Complex translocation disrupting TCF4 and altering TCF4 isoform expression segregates as mild autosomal dominant intellectual disability. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Maduro, Valerie; Pusey, Barbara; Cherukuri, Praveen; Atkins, Paul; du Souich, Christèle; Rupps, Rosemarie; Limbos, Marjolaine; Adams, David; Bhatt, Samarth; Eydoux, Patrice; Links, Amanda; Lehman, Anna; Malicdan, May; Mason, Christopher; Morimoto, Marie; Mullikin, James; Sear, Andrew; Van Karnebeek, Clara; Stankiewicz, Pawel; Gahl, William; Toro, Camilo; Boerkoel, Cornelius
• Is Part Of: Orphanet journal of rare diseases. Volume 11:Issue 1(2016)
• Page Start: 1
• Page End: 15
• Publication Date: 2016-12
• Subjects: Intellectual disability -- Promoter utilization -- Pitt-Hopkins syndrome -- TCF4 -- Gene expression -- Translocation -- Transcriptome -- RNAseq; Rare diseases -- Periodicals; Genetic disorders -- Periodicals; Orphan drugs -- Periodicals; 616
• DOI: 10.1186/s13023-016-0439-6
• Languages: English
• ISSNs: 1750-1172

Abstract

Abstract Background Mutations ofTCF4, which encodes a basic helix-loop-helix transcription factor, cause Pitt-Hopkins syndrome (PTHS) via multiple genetic mechanisms.TCF4 is a complex locus expressing multiple transcripts by alternative splicing and use of multiple promoters. To address the relationship between mutation of these transcripts and phenotype, we report a three-generation family segregating mild intellectual disability with a chromosomal translocation disruptingTCF4 . Results Using whole genome sequencing, we detected a complex unbalanced karyotype disruptingTCF4 (46, XY, del(14)(q23.3q23.3)del(18)(q21.2q21.2)del(18)(q21.2q21.2)inv(18)(q21.2q21.2)t(14;18)(q23.3;q21.2)(14pter®14q23.3::18q21.2®18q21.2::18q21.1®18qter;18pter®18q21.2::14q23.3®14qter). Subsequent transcriptome sequencing, qRT-PCR and nCounter analyses revealed that cultured skin fibroblasts and peripheral blood had normal expression of genes along chromosomes 14 or 18 and no marked changes in expression of genes other thanTCF4 . Affected individuals had 12–33 fold higher mRNA levels ofTCF4 than did unaffected controls or individuals with PTHS. Although the derivative chromosome generated aPLEKHG3 -TCF4 fusion transcript, the increased levels of TCF4 mRNA arose from transcript variants originating distal to the translocation breakpoint, not from the fusion transcript. Conclusions Although validation in additional patients is required, our findings suggest that the dysmorphic features and severe intellectual disability characteristic of PTHS are partially rescued by overexpression of those shortTCF4 transcripts encoding a nuclear localization signal, a transcription activation domain, and the basic helix-loop-helix domain.