De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features

被引:3
|
作者
Andrews, Jonathan C. [1 ,2 ]
Mok, Jung-Wan [1 ,2 ]
Kanca, Oguz [1 ,2 ]
Jangam, Sharayu [1 ,2 ]
Tifft, Cynthia [3 ]
Macnamara, Ellen F. [3 ]
Russell, Bianca E. [4 ,5 ]
Wang, Lee-kai [5 ]
Nelson, Stanley F. [5 ]
Bellen, Hugo J. [1 ,2 ,6 ]
Yamamoto, Shinya [1 ,2 ,6 ]
Malicdan, May Christine V. [3 ,7 ]
Wangler, Michael F. [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX USA
[2] Jan & Dan Duncan Neurol Res Inst, 1250 Moursund St,Suite NRI1050, Houston, TX 77030 USA
[3] Natl Human Genome Res Inst, Undiagnosed Dis Program, NIH, Bethesda, MD USA
[4] Univ Calif Los Angeles, Dept Pediat, Div Genet, Los Angeles, CA USA
[5] Univ Calif Los Angeles, Inst Precis Hlth, David Geffen Sch Med, Los Angeles, CA USA
[6] Baylor Coll Med, Dept Neurosci, Houston, TX USA
[7] NIH, Med Genet Branch, Rm 10C-103,10 Ctr Dr, Bethesda, MD 20892 USA
关键词
Actin; Drosophila; Dysmorphic features; Intellectual disability; MRTFB; SERUM RESPONSE FACTOR; TRANSCRIPTION-FACTOR-B; CARDIAC GENE-EXPRESSION; MYOCARDIN; SRF; FUSION; COFACTOR; DIFFERENTIATION; LOCALIZATION; REQUIREMENT;
D O I
10.1016/j.gim.2023.100833
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose: Myocardin-related transcription factor B (MRTFB) is an important transcriptional regulator, which promotes the activity of an estimated 300 genes but is not known to underlie a Mendelian disorder.Methods: Probands were identified through the efforts of the Undiagnosed Disease Network. Because the MRTFB protein is highly conserved between vertebrate and invertebrate model organisms, we generated a humanized Drosophila model expressing the human MRTFB protein in the same spatial and temporal pattern as the fly gene. Actin binding assays were used to validate the effect of the variants on MRTFB.Results: Here, we report 2 pediatric probands with de novo variants in MRTFB (p.R104G and p.A91P) and mild dysmorphic features, intellectual disability, global developmental delays, speech apraxia, and impulse control issues. Expression of the variants within wing tissues of a fruit fly model resulted in changes in wing morphology. The MRTFBR104G and MRTFBA91P variants also display a decreased level of actin binding within critical RPEL domains, resulting in increased transcriptional activity and changes in the organization of the actin cytoskeleton.Conclusion: The MRTFBR104G and MRTFBA91P variants affect the regulation of the protein and underlie a novel neurodevelopmental disorder. Overall, our data suggest that these variants act as a gain of function.(c) 2023 by American College of Medical Genetics and Genomics. Published by Elsevier Inc.
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页数:17
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