RESUMEN
Mutations in BBS6 cause two clinically distinct syndromes, Bardet-Biedl syndrome (BBS), a syndrome caused by defects in cilia transport and function, as well as McKusick-Kaufman syndrome, a genetic disorder characterized by congenital heart defects. Congenital heart defects are rare in BBS, and McKusick-Kaufman syndrome patients do not develop retinitis pigmentosa. Therefore, the McKusick-Kaufman syndrome allele may highlight cellular functions of BBS6 distinct from the presently understood functions in the cilia. In support, we find that the McKusick-Kaufman syndrome disease-associated allele, BBS6H84Y; A242S, maintains cilia function. We demonstrate that BBS6 is actively transported between the cytoplasm and nucleus, and that BBS6H84Y; A242S, is defective in this transport. We developed a transgenic zebrafish with inducible bbs6 to identify novel binding partners of BBS6, and we find interaction with the SWI/SNF chromatin remodeling protein Smarcc1a (SMARCC1 in humans). We demonstrate that through this interaction, BBS6 modulates the sub-cellular localization of SMARCC1 and find, by transcriptional profiling, similar transcriptional changes following smarcc1a and bbs6 manipulation. Our work identifies a new function for BBS6 in nuclear-cytoplasmic transport, and provides insight into the disease mechanism underlying the congenital heart defects in McKusick-Kaufman syndrome patients.
Asunto(s)
Anomalías Múltiples/genética , Síndrome de Bardet-Biedl/genética , Chaperoninas del Grupo II/genética , Cardiopatías Congénitas/genética , Hidrocolpos/genética , Polidactilia/genética , Factores de Transcripción/genética , Enfermedades Uterinas/genética , Anomalías Múltiples/metabolismo , Anomalías Múltiples/patología , Transporte Activo de Núcleo Celular/genética , Animales , Animales Modificados Genéticamente/genética , Síndrome de Bardet-Biedl/metabolismo , Síndrome de Bardet-Biedl/patología , Cromatina/genética , Ensamble y Desensamble de Cromatina/genética , Cilios/metabolismo , Cilios/patología , Citoplasma/metabolismo , Modelos Animales de Enfermedad , Cardiopatías Congénitas/metabolismo , Cardiopatías Congénitas/patología , Humanos , Hidrocolpos/metabolismo , Hidrocolpos/patología , Ratones , Mutación , Polidactilia/metabolismo , Polidactilia/patología , Transporte de Proteínas/genética , Factores de Transcripción/biosíntesis , Enfermedades Uterinas/metabolismo , Enfermedades Uterinas/patología , Pez Cebra/genéticaRESUMEN
PURPOSE: To identify the causative mutation in two siblings from a consanguineous family in India with retinitis pigmentosa (RP) and polydactyly without other findings of Bardet-Biedl syndrome (BBS). We also performed functional characterization of the mutant protein to explore its role in this limited form of BBS. METHODS: The siblings underwent a thorough ophthalmological examination, including retinal optical coherence tomography (OCT) imaging, and an extensive physical examination with abdominal ultrasonography to characterize the disease phenotype. Next-generation sequencing (NGS) using a panel targeting retinal degeneration genes was performed on genomic DNA samples from the siblings and parents. Upon identification of the causative mutation, functional characterization was accomplished by performing protein-protein interaction studies in human embryonic kidney (HEK-293T) and human adult retinal pigmented epithelium (ARPE-19) cells. RESULTS: The two siblings showed signs of RP and polydactyly. The patients did not have truncal obesity, renal anomalies, hydrometrocolpos, congenital heart disease, or overt cognitive defects. NGS identified a homozygous c.1184A>G mutation in the MKKS/BBS6 gene in both patients resulting in a p.H395R substitution in the MKKS/BBS6 protein. This mutant protein decreased the interaction of MKKS/BBS6 with BBS12 but did so to a different extent in the HEK-293T versus ARPE-19 cells. Nonetheless, the effect of the H395R variant on disrupting interactions with BBS12 was not as profound as other reported MKKS/BBS6 mutations associated with syndromic RP. CONCLUSIONS: We identified a novel H395R substitution in MKKS/BBS6 that results in a unique phenotype of only RP and polydactyly. Our observations reaffirm the notion that mutations in MKKS/BBS6 cause phenotypic heterogeneity and do not always result in classic MKKS or BBS findings.
Asunto(s)
Anomalías Múltiples/genética , Síndrome de Bardet-Biedl/genética , Chaperoninas del Grupo II/genética , Cardiopatías Congénitas/genética , Hidrocolpos/genética , Mutación Missense , Polidactilia/genética , Retinitis Pigmentosa/genética , Enfermedades Uterinas/genética , Adolescente , Western Blotting , Consanguinidad , Análisis Mutacional de ADN , Femenino , Células HEK293 , Secuenciación de Nucleótidos de Alto Rendimiento , Humanos , Masculino , Linaje , Plásmidos , Epitelio Pigmentado de la Retina/citología , Hermanos , Tomografía de Coherencia ÓpticaRESUMEN
BACKGROUND: Upstream open reading frames (uORFs) are commonly found in the 5'-untranslated region (UTR) of many genes and function in translational control. However, little is known about the existence of the proteins encoded by uORFs, and the role of the proteins except translational control. There was no report about uORFs of the McKusick-Kaufman syndrome (MKKS) gene that causes a genetic disorder. METHODS: Northern blotting, 3'-RACE, and bioinformatics were used for determining the length of transcripts and their 3' ends. Luciferase assay and in vitro translation were used for evaluation of translational regulatory activity of uORFs. Immunoblotting and immunocytochemical analyses were used for detection of uORF-derived protein products and their subcellular localization. RESULTS: The MKKS gene generates two types of transcripts: a canonical long transcript that encodes both uORFs and MKKS, and a short transcript that encodes only uORFs by using alternative polyadenylation sites at the 5'-UTR. The simultaneous disruption of the uORF initiation codons increased the translation of the downstream ORF. Furthermore, both protein products from the two longest uORFs were detected in the mitochondrial membrane fraction of HeLa cells. Database searches indicated that such uORFs with active alternative polyadenylation sites at the 5'-UTR are atypical but surely exist in human transcripts. CONCLUSIONS: Multiple uORFs at the 5'-UTR of the MKKS long transcript function as translational repressor for MKKS. Two uORFs are translated in vivo and imported onto the mitochondrial membrane. GENERAL SIGNIFICANCE: Our findings provide unique insights into production of uORF-derived peptides and functions of uORFs.
Asunto(s)
Regiones no Traducidas 5' , Anomalías Múltiples/genética , Empalme Alternativo , Cardiopatías Congénitas/genética , Hidrocolpos/genética , Proteínas Mitocondriales/genética , Sistemas de Lectura Abierta , Polidactilia/genética , ARN Mensajero/genética , Enfermedades Uterinas/genética , Anomalías Múltiples/metabolismo , Anomalías Múltiples/patología , Secuencia de Aminoácidos , Animales , Línea Celular Tumoral , Biblioteca de Genes , Genes Reporteros , Haplorrinos , Cardiopatías Congénitas/metabolismo , Cardiopatías Congénitas/patología , Humanos , Hidrocolpos/metabolismo , Hidrocolpos/patología , Luciferasas , Ratones , Mitocondrias/genética , Mitocondrias/metabolismo , Proteínas Mitocondriales/metabolismo , Datos de Secuencia Molecular , Poliadenilación , Polidactilia/metabolismo , Polidactilia/patología , Biosíntesis de Proteínas , ARN Mensajero/metabolismo , Ratas , Alineación de Secuencia , Enfermedades Uterinas/metabolismo , Enfermedades Uterinas/patologíaRESUMEN
Bardet-Biedl syndrome (BBS) is a ciliopathy characterized by retinal degeneration, obesity, polydactyly, renal abnormalities, and cognitive impairment for which 15 causative genes have been identified. Here we present the results of a mutational analysis of our multiethnic cohort of 83 families (105 cases); 75.9% of them have their mutations identified including 26 novel changes. Comprehensive phenotyping of these patients demonstrate that the spectrum of clinical features is greater than expected and overlapped with the features of other ciliopathies; specifically Alström and McKusick-Kauffman syndromes.
Asunto(s)
Síndrome de Bardet-Biedl/clasificación , Síndrome de Bardet-Biedl/diagnóstico , Mutación/genética , Anomalías Múltiples/diagnóstico , Anomalías Múltiples/genética , Anomalías Múltiples/patología , Adolescente , Adulto , Síndrome de Alstrom/diagnóstico , Síndrome de Alstrom/genética , Síndrome de Alstrom/patología , Síndrome de Bardet-Biedl/genética , Niño , Preescolar , Análisis Mutacional de ADN , Etnicidad/genética , Femenino , Estudios de Asociación Genética , Cardiopatías Congénitas/diagnóstico , Cardiopatías Congénitas/genética , Cardiopatías Congénitas/patología , Humanos , Hidrocolpos/diagnóstico , Hidrocolpos/genética , Hidrocolpos/patología , Lactante , Masculino , Persona de Mediana Edad , Polidactilia/diagnóstico , Polidactilia/genética , Polidactilia/patología , Enfermedades Uterinas/diagnóstico , Enfermedades Uterinas/genética , Enfermedades Uterinas/patologíaRESUMEN
Hydrometrocolpos and polydactyly diagnosed in the prenatal period or early childhood may raise diagnostic dilemmas especially in distinguishing McKusick-Kaufman syndrome (MKKS) and the Bardet-Biedl syndrome (BBS). These two conditions can initially overlap. With time, the additional features of BBS appearing in childhood, such as retinitis pigmentosa, obesity, learning disabilities and progressive renal dysfunction allow clear differentiation between BBS and MKKS. Genotype overlap also exists, as mutations in the MKKS-BBS6 gene are found in both syndromes. We report 7 patients diagnosed in the neonatal period with hydrometrocolpos and polydactyly who carry mutations in various BBS genes (BBS6, BBS2, BBS10, BBS8 and BBS12), stressing the importance of wide BBS genotyping in patients with this clinical association for diagnosis, prognosis and genetic counselling.