Asunto(s)
1-Acilglicerol-3-Fosfato O-Aciltransferasa/genética , Eritrodermia Ictiosiforme Congénita/genética , Errores Innatos del Metabolismo Lipídico/genética , Enfermedades Musculares/genética , Mutación , Niño , Exoma , Homocigoto , Humanos , Eritrodermia Ictiosiforme Congénita/diagnóstico , Eritrodermia Ictiosiforme Congénita/patología , Errores Innatos del Metabolismo Lipídico/diagnóstico , Errores Innatos del Metabolismo Lipídico/patología , Masculino , Enfermedades Musculares/diagnóstico , Enfermedades Musculares/patología , Análisis de Secuencia de ADN , Piel/patologíaRESUMEN
Hyperphosphatemic familial tumoral calcinosis (HFTC), secondary to fibroblast growth factor 23 (FGF23) gene mutation, is a rare genetic disorder characterized by recurrent calcified masses. We describe young Lebanese cousins presenting with HFTC, based on a retrospective chart review and a prospective case study. In addition, we present a comprehensive review on the topic, based on a literature search conducted in PubMed and Google Scholar, in 2014 and updated in December 2017. While the patients had the same previously reported FGF23 gene mutation (homozygous c.G367T variant in exon 3 leading to a missense mutation), they presented with variable severity and age of disease onset (at 4 years in patient 1 and at 23 years in patient 2). A review of the literature revealed several potential patho-physiologic pathways of HFTC clinical manifestations, some of which may be independent of hyperphosphatemia. Most available treatment options aim at reducing serum phosphate level, by stimulating renal excretion or by inhibiting intestinal absorption. HFTC is a challenging disease. While the available medical treatment has a limited and inconsistent effect on disease symptomatology, surgical resection of calcified masses remains the last resort. Research is needed to determine the safety and efficacy of FGF23 replacement or molecular therapy, targeting the specific genetic aberration. Hyperphosphatemic familial tumoral calcinosis is a rare genetic disorder characterized by recurrent calcified masses, in addition to other visceral, skeletal, and vascular manifestations. It remains a very challenging disease.
Asunto(s)
Calcinosis/genética , Factores de Crecimiento de Fibroblastos/genética , Hiperostosis Cortical Congénita/genética , Hiperfosfatemia/genética , Mutación , Adolescente , Adulto , Densidad Ósea/genética , Calcinosis/diagnóstico por imagen , Calcinosis/patología , Ecocardiografía , Femenino , Factor-23 de Crecimiento de Fibroblastos , Humanos , Hiperostosis Cortical Congénita/diagnóstico por imagen , Hiperostosis Cortical Congénita/patología , Hiperfosfatemia/diagnóstico por imagen , Hiperfosfatemia/patología , Masculino , Linaje , Estudios Prospectivos , Radiografía , Estudios Retrospectivos , Tomografía Computarizada por Rayos XRESUMEN
Hereditary vitamin D-resistant rickets (HVDRR) is a rare genetic disorder caused by mutations at the level of the vitamin D receptor ( VDR) gene. The disease is characterized by refractory hypocalcemia, elevated serum levels of 1,25-dihydroxy-vitamin D, retarded growth, sparse body hair (sometimes alopecia), premature tooth loss, enlarged pulp chambers, thin dentine, and hypoplastic enamel. The aims of this study were 1) to document the dental development of children with HVDRR in association with the mutation type within the VDR and 2) to evaluate the association between dental development and the timing of and response to HVDRR treatment. Genome analysis was performed for 4 affected children (2 y 2 mo to 6 y 8 mo) under treatment with high doses of vitamin D and calcium. Longitudinal records of clinical and radiographic data on their dental development were assessed in relation to genetic profile and response to treatment. Treatment success depended on the position of the mutation within the VDR protein: children with the p.R391S mutation had a favorable outcome but maintained alopecia totalis, while 1 child with the p.H397P mutation and normal hair had no response to very high doses of vitamin D. The primary incisors, formed prenatally and first to emerge, were missing in 3 children and mobile in 1 child; parents reported loss within months posteruption. Posterior teeth were present, having erupted after treatment initiation. Hypoplastic enamel in emerging teeth was associated with late treatment onset. Mutation type in the VDR gene appears to be related to differences in the disease phenotype and response to treatment. Dental development represents an indicator of the disease process, initially protected by maternal blood levels of calcium and later restored by therapeutic supplies that normalize these levels. Knowledge Transfer Statement: Two novel mutations were associated with different HVDRR phenotypes, one of which responded positively to treatment. Early detection of the mutation should help pediatricians forecast treatment protocol and response. The results also highlight the direct relationship between dental development and blood calcium levels, underscoring the importance of early diagnosis and treatment of HVDRR to minimize the loss of primary teeth and reduce structural abnormalities of permanent teeth.
Asunto(s)
Raquitismo Hipofosfatémico Familiar/genética , Mutación , Odontogénesis/genética , Receptores de Calcitriol/genética , Alopecia/etiología , Calcio/uso terapéutico , Niño , Preescolar , Análisis Mutacional de ADN , Raquitismo Hipofosfatémico Familiar/complicaciones , Raquitismo Hipofosfatémico Familiar/tratamiento farmacológico , Raquitismo Hipofosfatémico Familiar/fisiopatología , Femenino , Humanos , Hipocalcemia/tratamiento farmacológico , Masculino , Odontogénesis/fisiología , Linaje , Fenotipo , Vitamina D/uso terapéutico , Vitaminas/uso terapéuticoRESUMEN
The Wnt signalling pathway is a major pathway involved in the embryogenic development of the various organs of the body. Appropriate signalling in this pathway relies on the proper functioning of several proteins including the R-spondin family of proteins. Deactivating mutations in R-spondin 4 are associated with anonychia. We present the case of a 26-year-old man presenting with anonychia of the 20 nails, which had been present since birth. Using genetic studies, we identified a novel nonsense mutation, c.164-165TC>AA, characterized by two consecutive mismatch bases. To our knowledge, this mutation is the first to be reported in R-spondin 4 in a Lebanese population. Evaluating new patients with anonychia provides fruitful clinical and molecular findings.
Asunto(s)
Codón sin Sentido , Uñas Malformadas/congénito , Trombospondinas/genética , Adulto , Humanos , Masculino , Uñas Malformadas/genéticaRESUMEN
Erythropoietic protoporphyria (EPP) is a rare cutaneous and systemic disease caused by mutations in the ferrochelatase gene (FECH). The molecular underpinnings of EPP in Middle Eastern populations and relative to other ethnic groups secondary to increased consanguinity are unknown. To understand the molecular pathogenesis of Middle Eastern EPP, we surveyed clinicopathological and molecular features in 6 large consanguineous families from Lebanon and Syria presenting with cutaneous and systemic features consistent with EPP. We observed 30% increased liver disease and 20% elevated end-stage liver complications in our EPP cohort compared to EPP patients previously reported elsewhere. In addition, Middle Eastern EPP patients in our cohort exhibited uniquely an increased incidence of colon cancer. Sequence analysis revealed 2 novel non-synonymous FECH mutations in the studied families designated p.M294T and p.I230M. In addition, FECH activity was significantly decreased (6%) in fibroblasts obtained from sun-exposed sites in a patient with p.M294T mutation, whereas in sharp contrast, protected sites from the same patient exhibited 54% activity for the gene. We also found that sun-exposed fibroblasts, relative to sun-protected and control fibroblasts, exhibited suppressed growth and atypical morphology in vitro, and that these effects were alleviated when the cells were co-cultured with sun-protected fibroblasts. Our findings on the increased incidence of colon cancer in EPP patients prompted us to survey FECH expression patterns in cancer. Using publicly available microarray datasets we found that FECH mRNA was largely significantly decreased in colon adenocarcinomas relative to normal colon tissues. Our findings suggest that families with autosomal recessive EPP should be screened more extensively for systemic involvement including liver diseases and colon cancer, and point to a previously unknown yet plausible tumor suppressor role for FECH in colon malignancy.
Asunto(s)
Neoplasias del Colon/enzimología , Neoplasias del Colon/genética , Ferroquelatasa/genética , Genes Supresores de Tumor , Protoporfiria Eritropoyética/enzimología , Protoporfiria Eritropoyética/genética , Adolescente , Secuencia de Bases , Niño , Técnicas de Cocultivo , Consanguinidad , Familia , Femenino , Ferroquelatasa/metabolismo , Fibroblastos/patología , Regulación Neoplásica de la Expresión Génica , Humanos , Líbano , Hepatopatías/complicaciones , Masculino , Mutación Missense/genética , Linaje , Fenotipo , Protoporfiria Eritropoyética/mortalidad , ARN Mensajero/genética , ARN Mensajero/metabolismo , Adulto JovenAsunto(s)
ADN/genética , Genes pX/genética , Hiperqueratosis Epidermolítica/genética , Queratodermia Palmoplantar/genética , Proteínas de la Membrana/metabolismo , Mutación , Niño , Análisis Mutacional de ADN , Femenino , Humanos , Hiperqueratosis Epidermolítica/diagnóstico , Hiperqueratosis Epidermolítica/metabolismo , Irak , Queratodermia Palmoplantar/diagnóstico , Queratodermia Palmoplantar/metabolismo , LinajeRESUMEN
Solute carrier family 22 member 5 (SLC22A5) encodes a sodium-dependent ion transporter responsible for shuffling carnitine across the plasma membrane. This process provides energy for the heart, among other organs allowing beta-oxidation of fatty acids. Mutations in SLC22A5 result in primary carnitine deficiency (PCD), a disorder that manifests with cardiac, skeletal, or metabolic symptoms. We hereby describe two novel mutations in SLC22A5 in two Lebanese families associated exclusively with a cardiac phenotype. The frequency of the cardiac, metabolic and skeletal symptoms in PCD patients remains undefined. All the reported eight PCD patients belonging to five different Lebanese families have an exclusive cardiac phenotype. Carnitine levels appear to be directly linked to the type and position of the mutation and the severity of the phenotypic presentation does not seem to be associated with serum carnitine levels. A comprehensive review of 61 literature-reported PCD cases revealed an exclusive cardiac manifestation frequency at 62.3% with a very low likelihood of simultaneous occurrence of cardiac and metabolic manifestation.
Asunto(s)
Cardiomiopatías/genética , Cardiomiopatía Dilatada/genética , Carnitina/deficiencia , Hiperamonemia/genética , Enfermedades Musculares/genética , Miocardio/patología , Proteínas de Transporte de Catión Orgánico/genética , Fenotipo , Secuencia de Bases , Cardiomiopatías/patología , Cardiomiopatía Dilatada/patología , Carnitina/genética , Niño , Preescolar , Codón sin Sentido/genética , Cartilla de ADN/genética , Ecocardiografía , Femenino , Humanos , Hiperamonemia/patología , Lactante , Líbano , Modelos Logísticos , Masculino , Datos de Secuencia Molecular , Enfermedades Musculares/patología , Oportunidad Relativa , Linaje , Reacción en Cadena de la Polimerasa , Análisis de Secuencia de ADN , Eliminación de Secuencia/genética , Miembro 5 de la Familia 22 de Transportadores de SolutosAsunto(s)
Cardiomiopatía Dilatada/genética , Carnitina/deficiencia , Secuencia de Bases , Cardiomiopatía Dilatada/fisiopatología , Niño , Preescolar , Codón sin Sentido , ADN Complementario/genética , Exones , Femenino , Genes Recesivos , Genotipo , Humanos , Lactante , Líbano , Errores Innatos del Metabolismo Lipídico/genética , Errores Innatos del Metabolismo Lipídico/fisiopatología , Masculino , Proteínas de Transporte de Catión Orgánico/genética , Linaje , Fenotipo , Miembro 5 de la Familia 22 de Transportadores de Solutos , Disfunción Ventricular Izquierda/genética , Disfunción Ventricular Izquierda/fisiopatologíaRESUMEN
Heterozygous Tbx5(del/+) mice were generated to study the mechanisms by which TBX5 haploinsufficiency causes cardiac and forelimb abnormalities seen in Holt-Oram syndrome. Tbx5 deficiency in homozygous mice (Tbx5(del/del)) decreased expression of multiple genes and caused severe hypoplasia of posterior domains in the developing heart. Surprisingly, Tbx5 haploinsufficiency also markedly decreased atrial natriuretic factor (ANF) and connexin 40 (cx40) transcription, implicating these as Tbx5 target genes and providing a mechanism by which 50% reduction of T-box transcription factors cause disease. Direct and cooperative transactivation of the ANF and cx40 promoters by Tbx5 and the homeodomain transcription factor Nkx2-5 was also demonstrated. These studies provide one potential explanation for Holt-Oram syndrome conduction system defects, suggest mechanisms for intrafamilial phenotypic variability, and account for related cardiac malformations caused by other transcription factor mutations.
Asunto(s)
Anomalías Múltiples/genética , Factor Natriurético Atrial/genética , Desarrollo Óseo/fisiología , Cardiopatías Congénitas/genética , Proteínas de Dominio T Box/genética , Envejecimiento , Animales , Secuencia de Bases , Sitios de Unión , Desarrollo Óseo/genética , Diferenciación Celular , Conexinas/genética , Modelos Animales de Enfermedad , Electrocardiografía , Desarrollo Embrionario y Fetal , Miembro Anterior/anomalías , Corazón/embriología , Cardiopatías Congénitas/fisiopatología , Heterocigoto , Homocigoto , Humanos , Ratones , Ratones Noqueados , Datos de Secuencia Molecular , Miocardio/citología , Regiones Promotoras Genéticas , Ratas , Alineación de Secuencia , Homología de Secuencia de Ácido Nucleico , Ovinos , Síndrome , Proteínas de Dominio T Box/deficiencia , Proteína alfa-5 de Unión ComunicanteRESUMEN
Understanding the molecular mechanisms controlling cardiac-specific gene transcription requires the dissection of the cis-elements that govern the complex spatio-temporal expression of these genes. The four-chambered vertebrate heart is formed during the late phases of fetal development following a series of complex morphogenetic events that require the functional presence of different proteins. The gradient-like expression of some genes, as well as the chamber-specific expression of others, is tightly regulated by combinatorial interactions of several transcription factors and their cofactors. Chamber- and stage-specific cardiac myocyte cultures have been invaluable for identifying transcription factor binding sites involved in basal, chamber-specific, and inducible expression of many cardiac promoters; these studies, which were largely confirmed in vivo in transgenic mouse models, led to the isolation of key regulators of heart development. In addition, the use of pluripotent embryonic stem cells helped elucidate the early molecular events controlling cardiomyocyte differentiation. Together, these studies point to a major role for GATA transcription factors and their interacting partners in transcriptional control of heart development. In addition, members of the T-box family of transcription factors and homeodomain containing proteins, together with chamber-restricted transcriptional repressors and co-repressors play critical roles in heart septation and chamber specification. These fine-tuned cooperative interactions between different classes of proteins are at the basis of normal cardiac function, and alteration in their expression level or function leads to cardiac pathologies.
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Regulación de la Expresión Génica , Corazón/embriología , Factores de Transcripción/fisiología , Proteínas de Xenopus , Animales , Factor Natriurético Atrial/fisiología , Proteínas de Unión al ADN/fisiología , Factor de Transcripción GATA4 , Proteína Homeótica Nkx-2.5 , Proteínas de Homeodominio/fisiología , Humanos , Factores de Transcripción MEF2 , Factores Reguladores Miogénicos , Fosforilación , Regiones Promotoras Genéticas , Proteínas de Dominio T Box/fisiologíaRESUMEN
The GATA family of zinc finger proteins are transcriptional regulators with critical functions in lineage differentiation and embryonic development. Based on structural and expression pattern comparisons, the GATA proteins have been subdivided into two groups. The first subgroup consists of GATA-1, -2, and -3, which are all highly expressed in the hematopoietic system, whereas GATA-4, -5, and -6 are present essentially in the heart and gut. We have isolated and functionally characterized the rat GATA-5 cDNA, which encodes a 45-kDa protein with 71%, 73%, and 97% homology to its amphibian, avian, and murine homologs, respectively. Northern blot analysis showed that rat GATA-5 is expressed in a dynamic pattern during embryonic and postnatal development. In the midgestation embryo, GATA-5 transcripts are most abundant in the heart and decrease dramatically in the postnatal heart; in contrast, GATA-5 expression is upregulated in the lung and gut during postnatal development. Functional studies with recombinant GATA-4, -5, and -6 proteins show that GATA-5 has preferential affinity for a subset of GATA elements found on cardiac promoters and differentially activate cardiac gene transcription. Structure-function analysis revealed the presence of an activation domain within the carboxy terminal region of GATA-5 that is essential for transcriptional regulation of target promoters. Linkage analysis localized Gata5 to distal mouse Chromosome (Chr) 2 in a conserved linkage group with genes localized to rat Chr 3q43 and human Chr 20q13.2-q13.3. The results suggest that GATA-5 may have specific downstream targets and that GATA-4, -5, and -6 can only partially substitute for each other in cardiogenesis. Thus, Gata5 probably plays a specialized evolutionary conserved role in cardiac development.
Asunto(s)
Mapeo Cromosómico , Proteínas de Unión al ADN/genética , Factores de Transcripción/genética , Secuencia de Aminoácidos , Animales , Diferenciación Celular/genética , Línea Celular , Cromosomas Humanos Par 20 , Clonación Molecular , Proteínas de Unión al ADN/química , Factor de Transcripción GATA5 , Regulación del Desarrollo de la Expresión Génica , Ligamiento Genético , Humanos , Ratones , Datos de Secuencia Molecular , Miocardio/metabolismo , ARN Mensajero/metabolismo , Ratas , Ratas Sprague-Dawley , Proteínas Recombinantes , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Homología de Secuencia de Aminoácido , Factores de Transcripción/química , Activación Transcripcional , Dedos de Zinc/genéticaRESUMEN
Two members of the GATA family of transcription factors, GATA-4 and GATA-6, are expressed in the developing and postnatal myocardium and are equally potent transactivators of several cardiac promoters. However, several in vitro and in vivo lines of evidence suggest distinct roles for the two factors in the heart. Since identification of the endogenous downstream targets of GATA factors would greatly help to elucidate their exact functions, we have developed an adenovirus-mediated antisense strategy to specifically inhibit GATA-4 and GATA-6 protein production in postnatal cardiomyocytes. Expression of several endogenous cardiac genes was significantly down-regulated in cells lacking GATA-4 or GATA-6, indicating that these factors are required for the maintenance of the cardiac genetic program. Interestingly, transcription of some genes like the alpha- and beta-myosin heavy-chain (alpha- and beta-MHC) genes was preferentially regulated by GATA-4 due, in part, to higher affinity of GATA-4 for their promoter GATA element. However, transcription of several other genes, including the atrial natriuretic factor and B-type natriuretic peptide (ANF and BNP) genes, was similarly down-regulated in cardiomyocytes lacking one or both GATA factors, suggesting that GATA-4 and GATA-6 could act through the same transcriptional pathway. Consistent with this, GATA-4 and GATA-6 were found to colocalize in postnatal cardiomyocytes and to interact functionally and physically to provide cooperative activation of the ANF and BNP promoters. The results identify for the first time bona fide in vivo targets for GATA-4 and GATA-6 in the myocardium. The data also show that GATA factors act in concert to regulate distinct subsets of genes, suggesting that combinatorial interactions among GATA factors may differentially control various cellular processes.
Asunto(s)
Proteínas de Unión al ADN/genética , Regulación del Desarrollo de la Expresión Génica , Corazón/crecimiento & desarrollo , Miocardio/metabolismo , Factores de Transcripción/genética , Adenoviridae , Animales , Factor Natriurético Atrial/metabolismo , Northern Blotting , Western Blotting , Células Cultivadas , Reactivos de Enlaces Cruzados/metabolismo , Relación Dosis-Respuesta a Droga , Electroforesis en Gel de Poliacrilamida , Técnica del Anticuerpo Fluorescente , Factor de Transcripción GATA4 , Factor de Transcripción GATA6 , Células HeLa , Atrios Cardíacos/metabolismo , Ventrículos Cardíacos/metabolismo , Humanos , Cinética , Modelos Genéticos , Oligonucleótidos Antisentido , Plásmidos , Ratas , Ratas Sprague-Dawley , Factores de Tiempo , Transfección , beta-Galactosidasa/metabolismoRESUMEN
GATA-4 is a cardiac-specific member of the GATA family of zinc finger transcription factors. During embryogenesis, GATA-4 expression is detected very early in the cardiogenic area and persists later in the developing heart. Studies have shown that GATA-4 is a potent transcriptional activator of several cardiac muscle-specific genes and a key regulator of the cardiomyocyte gene program. Consistent with a role for GATA-4 in cardiomyocyte formation, inhibition of GATA-4 expression by antisense transcripts interferes with expression of cardiac muscle genes and blocks development of beating cardiomyocytes in P19 embryonic stem cells. In order to better define the function of GATA-4 in cardiogenesis, we have carried out molecular analysis of early stages of cardiomyocyte differentiation in GATA-4-deficient P19 cell lines and in P19 cells stably overexpressing GATA-4. The results indicate that GATA-4 is not required for either endodermal or mesodermal commitment or for initiation of the cardiac pathway. However, in the absence of GATA-4, differentiation is blocked at the precardiac (cardioblasts) stage and cells are lost through extensive apoptosis. In contrast, ectopic expression of GATA-4 in P19 cells accelerates cardiogenesis and markedly increases (over 10-fold) the number of terminally differentiated beating cardiomyocytes following cell aggregation. Together, these findings suggest that, in addition to its role in activation of the cardiac genetic program, GATA-4 may be the nuclear target of inductive and/or survival factors for precardiac cells.