Integrative Modeling, Molecular Mechanics, and Molecular Dynamics Evaluation of Genomics Variants in KMT2C (MLL3), a Gene Involved in Kleefstra Syndrome Type 2. FASEB J 2022 May;36 Suppl 1
Date
05/14/2022Pubmed ID
35553749DOI
10.1096/fasebj.2022.36.S1.R5710Scopus ID
2-s2.0-85130006059 (requires institutional sign-in at Scopus site)Abstract
Kleefstra Syndrome (KS) is a genetic, neurodevelopmental disorder characterized by intellectual disability, infantile hypotonia, severe expressive language delay, and characteristic facial appearance, with a spectrum of other distinct clinical manifestations. Pathogenic mutations in the epigenetic modifier, type 2 lysine methyltransferase (KMT2C), are attributed to cause KS core features in individuals who are Euchromatic Histone Lysine Methyltransferase 1, EHMT1, mutation negative. These individuals are designated as having KS type 2. In this study, we made use of multidimensional approaches, including conventional genomic bioinformatics, molecular modeling, molecular mechanics, and molecular dynamics simulations, to understand and enhance the annotation and potential mechanisms by which disease-associated missense variants affect KMT2C function. In addition, we report a scoring system based on statistical integration and modeling of data derived from the structure and dynamics of KMT2C, which allows us to classify germline variants into SV (Structural Variants), DV (Dynamic Variants), SDV (Structural and Dynamic Variant), and VUS (Variant of Uncertain Significance). Moreover, these scores of disease-associated variants reflect alterations in molecular fitness when compared with tolerated, benign variants, used as controls. Thus, these studies provide data that is more refined, both structurally and functionally for each variant, compared to current annotation tools used in human genomics databases and reveal mechanisms for their dysfunction not predictable from clinical genomic methods alone. This new knowledge extends our understanding of molecular mechanisms underlying the dysfunction of KS type 2-associated genomic mutations. Lastly, by identifying KMT2C mutation-specific druggable conformations, this study builds the trajectory toward the future development of small molecules to ameliorate the symptoms of this disease.
Author List
Jorge SD, Chi YI, de Assuncao TM, Mathison AJ, Volkman B, Smith B, Lomberk G, Zimmermann MT, Urrutia RAuthors
Young-In Chi PhD Assistant Professor in the Surgery department at Medical College of WisconsinAngela Mathison PhD Assistant Professor in the Surgery department at Medical College of Wisconsin
MESH terms used to index this publication - Major topics in bold
Chromosome DeletionChromosomes, Human, Pair 9
Craniofacial Abnormalities
Genomics
Heart Defects, Congenital
Histone-Lysine N-Methyltransferase
Humans
Intellectual Disability
Molecular Dynamics Simulation
Mutation
