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De Novo Mutation in an Enhancer of EBF3 in simplex autism

  • Author(s): Padhi, Evin;
  • Hayeck, Tristan;
  • Mannion, Brandon;
  • Chatterjee, Sumantra;
  • Byrska-Bishop, Marta;
  • Musunuri, Rajeeva;
  • Narzisi, Giuseppe;
  • Abhyankar, Avinash;
  • Cheng, Zhang;
  • Hunter, Riana;
  • Akiyama, Jennifer;
  • Fries, Lauren;
  • Ng, Jeffrey;
  • Stong, Nick;
  • Allen, Andrew;
  • Dickel, Diane;
  • Bernier, Raphael;
  • Gorkin, David;
  • Pennacchio, Len;
  • Zody, Michael;
  • Turner, Tychele
  • et al.

Published Web Location

https://www.biorxiv.org/content/10.1101/2020.08.28.270751v1
No data is associated with this publication.
Abstract

Previous research in autism and other neurodevelopmental disorders (NDDs) has indicated an important contribution of de novo protein-coding variants within specific genes. The role of de novo noncoding variation has been observable as a general increase in genetic burden but has yet to be resolved to individual functional elements. In this study, we assessed whole-genome sequencing data in 2,671 families with autism, with a specific focus on de novo variation in enhancers with previously characterized in vivo activity. We identified three independent de novo mutations limited to individuals with autism in the enhancer hs737. These mutations result in similar phenotypic characteristics, affect enhancer activity in vitro , and preferentially occur in AAT motifs in the enhancer with predicted disruptions of transcription factor binding. We also find that hs737 is enriched for copy number variation in individuals with NDDs, is dosage sensitive in the human population, is brain-specific, and targets the NDD gene EBF3 that is genome-wide significant for protein coding de novo variants, demonstrating the importance of understanding all forms of variation in the genome.

One Sentence Summary

Whole-genome sequencing in thousands of families reveals variants relevant to simplex autism in a brain enhancer of the well-established neurodevelopmental disorder gene EBF3 .

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