An example of parenchymal renal sparing in the context of complex malformations due to a novel mutation in the PBX1 gene. Issue 12 (25th June 2022)

• Record Type: Journal Article
• Authors: Ruscitti, Federica; Cerminara, Maria; Iascone, Maria; Pezzoli, Laura; Rosti, Giulia; Romano, Ferruccio; Ronchetto, Patrizia; Martucciello, Giuseppe; Buratti, Silvia; Buffelli, Francesca; Bocciardi, Renata; Puliti, Aldamaria; Divizia, Maria Teresa
• Is Part Of: Birth defects research. Volume 114:Issue 12(2022)
• Page Start: 674
• Page End: 681
• Publication Date: 2022-06-25
• Subjects: CAKUT -- development -- homeodomain -- kidney -- PBX1 -- WES; Teratology -- Periodicals; Abnormalities, Human -- Periodicals; Congenital Abnormalities; Embryo, Mammalian -- abnormalities; Teratology; Abnormalities, Human; Teratology; Periodicals; Periodicals; 616.043
• DOI: 10.1002/bdr2.2065
• Languages: English
• ISSNs: 2472-1727

Abstract

Abstract: Introduction: PBX1 encodes the pre‐B cell leukemia factor 1, a Three Amino acid Loop Extension (TALE) transcription factor crucial to regulate basic developmental processes. PBX1 loss‐of‐function variants have been initially described in association with renal malformations in both isolated and syndromic forms. Case report: Herein, we report a male infant presenting multiple organ malformations (cleidosternal dysostosis, micrognathia, left lung hypoplasia, wide interatrial defect, pulmonary hypertension, total anomalous pulmonary venous return, intestinal malrotation) and carrying the heterozygous de novo c.868C > T (p.Arg290Trp) variant in PBX1 . This novel variant affects the highly conserved homeodomain of the protein, leading to a non‐conservative substitution and consequently altering its tridimensional structure and DNA‐binding capacity. Conclusion: So far, PBX1 has been reported in association with a broad spectrum of renal anomalies. However, given the role of this gene in many different developing processes, whole‐exome sequencing can detect mutations in PBX1 even in patients with different phenotypes, not necessarily involving the renal primordium. This report presents a novel PBX1 variant with a predicted strong deleterious effect. The mutation leads to a non‐conservative substitution in a very highly conserved domain of the protein, thus altering its tertiary structure and DNA‐binding capacity.