Tawamie Hasan, Martianov Igor, Wohlfahrt Natalie, Buchert Rebecca, Mengus Gabrielle, Uebe Steffen, Janiri Luigi, Hirsch Franz Wolfgang, Schumacher Johannes, Ferrazzi Fulvia, Sticht Heinrich, Reis André, Davidson Irwin, Colombo Roberto, Abou Jamra Rami
Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany; Institute of Human Genetics, University Medical Center Leipzig, 04103 Leipzig, Germany.
Institut de Génétique et de Biologie Moléculaire et Cellulaire, 67404 Illkirch Cedex, France.
Am J Hum Genet. 2017 Mar 2;100(3):555-561. doi: 10.1016/j.ajhg.2017.01.032.
In two independent consanguineous families each with two children affected by mild intellectual disability and microcephaly, we identified two homozygous missense variants (c.119T>A [p.Met40Lys] and c.92T>A [p.Leu31His]) in TATA-box-binding-protein-associated factor 13 (TAF13). Molecular modeling suggested a pathogenic effect of both variants through disruption of the interaction between TAF13 and TAF11. These two proteins form a histone-like heterodimer that is essential for their recruitment into the general RNA polymerase II transcription factor IID (TFIID) complex. Co-immunoprecipitation in HeLa cells transfected with plasmids encoding TAF11 and TAF13 revealed that both variants indeed impaired formation of the TAF13-TAF11 heterodimer, thus confirming the protein modeling analysis. To further understand the functional role of TAF13, we performed RNA sequencing of neuroblastoma cell lines upon TAF13 knockdown. The transcriptional profile showed significant deregulation of gene expression patterns with an emphasis on genes related to neuronal and skeletal functions and those containing E-box motives in their promoters. Here, we expand the spectrum of TAF-associated phenotypes and highlight the importance of TAF13 in neuronal functions.
在两个独立的近亲家庭中,每个家庭都有两个孩子患有轻度智力残疾和小头畸形,我们在TATA盒结合蛋白相关因子13(TAF13)中鉴定出两个纯合错义变体(c.119T>A [p.Met40Lys] 和c.92T>A [p.Leu31His])。分子建模表明,这两个变体通过破坏TAF13与TAF11之间的相互作用而具有致病作用。这两种蛋白质形成一种组蛋白样异二聚体,这对于它们被招募到通用RNA聚合酶II转录因子IID(TFIID)复合物中至关重要。在转染了编码TAF11和TAF13质粒的HeLa细胞中进行共免疫沉淀,结果表明这两个变体确实损害了TAF13-TAF11异二聚体的形成,从而证实了蛋白质建模分析。为了进一步了解TAF13的功能作用,我们在敲低TAF13后对神经母细胞瘤细胞系进行了RNA测序。转录谱显示基因表达模式存在明显失调,重点是与神经元和骨骼功能相关的基因以及那些启动子中含有E盒基序的基因。在这里,我们扩展了TAF相关表型的范围,并强调了TAF13在神经元功能中的重要性。