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1.
Hear Res ; 230(1-2): 9-16, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17493778

ABSTRACT

Usher syndrome type 3 is caused by mutations in the USH3A gene, which encodes the protein clarin-1. Clarin-1 is a member of the tetraspanin superfamily (TM4SF) of transmembrane proteins, expressed in the organ of Corti and spiral ganglion cells of the mouse ear. We have examined whether the AAV-mediated anti-clarin ribozyme delivery causes apoptotic cell death in vivo in the organ of Corti. We used an AAV-2 vector delivered hammerhead ribozyme, AAV-CBA-Rz, which specifically recognizes and cleaves wild type mouse clarin-1 mRNA. Cochleae of CD-1 mice were injected either with 1mul of the AAV-CBA-Rz, or control AAV vectors containing the green fluorescent protein (GFP) marker gene (AAV-CBA-GFP). Additional controls were performed with saline only. At one-week and one-month post-injection, the animals were sacrificed and the cochleae were studied by histology and fluorescence imaging. Mice injected with AAV-CBA-GFP displayed GFP reporter expression of varying fluorescence intensity throughout the length of the cochlea in the outer and inner hair cells and stria vascularis, and to a lesser extent, in vestibular epithelial cells. GFP expression was not detectable in the spiral ganglion. The pro-apoptotic effect of AAV-CBA-delivered anti-clarin-1 ribozymes was evaluated by TUNEL-staining. We observed in the AAV-CBA-Rz, AAV-CBA-GFP and saline control groups apoptotic nuclei in the outer and inner hair cells and in the stria vascularis one week after the microinjection. The vestibular epithelium was also observed to contain apoptotic cells. No TUNEL-positive spiral ganglion neurons were detected. After one-month post-injection, the AAV-CBA-Rz-injected group had significantly more apoptotic outer and inner hair cells and cells of the stria vascularis than the AAV-CBA-GFP group. In this study, we demonstrate that AAV-CBA mediated clarin-1 ribozyme may induce apoptosis of the cochlear hair cells and cells of the stria vascularis. Surprisingly, we did not observe apoptosis in spiral ganglion cells, which should also be susceptible to clarin-1 mRNA cleavage. This result may be due to the injection technique, the promoter used, or tropism of the AAV serotype 2 viral vector. These results suggest the role of apoptosis in the progression of USH3A hearing loss warrants further evaluation.


Subject(s)
Apoptosis , Cochlea/pathology , Dependovirus/genetics , Gene Transfer Techniques , Genetic Vectors , Membrane Proteins/metabolism , RNA, Catalytic/metabolism , Usher Syndromes/pathology , Animals , Cochlea/metabolism , Genes, Reporter , Green Fluorescent Proteins , Hair Cells, Auditory/metabolism , Hair Cells, Auditory/pathology , In Situ Nick-End Labeling , Male , Membrane Proteins/genetics , Mice , Microscopy, Fluorescence , RNA, Messenger/metabolism , Stria Vascularis/metabolism , Stria Vascularis/pathology , Time Factors , Usher Syndromes/genetics , Usher Syndromes/metabolism
2.
J Med Genet ; 43(8): 699-704, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16505158

ABSTRACT

BACKGROUND: X linked cone-rod dystrophy (CORDX) is a recessive retinal disease characterised by progressive dysfunction of photoreceptors. It is genetically heterogeneous, showing linkage to three X chromosomal loci. CORDX1 is caused by mutations in the RPGR gene (Xp21.1), CORDX2 is located on Xq27.2-28, and we recently localised CORDX3 to Xp11.4-q13.1. We aimed to identify the causative gene behind the CORDX3 phenotype. METHODS: All 48 exons of the CACNA1F gene were screened for mutations by DNA sequencing. RNA from cultured lymphoblasts and peripheral blood activated T lymphocytes was analysed by RT-PCR and sequencing. RESULTS: A novel CACNA1F mutation, IVS28-1 GCGTC>TGG, in the splice acceptor site of intron 28 was identified. Messenger RNA studies indicated that the identified mutation leads to altered splicing of the CACNA1F transcript. Aberrant splice variants are predicted to result in premature termination and deletions of the encoded protein, Ca(v)1.4 alpha1 subunit. CONCLUSION: CACNA1F mutations cause the retinal disorder, incomplete congenital stationary night blindness (CSNB2), although mutations have also been detected in patients with divergent diagnoses. Our results indicate that yet another phenotype, CORDX3, is caused by a mutation in CACNA1F. Clinically, CORDX3 shares some features with CSNB2 but is distinguishable from CSNB2 in that it is progressive, can begin in adulthood, has no nystagmus or hyperopic refraction, has only low grade astigmatism, and in dark adaptation lacks cone threshold and has small or no elevation of rod threshold. Considering all features, CORDX3 is more similar to other X chromosomal cone-rod dystrophies than to CSNB2.


Subject(s)
Calcium Channels, L-Type/genetics , Genetic Diseases, X-Linked/genetics , Mutation/genetics , Retinitis Pigmentosa/genetics , Adult , Case-Control Studies , Child , DNA Mutational Analysis , Exons/genetics , Female , Humans , Male , RNA, Messenger/genetics , RNA, Messenger/metabolism
3.
Brain Res Dev Brain Res ; 118(1-2): 1-11, 1999 Dec 10.
Article in English | MEDLINE | ID: mdl-10611498

ABSTRACT

Deficiency in palmitoyl protein thioesterase (PPT) results in the rapid death of neocortical neurons in human. Very little is known about the developmental and cell-specific expression of this lysosomal enzyme. Here we show that PPT is expressed as a major 2.65 kb and a minor 1.85 kb transcript in the mouse brain. Transcript levels gradually increase between postnatal days 10 and 30. In situ hybridization analysis revealed that PPT transcripts are found widely but not homogeneously in the brain. The most intense signal was detected in the cerebral cortex (layers II, IV-V), hippocampal CA1-CA3 pyramidal cells, dentate gyrus granule cells and the hypothalamus. Immunostaining of PPT was localized in the cell soma, axons and dendrites, especially in the pyramidal and granular cells of the hippocampus, correlating well, both spatially and temporally, with the immunoreactivity of a presynaptic vesicle membrane protein, synaptophysin. In whole embryos, at embryonic day 8, the PPT mRNA expression was most apparent throughout the neuroepithelium, and from day 9 onwards it was seen in all tissues. The expression pattern of PPT suggests its general significance for the brain cells and reflects the response to maturation and growth of the neural networks. Strong PPT immunoreactivity in the axons and dentrites would imply that PPT may not be exclusively a lysosomal enzyme. A notable correlation with synaptophysin would suggest that PPT may have a role in the function of the synaptic machinery.


Subject(s)
Aging/metabolism , Animals, Newborn/metabolism , Brain/embryology , Brain/metabolism , Fetus/metabolism , Thiolester Hydrolases/metabolism , Animals , Animals, Newborn/growth & development , Embryonic and Fetal Development , Fetus/physiology , Immunohistochemistry , In Situ Hybridization , Mice , Mice, Inbred Strains , RNA, Messenger/metabolism , Reference Values , Thiolester Hydrolases/genetics , Tissue Distribution
4.
Prenat Diagn ; 19(7): 685-8, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10419622

ABSTRACT

The first prenatal diagnosis of variant late infantile neuronal ceroid lipofuscinosis (vLINCL[Finnish]; CLN5) is reported. The disease belongs to the group of progressive encephalopathies in children with psycho-motor deterioration, visual failure and premature death. Neurons and several extraneural cells harbour lysosomal inclusions showing accumulation of material with histochemical characteristics of ceroid and lipofuscin. A Finnish woman with a daughter with vLINCL came for genetic counselling for her current pregnancy. Electron microscopy of a chorionic villus sample (CVS) at the 11th week of gestation did not reveal inclusions characteristic for NCL. DNA analysis showed that the fetus had inherited the major mutation, a 2 bp deletion of the CLN5 gene from the mother, and the same paternal (and maternal) haplotypes for COLAC1 and AC224 as the affected daughter. The pregnancy was terminated. Electron microscopy of the CVS of the aborted fetus at the 14th week of pregnancy showed lysosomal electron dense inclusions with straight and curved lamellar profiles consistent with vLINCL. Prenatal diagnosis of NCL-disorders (CLN1, CLN2, CLN3) can be made from CVS by demonstrating the mutations of the affected genes or by haplotype analysis using the closely linked markers in most cases. In various clinical settings the DNA diagnostics may not be possible. Demonstration of the characteristic inclusions of the placenta and fetal tissues remains a helpful adjunct in such cases.


Subject(s)
Neuronal Ceroid-Lipofuscinoses/diagnosis , Prenatal Diagnosis , Child , Chorionic Villi Sampling , DNA Mutational Analysis , Female , Gene Deletion , Gestational Age , Haplotypes , Humans , Lysosomal Membrane Proteins , Membrane Proteins/genetics , Microscopy, Electron , Mutation , Neuronal Ceroid-Lipofuscinoses/genetics , Neuronal Ceroid-Lipofuscinoses/pathology , Pregnancy , Tripeptidyl-Peptidase 1
5.
Mol Genet Metab ; 66(4): 324-8, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10191122

ABSTRACT

Neuronal ceroid lipofuscinoses (NCLs) in children are progressive encephalopathies inherited as autosomal recessive traits. Progressive neuronal damage leads to psychomotor deterioration, visual failure, seizures, and finally to premature death. Based on the clinical course of the disease, the childhood forms can be divided into several subtypes. A variant form of the late infantile NCL (vLINCL), characterized by mental retardation, visual failure, ataxia, myoclonia, and death between the ages of 13 and 30 years, is prevalent in Finland. Information on ancient recombination events in disease alleles rising from this isolated population provided an efficient tool for refining the initial assignment of the CLN5 locus. Here we describe the steps resulting in the identification of the novel gene, defective in vLINCL.


Subject(s)
Membrane Proteins/genetics , Neuronal Ceroid-Lipofuscinoses/genetics , Blotting, Northern , Chromosome Mapping , Chromosomes, Human, Pair 13 , Codon, Terminator , DNA Mutational Analysis , Founder Effect , Gene Deletion , Humans , In Situ Hybridization, Fluorescence , Lysosomal Membrane Proteins , Models, Genetic , Pedigree , Physical Chromosome Mapping , Tissue Distribution
6.
Genomics ; 44(3): 355-7, 1997 Sep 15.
Article in English | MEDLINE | ID: mdl-9325059

ABSTRACT

Chromosome 13 is one of the poorly mapped human chromosomes. As an example, only two cloned genes have been assigned to bands 13q22-q31. Our characterization of the critical region for the variant form of late infantile neuronal ceroid lipofuscinosis (vLINCL, locus definition CLN5) disease region on 13q22 resulted in the identification of the sequences encoding the BTF3 protein homologue gene (HGMW-approved symbol BTF3) and a novel pseudogene for RNA Helicase A (HGMW-approved symbol DDX9P). Precise visual assignment to the physical clones covering this region and the positional relationships of these genes were achieved by the use of tyramine enhancement of Fiber-FISH hybridization signals, demonstrating the power of this technique in efficient positioning of coding regions on the physical maps.


Subject(s)
Chromosomes, Human, Pair 13 , In Situ Hybridization, Fluorescence , Pseudogenes , RNA Nucleotidyltransferases/genetics , Transcription Factors/genetics , Humans , In Situ Hybridization, Fluorescence/methods , Nuclear Proteins , RNA Helicases
7.
Ann Med ; 29(4): 291-6, 1997 Aug.
Article in English | MEDLINE | ID: mdl-9375985

ABSTRACT

We wanted to investigate whether rheumatoid arthritis (RA) patients, defined by the American College of Rheumatology (ACR) 1987 criteria and selected from one community by the help of the official Finnish data registers, share the common HLA susceptibility genes. The HLA frequencies of 88 RA patients representing 85% of the prevalent cases of RA in the community were compared with those of 188 healthy controls. Fifty-four per cent of the index cases with RA had DR4 compared with 30% of the healthy controls (P <0.001). The 'RA susceptibility sequence' was found in 75% of the DRB1 genes in the index cases, but it did not correlate with the severity of the disease. The frequency of DR3 was not increased in RA patients but it was associated with features of severe disease, that is, with a high erythrocyte sedimentation rate (P<0.05), extra-articular disease (P<0.01) and prostheses in large joints (P<0.05). According to our results community-based RA patients satisfying the new ACR criteria show the common DR4 association. DR3 was the only HLA allele which showed some disease-modifying effect correlating with the severity of RA.


Subject(s)
Arthritis, Rheumatoid/immunology , HLA Antigens/genetics , Adult , Aged , Alleles , Arthritis, Rheumatoid/genetics , Arthritis, Rheumatoid/physiopathology , Female , HLA Antigens/metabolism , HLA-DR3 Antigen/genetics , HLA-DR3 Antigen/metabolism , Humans , Joint Prosthesis , Male , Middle Aged
8.
Genomics ; 39(2): 185-91, 1997 Jan 15.
Article in English | MEDLINE | ID: mdl-9027505

ABSTRACT

Infantile onset spinocerebellar ataxia (IOSCA) is a progressive neurological disorder of unknown etiology. It is inherited as an autosomal recessive trait and has so far been reported in just 19 Finnish patients in 13 separate families. We have previously assigned the IOSCA locus (HGMW-approved symbol SCA8) to chromosome 10q, where no previously identified ataxia loci are located. Haplotype analysis combined with genealogical data provided evidence that all the IOSCA cases in Finland originate from a single 30- to 40-generation-old founder mutation. By analyzing extended disease haplotypes observed today, the IOSCA locus can now be restricted to a region between two adjacent microsatellites, D10S192 and D10S1265, with no genetic intermarker distance. We have constructed a detailed physical map of this 270-kb IOSCA region and cytogenetically localized it to 10q24. We have also assigned two previously known genes, PAX2 and CYP17, more precisely into this region, but the sequence analysis of coding regions of these two genes has not revealed mutations in an IOSCA patient. The obtained long-range clones will form the basis for the isolation of a novel ataxia gene.


Subject(s)
Chromosome Mapping , Chromosomes, Human, Pair 10 , Spinocerebellar Degenerations/genetics , Cloning, Molecular , Haplotypes , Humans , Hybrid Cells/radiation effects , In Situ Hybridization, Fluorescence , Linkage Disequilibrium , Molecular Sequence Data , Sequence Tagged Sites
9.
Genome Res ; 6(10): 1002-12, 1996 Oct.
Article in English | MEDLINE | ID: mdl-8908520

ABSTRACT

In positional cloning the initial assignment of a gene to a specific chromosomal locus is followed by physical mapping of the critical region. The construction of a high-resolution physical map still involves considerable effort. However, new high-resolution fluorescence in situ hybridization (FISH) techniques have facilitated this process substantially. Here we summarize a strategy that combines a spectrum of FISH techniques [metaphase, interphase, mechanically stretched chromosomes (MSCs), and fiber-FISH on free chromatin] for the construction and characterization of a high-resolution physical map for a positional cloning project. The chromosomal region 13q22, containing the locus of the variant form of the neuronal ceroid lipofuscinosis (vLINCL, CLN5) disease, serves here as an example for this process. We used metaphase FISH to exclude positionally a candidate gene, to refine the locus to 13q22, and to analyze the possible chimerism of the YACs in the region. Both metaphase and interphase FISH techniques were applied to determine the low-resolution distances between the restricting markers. FISH using MSCs confirmed the centromeric-telomeric order of the clones and facilitated the estimation of the size of the gaps between the clones. Finally, fiber-FISH was found to be the method of choice for the construction of an accurate high-resolution map of the contig established over the restricted region. Thus, FISH techniques in combination with genetic mapping data enabled the refinement of the initial 4-cM region to a high-resolution map of only 400 kb in length. Here the FISH strategy replaced the need for many laborious traditional physical mapping methods, e.g., pulsed-field gel electrophoresis.


Subject(s)
Chromosomes, Human, Pair 13 , Cloning, Molecular , In Situ Hybridization, Fluorescence , Aminopeptidases , Chromosome Mapping , Chromosomes, Artificial, Yeast , Cosmids , Dipeptidyl-Peptidases and Tripeptidyl-Peptidases , Genetic Linkage , Genetic Markers , Humans , Neuronal Ceroid-Lipofuscinoses/genetics , Polymorphism, Genetic , Serine Endopeptidases/genetics
10.
Genomics ; 37(1): 62-7, 1996 Oct 01.
Article in English | MEDLINE | ID: mdl-8921371

ABSTRACT

Two phenotypic presentations of excessive accumulation of free sialic acid in lysosomes, Salla disease and infantile sialic acid storage disease, have been assigned to the same locus at 6q14-q15. Here we have restricted the critical DNA region by analyses of extended haplotypes and constructed a long-range physical contig over the critical 200-kb chromosomal region flanked by the markers D6S280 and D6S1622. The efficient fiber-FISH technique was applied to order and orient the clones, and this facilitated avoidance of the tedious restriction mapping by pulsed-field gel electrophoresis. We excluded all seven known ESTs and nine cDNAs assigned to this DNA region and tentatively identified two potential CpG islands within the region, which now represent positional candidate genes for the sialic acid storage disorders.


Subject(s)
Chromosomes, Human, Pair 6 , Lysosomes/metabolism , Membrane Transport Proteins/genetics , Organic Anion Transporters , Symporters , Cloning, Molecular , DNA, Complementary , Dinucleoside Phosphates/genetics , Female , Finland , Humans , In Situ Hybridization, Fluorescence , Intracellular Membranes/metabolism , Male , Metabolism, Inborn Errors/genetics , Pedigree , Recombination, Genetic
11.
Genomics ; 35(1): 71-8, 1996 Jul 01.
Article in English | MEDLINE | ID: mdl-8661106

ABSTRACT

The variant form of late infantile neuronal ceroid lipofuscinosis (vLINCL, locus definition CLN5) represents a progressive brain disease with autosomal recessive inheritance. We have previously assigned the CLN5 locus to chromosome 13q21.1-q32 between markers D13S160 and D13S162 by linkage analysis in Finnish families. The information on ancient recombination events obtained from linkage disequilibrium provided an efficient tool for further refining the assignment of the CLN5 locus. Isolation of two novel (CA)n markers, COLAC1 and AC224, resulted in a dramatic restriction of the critical DNA region. We utilized the Fiber-FISH technique to orient and order the large DNA clones isolated by STSs and were able to eliminate almost totally the restriction digestion and PFGE step in the construction of the long-range DNA contig. Both linkage disequilibrium data and Fiber-FISH analyses assigned the CLN5 locus to a well-defined 200-kb region. Here we report a complete physical map of about 350 kb covering the critical chromosomal region of CLN5, which will facilitate the final isolation of the CLN5 gene.


Subject(s)
Chromosome Mapping/methods , Chromosomes, Human, Pair 13/genetics , In Situ Hybridization, Fluorescence/methods , Neuronal Ceroid-Lipofuscinoses/genetics , Base Sequence , Child, Preschool , Chromosome Walking , Chromosomes, Artificial, Yeast/genetics , Chromosomes, Human, Pair 13/ultrastructure , Female , Genetic Markers , Haplotypes , Humans , Image Processing, Computer-Assisted , Linkage Disequilibrium , Male , Molecular Sequence Data , Neuronal Ceroid-Lipofuscinoses/classification , Pedigree , Polymerase Chain Reaction , Recombination, Genetic
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