Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome.

Abstract

Mutations in components of the major spliceosome have been described in disorders with craniofacial anomalies, e.g., Nager syndrome and mandibulofacial dysostosis type Guion-Almeida. The U5 spliceosomal complex of eight highly conserved proteins is critical for pre-mRNA splicing. We identified biallelic mutations in TXNL4A, a member of this complex, in individuals with Burn-McKeown syndrome (BMKS). This rare condition is characterized by bilateral choanal atresia, hearing loss, cleft lip and/or palate, and other craniofacial dysmorphisms. Mutations were found in 9 of 11 affected families. In 8 families, affected individuals carried a rare loss-of-function mutation (nonsense, frameshift, or microdeletion) on one allele and a low-frequency 34 bp deletion (allele frequency 0.76%) in the core promoter region on the other allele. In a single highly consanguineous family, formerly diagnosed as oculo-oto-facial dysplasia, the four affected individuals were homozygous for a 34 bp promoter deletion, which differed from the promoter deletion in the other families. Reporter gene and in vivo assays showed that the promoter deletions led to reduced expression of TXNL4A. Depletion of TXNL4A (Dib1) in yeast demonstrated reduced assembly of the tri-snRNP complex. Our results indicate that BMKS is an autosomal-recessive condition, which is frequently caused by compound heterozygosity of low-frequency promoter deletions in combination with very rare loss-of-function mutations.

• Authors: Dagmar Wieczorek, William G Newman, Thomas Wieland, Tea Berulava, Maria Kaffe, Daniela Falkenstein, Christian Beetz, Elisabeth Graf, Thomas Schwarzmayr, Sofia Douzgou, Jill Clayton-Smith, Sarah B Daly, Simon G Williams, Sanjeev S Bhaskar, Jill E Urquhart, Beverley Anderson, James O'Sullivan, Odile Boute, Jasmin Gundlach, Johanna Christina Czeschik, Anthonie J van Essen, Filiz Hazan, Sarah Park, Anne Hing, Alma Kuechler, Dietmar R Lohmann, Kerstin U Ludwig, Elisabeth Mangold, Laura Steenpaß, Michael Zeschnigk, Johannes R Lemke, Charles Marques Lourenco, Ute Hehr, Eva-Christina Prott, Melanie Waldenberger, Anne C Böhmer, Bernhard Horsthemke, Raymond T O'Keefe, Thomas Meitinger, John Burn, Hermann-Josef Lüdecke, Tim M Strom
• Journal: American journal of human genetics (Am J Hum Genet) Vol. 95 Issue 6 Pg. 698-707 (Dec 04 2014) ISSN: 1537-6605 [Electronic] United States
• PMID: 25434003 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2014 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

Chemical References

• Ribonucleoprotein, U5 Small Nuclear
• TXNL4A protein, human

Topics

• Alleles
• Child, Preschool
• Choanal Atresia (diagnosis, genetics)
• Deafness (congenital, diagnosis, genetics)
• Exosomes (genetics)
• Facies
• Female
• Gene Deletion
• Gene Expression Profiling
• Gene Frequency
• Genes, Reporter
• Heart Defects, Congenital (diagnosis, genetics)
• Heterozygote
• Homozygote
• Humans
• Male
• Mutation
• Oligonucleotide Array Sequence Analysis
• Pedigree
• Phenotype
• Promoter Regions, Genetic (genetics)
• Ribonucleoprotein, U5 Small Nuclear (genetics, metabolism)
• Sequence Analysis, DNA
• Spliceosomes (genetics, metabolism)