5.216

2.  A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology.

Authors:  Eugenia Migliavacca; Christelle Golzio; Katrin Männik; Ian Blumenthal; Edwin C Oh; Louise Harewood; Jack A Kosmicki; Maria Nicla Loviglio; Giuliana Giannuzzi; Loyse Hippolyte; Anne M Maillard; Ali Abdullah Alfaiz; Mieke M van Haelst; Joris Andrieux; James F Gusella; Mark J Daly; Jacques S Beckmann; Sébastien Jacquemont; Michael E Talkowski; Nicholas Katsanis; Alexandre Reymond
Journal:  Am J Hum Genet       Date:  2015-04-30       Impact factor: 11.025

3.  Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome.

Authors:  Mu Yang; Rong Mao; Georgia Panagiotakos; Thomas Portmann; Jacob Ellegood; Gul Dolen; Patrick L Bader; Brad A Grueter; Carleton Goold; Elaine Fisher; Katherine Clifford; Pavitra Rengarajan; David Kalikhman; Darren Loureiro; Nay L Saw; Zhou Zhengqui; Michael A Miller; Jason P Lerch; Mark Henkelman; Mehrdad Shamloo; Robert C Malenka; Jacqueline N Crawley; Ricardo E Dolmetsch
Journal:  Cell Rep       Date:  2014-05-01       Impact factor: 9.423

Review 4.  What Is the Male-to-Female Ratio in Autism Spectrum Disorder? A Systematic Review and Meta-Analysis.

Authors:  Rachel Loomes; Laura Hull; William Polmear Locke Mandy
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2017-04-05       Impact factor: 8.829

5.  Limited effects of ozone exposure during pregnancy on physical and neurobehavioral development of CD-1 mice.

Authors:  G Bignami; B Musi; G Dell'Omo; G Laviola; E Alleva
Journal:  Toxicol Appl Pharmacol       Date:  1994-12       Impact factor: 4.219

6.  Pharmacological Inhibition of ERK Signaling Rescues Pathophysiology and Behavioral Phenotype Associated with 16p11.2 Chromosomal Deletion in Mice.

Authors:  Joanna Pucilowska; Joseph Vithayathil; Marco Pagani; Caitlin Kelly; J Colleen Karlo; Camilla Robol; Ilaria Morella; Alessandro Gozzi; Riccardo Brambilla; Gary E Landreth
Journal:  J Neurosci       Date:  2018-06-22       Impact factor: 6.167

7.  Ultrasonic songs of male mice.

Authors:  Timothy E Holy; Zhongsheng Guo
Journal:  PLoS Biol       Date:  2005-11-01       Impact factor: 8.029

8.  Comprehensive Analysis of the 16p11.2 Deletion and Null Cntnap2 Mouse Models of Autism Spectrum Disorder.

Authors:  Daniela Brunner; Patricia Kabitzke; Dansha He; Kimberly Cox; Lucinda Thiede; Taleen Hanania; Emily Sabath; Vadim Alexandrov; Michael Saxe; Elior Peles; Alea Mills; Will Spooren; Anirvan Ghosh; Pamela Feliciano; Marta Benedetti; Alice Luo Clayton; Barbara Biemans
Journal:  PLoS One       Date:  2015-08-14       Impact factor: 3.240

9.  Linking spatial gene expression patterns to sex-specific brain structural changes on a mouse model of 16p11.2 hemideletion.

Authors:  Vinod Jangir Kumar; Nicola M Grissom; Sarah E McKee; Hannah Schoch; Nicole Bowman; Robbert Havekes; Manoj Kumar; Stephen Pickup; Harish Poptani; Teresa M Reyes; Mike Hawrylycz; Ted Abel; Thomas Nickl-Jockschat
Journal:  Transl Psychiatry       Date:  2018-05-29       Impact factor: 6.222

10.  Association and mutation analyses of 16p11.2 autism candidate genes.

Authors:  Ravinesh A Kumar; Christian R Marshall; Judith A Badner; Timothy D Babatz; Zohar Mukamel; Kimberly A Aldinger; Jyotsna Sudi; Camille W Brune; Gerald Goh; Samer Karamohamed; James S Sutcliffe; Edwin H Cook; Daniel H Geschwind; William B Dobyns; Stephen W Scherer; Susan L Christian
Journal:  PLoS One       Date:  2009-02-26       Impact factor: 3.240

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  1 in total

Review 1.  Emerging behavioral and neuroimaging biomarkers for early and accurate characterization of autism spectrum disorders: a systematic review.

Authors:  Chandrakanta S Hiremath; Kommu John Vijay Sagar; B K Yamini; Akhila S Girimaji; Raghavendra Kumar; Sanivarapu Lakshmi Sravanti; Hansashree Padmanabha; K N Vykunta Raju; M Thomas Kishore; Preeti Jacob; Jitender Saini; Rose D Bharath; Shekhar P Seshadri; Manoj Kumar
Journal:  Transl Psychiatry       Date:  2021-01-13       Impact factor: 6.222

  1 in total

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