3 years ago

Heterozygous variants in ACTL6A, encoding a component of the BAF complex, are associated with intellectual disability

Heterozygous variants in ACTL6A, encoding a component of the BAF complex, are associated with intellectual disability
Yangjin Bae, Christine Eng, Yaping Yang, Andrew T. Gunter, Philippe M. Campeau, Brett H. Graham, Jill A. Rosenfeld, Chester W. Brown, Bert B.A. Vries, Alyssa A. Tran, Justine Rousseau, Lindsay C. Burrage, Yuqing Chen, Servi J.C. Stevens, Alexander P.A. Stegmann, Marwan Shinawi, Ralitza H. Gavrilova, I-Wen Song, Ronit Marom, Julie D. Kaplan, James T. Lu, Richard A. Gibbs, Mahim Jain, Brendan Lee
Pathogenic variants in genes encoding components of the BRG1-associated factor (BAF) chromatin remodeling complex have been associated with intellectual disability syndromes. We identified heterozygous, novel variants in ACTL6A, a gene encoding a component of the BAF complex, in three subjects with varying degrees of intellectual disability. Two subjects have missense variants affecting highly conserved amino acid residues within the actin-like domain. Missense mutations in the homologous region in yeast actin were previously reported to be dominant lethal and were associated with impaired binding of the human ACTL6A to β-actin and BRG1. A third subject has a splicing variant that creates an in-frame deletion. Our findings suggest that the variants identified in our subjects may have a deleterious effect on the function of the protein by disturbing the integrity of the BAF complex. Thus, ACTL6A gene mutation analysis should be considered in patients with intellectual disability, learning disabilities, or developmental language disorder. Pathogenic variants in genes that closely interact with the BRG1-associated factor (BAF) complex have been associated with intellectual disability. We identified heterozygous variants ACTL6A, a scaffold component of the BAF complex, in three subjects with developmental delay and varying degree of learning disabilities. All variants are predicted to result in loss-of-function. We suggest that sequencing of ACTL6A should be considered in the diagnostic work-up of developmental delay and learning disabilities.

Publisher URL: http://onlinelibrary.wiley.com/resolve/doi

DOI: 10.1002/humu.23282

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.