RESUMEN

PURPOSE: Our goals were to produce a functional recombinant RPE retinal G protein-coupled receptor (RGR) opsin for biochemical studies and to test the efficiency of a lentiviral vector for transgene expression of human RGR. METHODS: A human RGR cDNA was cloned into a replication-defective lentiviral vector, and recombinant hRGR-Lentivirus was prepared for transduction of the ARPE-19, a human retinal pigment epithelium (RPE) cell line, and COS-7 cells. Recombinant RGR expression was detected by Western blot analysis, and functionality of the protein was tested by a [3H]all-trans-retinal binding assay. RESULTS: RGR protein was detected in each cell type after transduction with recombinant virus and was not observed in untreated cells. RGR expression in ARPE-19 cells increased steadily for up to 10 days after transduction and was stable for at least 6 months. The transduced ARPE-19 cells produced approximately 100-fold higher amounts of RGR protein than the transduced COS-7 cells. When cell membranes from the ARPE-19 cells were incubated with [3H]all-trans-retinal, the chromophore bound specifically to the expressed protein. Uptake of [3H]all-trans-retinol into the ARPE-19 cells was followed by specific binding of radiolabeled retinoid to RGR. CONCLUSIONS: Using a Lentivirus-derived gene delivery system, we were able to express high amounts of human RGR protein in the ARPE-19 human RPE cell line. The transduced ARPE-19 cells remain able to process all-trans-retinol, and the expressed protein is capable of binding to the all-trans-retinal chromophore. The Lentivirus-based expression of functional RGR can be used to study RGR in cultured cells and to test in vivo transduction of quiescent RPE cells.

Asunto(s)

Proteínas del Ojo/biosíntesis , VIH/genética , Epitelio Pigmentado Ocular/metabolismo , Receptores de Superficie Celular/biosíntesis , Receptores Acoplados a Proteínas G , Opsinas de Bastones/biosíntesis , Transducción Genética , Animales , Autorradiografía , Western Blotting , Células COS/metabolismo , Bovinos , Células Cultivadas , Virus Defectuosos , Electroforesis en Gel de Poliacrilamida , Proteínas del Ojo/genética , Vectores Genéticos , Técnicas para Inmunoenzimas , Ratones , Ratones Endogámicos C57BL , Microsomas/metabolismo , Receptores de Superficie Celular/genética , Proteínas Recombinantes/biosíntesis , Proteínas Recombinantes/genética , Retinaldehído/metabolismo , Opsinas de Bastones/genética , Vitamina A/metabolismo

RESUMEN

Myotonic dystrophy (DM) is an autosomal dominant disorder characterized by skeletal muscle wasting, myotonia, cardiac arrhythmia, hyperinsulinaemia, mental retardation and ocular cataracts. The genetic defect in DM is a CTG repeat expansion located in the 3' untranslated region of DMPK and 5' of a homeodomain-encoding gene, SIX5 (formerly DMAHP; refs 2-5). There are three mechanisms by which CTG expansion can result in DM. First, repeat expansion may alter the processing or transport of the mutant DMPK mRNA and consequently reduce DMPK levels. Second, CTG expansion may establish a region of heterochromatin 3' of the repeat sequence and decrease SIX5 transcription. Third, toxic effects of the repeat expansion may be intrinsic to the repeated elements at the level of DNA or RNA (refs 10,11). Previous studies have demonstrated that a dose-dependent loss of Dm15 (the mouse DMPK homologue) in mice produces a partial DM phenotype characterized by decreased development of skeletal muscle force and cardiac conduction disorders. To test the role of Six5 loss in DM, we have analysed a strain of mice in which Six5 was deleted. Our results demonstrate that the rate and severity of cataract formation is inversely related to Six5 dosage and is temporally progressive. Six5+/- and Six5-/- mice show increased steady-state levels of the Na+/K+-ATPase alpha-1 subunit and decreased Dm15 mRNA levels. Thus, altered ion homeostasis within the lens may contribute to cataract formation. As ocular cataracts are a characteristic feature of DM, these results demonstrate that decreased SIX5 transcription is important in the aetiology of DM. Our data support the hypothesis that DM is a contiguous gene syndrome associated with the partial loss of both DMPK and SIX5.

Asunto(s)

Catarata/etiología , Catarata/genética , Proteínas de Homeodominio/genética , Proteínas de Homeodominio/metabolismo , Pérdida de Heterocigocidad/genética , Animales , Mapeo Cromosómico , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Mapeo Restrictivo

RESUMEN

Norrie disease is an X-linked recessive disorder characterized by congenital blindness and in some cases mental retardation and deafness.(1) The variability of signs among patients often complicates diagnosis. Signs such as an ocular pseudoglioma, progressive deafness, and mental disturbance are considered classic features.(2) Only one third of patients with Norrie disease have sensorineural deafness, and approximately one half of the affected individuals exhibit mental retardation, often with psychotic features.(3) Histologic analysis has suggested that retinal dysgenesis occurs early in eye development and involves cells in the inner wall of the optic cup.(4) The gene associated with Norrie disease was identified in 1992. (5,6) We report a novel mutation identified in a patient in whom Norrie disease was diagnosed.

Asunto(s)

Ceguera/congénito , Ceguera/genética , Mutación , Secuencia de Bases , Niño , Cromatografía , Codón/genética , Humanos , Masculino , Datos de Secuencia Molecular , Biosíntesis de Proteínas , Síndrome

RESUMEN

The development of vectors and techniques able to transfer potentially therapeutic genetic information to corneal tissues efficiently may have broad clinical applications. Although a variety of vectors have been tested for their ability to transduce corneal tissue, these systems have been ineffective at transducing all cell types or have been associated with a relatively short duration of transgene expression. Towards the implementation of efficient, long-term transgene expression in all corneal cell types, we have studied the ability of a recombinant lentiviral vector, containing the enhanced green fluorescent protein (eGFP), to mediate gene transfer into human corneal tissue in vitro and in situ. Human primary keratocytes, cultured in vitro, were efficiently transduced by a lentiviral vector as determined by fluorescent-activated cell sorting (FACS) and by fluorescent microscopy. Transduction efficiency was found to be dependent upon multiplicity of infection (MOI); 92% of keratocytes were transduced at an MOI of 1000. The proportion of eGFP-positive cells remained unchanged throughout continuous culture for 60 days, indicating stable expression and a lack of selective pressure for or against transduced cells. Human corneal tissue, obtained at the time of penetrating keratoplasty, demonstrated efficient in situ transduction with this vector. Endothelial cells, epithelial cells and stromal keratocytes at the exposed cut edge of the corneal tissue in situ demonstrated eGFP expression. Underlying stromal cells not in direct contact with vector-containing media, were not transduced, implying that virus-cell contact is required for transduction. Transduced corneal tissues expressed eGFP in situ for the life of the corneal button in extended organ culture (60 days). These results imply that lentiviral vectors may prove to be useful tools, able to transduce corneal tissue efficiently, and that transgene expression is temporally stable. Gene Therapy (2000) 7, 196-200.

Asunto(s)

Epitelio Corneal/fisiología , Vectores Genéticos/genética , Lentivirus/genética , Transgenes/genética , Células Cultivadas , Citometría de Flujo , Expresión Génica , Humanos

RESUMEN

PURPOSE: To evaluate the etiology of a unilateral hemangioblastoma noted in a male with a family history remarkable only for spine surgery in the proband's father. METHODS: Genomic DNA was isolated from peripheral blood of family members, and the three exons of the von Hippel-Lindau gene were examined for mutations by direct sequencing. RESULTS: A three base pair (bp) deletion in exon 1 of the VHL gene was found in the father and both sons. This in-frame deletion results in the loss of a phenylalanine residue from the von Hippel-Lindau protein product, at amino acid position 76. CONCLUSION: Genetic screening has confirmed that von Hippel-Lindau syndrome is responsible for the hemangioblastoma in the proband. Magnetic resonance imaging scans performed as a consequence of these results indicated spinal tumors present in the father and tumors present in the cerebellum of the proband's sibling. As close, lifelong follow-up is warranted with this disease, this case demonstrates the value of DNA testing in patients with ocular findings consistent with von Hippel-Lindau disease in the absence of a recognized family history.

Asunto(s)

ADN/análisis , Eliminación de Gen , Genes Supresores de Tumor/genética , Ligasas , Mutación Puntual , Proteínas/genética , Proteínas Supresoras de Tumor , Ubiquitina-Proteína Ligasas , Enfermedad de von Hippel-Lindau/genética , Adolescente , Adulto , Neoplasias Cerebelosas/diagnóstico , Neoplasias Cerebelosas/genética , Neoplasias Cerebelosas/cirugía , Niño , Cartilla de ADN/química , Pruebas Genéticas , Hemangioblastoma/diagnóstico , Hemangioblastoma/genética , Hemangioblastoma/cirugía , Humanos , Coagulación con Láser , Masculino , Linaje , Neoplasias de la Retina/diagnóstico , Neoplasias de la Retina/genética , Neoplasias de la Retina/cirugía , Neoplasias de la Médula Espinal/diagnóstico , Neoplasias de la Médula Espinal/genética , Neoplasias de la Médula Espinal/cirugía , Proteína Supresora de Tumores del Síndrome de Von Hippel-Lindau , Enfermedad de von Hippel-Lindau/complicaciones , Enfermedad de von Hippel-Lindau/diagnóstico

Asunto(s)

Proteínas del Ojo/genética , Ligamiento Genético , Mutación Puntual , Degeneración Retiniana/genética , Cromosoma X , Adulto , Niño , Preescolar , Análisis Mutacional de ADN , Electrorretinografía , Exones , Femenino , Humanos , Masculino , Mutación Missense , Linaje , Fenotipo , Reacción en Cadena de la Polimerasa , Degeneración Retiniana/diagnóstico

RESUMEN

Homeobox genes, first identified in Drosophila, encode transcription factors that regulate embryonic development along the anteroposterior axis of an organism. Vertebrate homeobox genes are described on the basis of their homology to the genes found within the Drosophila Antennapedia and Bithorax homeotic gene complexes. Mammals possess four paralogous homeobox (HOX) gene clusters, HOX A, HOX B, HOX C and HOX D, each located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. We report the characterization of the human HOX D1 gene. This gene consists of two exons, encoding a 328 amino acid protein, separated by an intron of 354 bp. The human HOX D1 protein is one amino acid longer (328 amino acids) than the mouse protein (327 amino acids) and is 82% identical to the mouse HOX D1 homolog. The DNA binding homeodomain region of the human protein exhibits a 97% and 80% identity between mouse Hoxd1 and Drosophila labial homeodomains, respectively. The exon/intron and intron/exon splice junctions are conserved in position between human and mouse genes. Determination of the human HOX D1 gene structure permits the use of PCR based analysis of this gene for the assessment of mutations, for diseases that link to the HOXD cluster (such as Duanes Retraction Syndrome (DRS)), or polymorphisms associated with human variation. Molecular characterization of the HOXD1 gene may also permit analysis of the functional role of this gene in human neurogenisis.

Asunto(s)

Genes Homeobox/genética , Proteínas de Homeodominio/química , Proteínas de Homeodominio/genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Cromosomas Artificiales Bacterianos , Exones , Humanos , Intrones , Ratones , Datos de Secuencia Molecular , Mutación , Neuronas/metabolismo , Reacción en Cadena de la Polimerasa , Polimorfismo Genético , Estructura Terciaria de Proteína , Análisis de Secuencia de ADN , Homología de Secuencia de Aminoácido

RESUMEN

Duane retraction syndrome (DRS) is a congenital eye-movement disorder characterized by a failure of cranial nerve VI (the abducens nerve) to develop normally, resulting in restriction or absence of abduction, restricted adduction, and narrowing of the palpebral fissure and retraction of the globe on attempted adduction. DRS has a prevalence of approximately 0.1% in the general population and accounts for 5% of all strabismus cases. Undiagnosed DRS in children can lead to amblyopia, a permanent uncorrectable loss of vision. A large family with autosomal dominant DRS was examined and tested for genetic linkage. After exclusion of candidate regions previously associated with DRS, a genomewide search with highly polymorphic microsatellite markers was performed, and significant evidence for linkage was obtained at chromosome 2q31 (D2S2314 maximum LOD score 11.73 at maximum recombination fraction. 0). Haplotype analysis places the affected gene in a 17.8-cM region between the markers D2S2330 and D2S364. No recombinants were seen with markers between these two loci. The linked region contains the homeobox D gene cluster. Three of the genes within this cluster, known to participate in hindbrain development, were sequenced in affected and control individuals. Coding sequences for these genes were normal or had genetic alterations unlikely to be responsible for the DRS phenotype. Identifying the gene responsible for DRS may lead to an improved understanding of early cranial-nerve development.

Asunto(s)

Mapeo Cromosómico , Cromosomas Humanos Par 2/genética , Síndrome de Retracción de Duane/genética , Sustitución de Aminoácidos , Codón/genética , Análisis Mutacional de ADN , Síndrome de Retracción de Duane/fisiopatología , Femenino , Genes Dominantes/genética , Genes Homeobox/genética , Genotipo , Haplotipos , Humanos , Escala de Lod , Masculino , México , Repeticiones de Microsatélite/genética , Mutación/genética , Linaje , Penetrancia

RESUMEN

PURPOSE: To report preliminary linkage analysis of a large Hispanic family showing autosomal dominant inheritance for Duane retraction syndrome. METHODS: Microsatellite analysis was used to examine genomic DNA isolated from members of a large family with autosomal dominant Duane retraction syndrome for linkage to candidate loci for Duane retraction syndrome. Chromosomes 4, 8, and 22 were chosen for study because previous reports had documented karyotypic abnormalities in unrelated patients with Duane retraction syndrome. RESULTS: No lod scores over 0.5 were found for markers on chromosomes 4, 8, or 22. This analysis excludes these candidate sites. CONCLUSIONS: Studies do not support linkage between Duane retraction syndrome in this family and chromosomes 4, 8, and 22. Duane retraction syndrome may result from mutations in a heterogeneous group of genes.

Asunto(s)

ADN/análisis , Síndrome de Retracción de Duane/genética , Repeticiones de Microsatélite/genética , Cromosomas Humanos Par 22/genética , Cromosomas Humanos Par 4/genética , Cromosomas Humanos Par 8/genética , Femenino , Ligamiento Genético , Humanos , Masculino , Linaje

RESUMEN

The sequences of the blue cone photopigments in the talapoin monkey (Miopithecus talapoin), an Old World primate, and in the marmoset (Callithrix jacchus), a New World monkey, are presented. Both genes are composed of 5 exons separated by 4 introns. In this respect, they are identical to the human blue gene, and intron sizes are also similar. Based on the level of amino acid identity, both monkey pigments are members of the S branch of pigments. Alignment of these sequences with the human gene requires the insertion/deletion of two separate codons in exon 1. The silent site divergence between these primate blue genes indicates a separation of the Old and New World primate lineages around 43 million years ago.

Asunto(s)

Evolución Biológica , Callithrix/genética , Cercopithecidae/genética , Proteínas del Ojo/genética , Pigmentos Retinianos/genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Cartilla de ADN/genética , Exones , Humanos , Intrones , Datos de Secuencia Molecular , Opsinas de Bastones , Homología de Secuencia de Aminoácido , Especificidad de la Especie , Factores de Tiempo

RESUMEN

Blue cone pigment (BCP) is one of three types of cone photoreceptors responsible for normal colour vision. In this study, the BCP gene has been localised to chromosome 7q31.3-32 by fluorescent in situ hybridisation of cosmid clones containing the gene. This is consistent with previous mapping of the BCP gene to chromosome 7q31-35.

Asunto(s)

Cromosomas Humanos Par 7 , Ligamiento Genético/genética , Células Fotorreceptoras Retinianas Conos , Pigmentos Retinianos/genética , Células Cultivadas , Mapeo Cromosómico , Percepción de Color , Sondas de ADN , Humanos , Hibridación Fluorescente in Situ , Linfocitos , Oligonucleótidos/química , Reacción en Cadena de la Polimerasa

RESUMEN

The human gene for phosphatidylinositol transfer protein (PITPN) has previously been shown to share sequence and functional homology to part of the Drosophila retinal degeneration B gene (rdgB). In view of the possible involvement of the PITPN locus in the etiology of retinal disease, the gene has been mapped to human chromosome 17p13.3 and mouse Chromosome 11.

Asunto(s)

Proteínas Portadoras/genética , Cromosomas Humanos Par 17 , Drosophila/genética , Proteínas de la Membrana , Degeneración Retiniana/genética , Homología de Secuencia de Aminoácido , Animales , Secuencia de Bases , Mapeo Cromosómico , Humanos , Ratones , Datos de Secuencia Molecular , Proteínas de Transferencia de Fosfolípidos , Polimorfismo de Longitud del Fragmento de Restricción