Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds).

PubWeight™: 3.31‹?› | Rank: Top 1%

🔗 View Article (PMID 2918924)

Published in Nature on March 02, 1989

Authors

G H Travis1, M B Brennan, P E Danielson, C A Kozak, J G Sutcliffe

Author Affiliations

1: Research Institute of Scripps Clinic, Department of Molecular Biology, La Jolla, California 92037.

Articles citing this

In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse. Hum Mol Genet (2006) 3.90

Apoptotic photoreceptor cell death in mouse models of retinitis pigmentosa. Proc Natl Acad Sci U S A (1994) 2.58

Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments. Proc Natl Acad Sci U S A (1996) 2.36

Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice. J Clin Invest (2008) 2.24

Localization of peripherin/rds in the disk membranes of cone and rod photoreceptors: relationship to disk membrane morphogenesis and retinal degeneration. J Cell Biol (1992) 2.17

Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse. Proc Natl Acad Sci U S A (1991) 2.11

A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse. Proc Natl Acad Sci U S A (2000) 1.88

Kidney failure in mice lacking the tetraspanin CD151. J Cell Biol (2006) 1.85

Retention of function without normal disc morphogenesis occurs in cone but not rod photoreceptors. J Cell Biol (2006) 1.70

Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration. Am J Hum Genet (2006) 1.63

Characterization of mice lacking the tetraspanin superfamily member CD151. Mol Cell Biol (2004) 1.57

Defective subunit assembly underlies a digenic form of retinitis pigmentosa linked to mutations in peripherin/rds and rom-1. Proc Natl Acad Sci U S A (1996) 1.43

Drosophila retinal degeneration A gene encodes an eye-specific diacylglycerol kinase with cysteine-rich zinc-finger motifs and ankyrin repeats. Proc Natl Acad Sci U S A (1993) 1.38

The L6 membrane proteins--a new four-transmembrane superfamily. Protein Sci (2000) 1.24

The 27-kD diphtheria toxin receptor-associated protein (DRAP27) from vero cells is the monkey homologue of human CD9 antigen: expression of DRAP27 elevates the number of diphtheria toxin receptors on toxin-sensitive cells. J Cell Biol (1992) 1.24

Photoreceptor renewal: a role for peripherin/rds. Int Rev Cytol (2002) 1.23

Electrophysiological analysis of visual function in mutant mice. Doc Ophthalmol (2003) 1.22

Deficiency of rds/peripherin causes photoreceptor death in mouse models of digenic and dominant retinitis pigmentosa. Proc Natl Acad Sci U S A (2001) 1.19

The role of subunit assembly in peripherin-2 targeting to rod photoreceptor disk membranes and retinitis pigmentosa. Mol Biol Cell (2003) 1.19

Membrane frizzled-related protein is necessary for the normal development and maintenance of photoreceptor outer segments. Vis Neurosci (2008) 1.18

Naturally occurring animal models with outer retina phenotypes. Vision Res (2009) 1.14

Protein sorting, targeting and trafficking in photoreceptor cells. Prog Retin Eye Res (2013) 1.13

P2Y(2) receptor agonist INS37217 enhances functional recovery after detachment caused by subretinal injection in normal and rds mice. Invest Ophthalmol Vis Sci (2003) 1.10

Proteasome overload is a common stress factor in multiple forms of inherited retinal degeneration. Proc Natl Acad Sci U S A (2013) 1.10

RDS/peripherin gene mutations are frequent causes of central retinal dystrophies. J Med Genet (1997) 1.09

Role of the second intradiscal loop of peripherin/rds in homo and hetero associations. Biochemistry (2005) 1.05

Neuroprotection of photoreceptors by direct delivery of erythropoietin to the retina of the retinal degeneration slow mouse. Exp Eye Res (2009) 1.04

Cloning of a growth arrest-specific and transforming growth factor beta-regulated gene, TI 1, from an epithelial cell line. Mol Cell Biol (1991) 1.01

Uncoupling of photoreceptor peripherin/rds fusogenic activity from biosynthesis, subunit assembly, and targeting: a potential mechanism for pathogenic effects. J Biol Chem (2004) 0.99

Folding and subunit assembly of photoreceptor peripherin/rds is mediated by determinants within the extracellular/intradiskal EC2 domain: implications for heterogeneous molecular pathologies. J Biol Chem (2001) 0.98

A peptide analogue to a fusion domain within photoreceptor peripherin/rds promotes membrane adhesion and depolarization. Biochim Biophys Acta (2000) 0.97

Molecular characterization of the skate peripherin/rds gene: relationship to its orthologues and paralogues. Invest Ophthalmol Vis Sci (2003) 0.97

Extensive intrafamilial and interfamilial phenotypic variation among patients with autosomal dominant retinal dystrophy and mutations in the human RDS/peripherin gene. Br J Ophthalmol (1995) 0.95

Identification of photoreceptor genes affected by PRPF31 mutations associated with autosomal dominant retinitis pigmentosa. Neurobiol Dis (2007) 0.95

Nucleotide and predicted protein sequence of rat retinal degeneration slow (rds). Nucleic Acids Res (1990) 0.94

An unconventional secretory pathway mediates the cilia targeting of peripherin/rds. J Neurosci (2014) 0.94

Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM. Am J Hum Genet (1992) 0.93

Deletional analysis of the rod photoreceptor cell peripherin/RDS carboxy-terminal region. Exp Eye Res (2002) 0.93

A single valine residue plays an essential role in peripherin/rds targeting to photoreceptor outer segments. PLoS One (2013) 0.92

Light-evoked responses of the retinal pigment epithelium: changes accompanying photoreceptor loss in the mouse. J Neurophysiol (2010) 0.92

Genetic supplementation of RDS alleviates a loss-of-function phenotype in C214S model of retinitis pigmentosa. Adv Exp Med Biol (2008) 0.90

PCR driven DNA-DNA competitive hybridization: a new method for sensitive differential cloning. Nucleic Acids Res (1991) 0.89

Molecular ophthalmology: an update on animal models for retinal degenerations and dystrophies. Br J Ophthalmol (2000) 0.89

Identification of candidate genes for human retinal degeneration loci using differentially expressed genes from mouse photoreceptor dystrophy models. Mol Vis (2008) 0.87

A novel mutation in Prph2, a gene regulated by Nr2e3, causes retinal degeneration and outer-segment defects similar to Nr2e3 ( rd7/rd7 ) retinas. Mamm Genome (2008) 0.87

Photoreceptors at a glance. J Cell Sci (2015) 0.87

Topological analysis of peripherin/rds and abnormal glycosylation of the pathogenic Pro216-->Leu mutation. Biochem J (2002) 0.85

Transgenic expression of constitutively active RAC1 disrupts mouse rod morphogenesis. Invest Ophthalmol Vis Sci (2014) 0.85

Heterologous expression of WT and mutant photoreceptor peripherin/rds in Madin Darby canine kidney cells: an assessment of fusogenic function. Exp Eye Res (2002) 0.85

AAV-mediated gene therapy in mouse models of recessive retinal degeneration. Curr Mol Med (2012) 0.84

A monogenic dominant mutation in Rom1 generated by N-ethyl-N-nitrosourea mutagenesis causes retinal degeneration in mice. Mol Vis (2010) 0.83

Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin. Am J Hum Genet (1992) 0.82

ROM-1 potentiates photoreceptor specific membrane fusion processes. Exp Eye Res (2006) 0.82

Protective gene expression changes elicited by an inherited defect in photoreceptor structure. PLoS One (2012) 0.82

Cell loss in retinal dystrophies by apoptosis--death by informed consent! Br J Ophthalmol (1995) 0.82

Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa. Am J Hum Genet (1996) 0.82

Photoreceptor discs form through peripherin-dependent suppression of ciliary ectosome release. J Cell Biol (2017) 0.81

Deciphering the structure and function of Als2cr4 in the mouse retina. Invest Ophthalmol Vis Sci (2010) 0.81

The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosa. Am J Hum Genet (1992) 0.80

Molecular genetics of retinitis pigmentosa. West J Med (1991) 0.79

Light regulates the ciliary protein transport and outer segment disc renewal of mammalian photoreceptors. Dev Cell (2015) 0.79

Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 (PRPH2) Causing Autosomal Dominant Retinal Dystrophies. JAMA Ophthalmol (2015) 0.78

Molecular advances in retinitis pigmentosa. West J Med (1991) 0.77

Multimodal imaging of adult-onset foveomacular vitelliform dystrophy. Saudi J Ophthalmol (2014) 0.77

PRPH2/RDS and ROM-1: Historical context, current views and future considerations. Prog Retin Eye Res (2016) 0.77

Three polymorphisms detected by a retinal degeneration slow (rds) probe (RDS). Nucleic Acids Res (1991) 0.77

Structural and molecular bases of rod photoreceptor morphogenesis and disease. Prog Retin Eye Res (2016) 0.76

Molecular genetics of macular dystrophies. Br J Ophthalmol (1996) 0.75

Sequenase should be used instead of the Klenow fragment for the synthesis of oligonucleotides labeled to a high specific activity. Nucleic Acids Res (1991) 0.75

Gene therapy for PRPH2-associated ocular disease: challenges and prospects. Cold Spring Harb Perspect Med (2014) 0.75

Insights from Genetic Model Systems of Retinal Degeneration: Role of Epsins in Retinal Angiogenesis and VEGFR2 Signaling. J Nat Sci (2017) 0.75

New nucleotide sequence data on the EMBL File Server. Nucleic Acids Res (1990) 0.75

Longitudinal assessment of retinal structure and function reveals a rod-cone degeneration in a guinea pig model initially presented as night blind. Doc Ophthalmol (2011) 0.75

Articles by these authors

Complete nucleotide sequence of the Escherichia coli plasmid pBR322. Cold Spring Harb Symp Quant Biol (1979) 43.48

Nucleotide sequence of Moloney murine leukaemia virus. Nature (1981) 24.82

Nucleotide sequence of the ampicillin resistance gene of Escherichia coli plasmid pBR322. Proc Natl Acad Sci U S A (1978) 19.34

pBR322 restriction map derived from the DNA sequence: accurate DNA size markers up to 4361 nucleotide pairs long. Nucleic Acids Res (1978) 13.22

Neurons containing hypocretin (orexin) project to multiple neuronal systems. J Neurosci (1998) 9.88

The hypocretins: hypothalamus-specific peptides with neuroexcitatory activity. Proc Natl Acad Sci U S A (1998) 9.32

Immunogenic structure of the influenza virus hemagglutinin. Cell (1982) 8.93

Protection against foot-and-mouth disease by immunization with a chemically synthesized peptide predicted from the viral nucleotide sequence. Nature (1982) 5.50

p1B15: a cDNA clone of the rat mRNA encoding cyclophilin. DNA (1988) 4.89

Obesity in the mouse model of pro-opiomelanocortin deficiency responds to peripheral melanocortin. Nat Med (1999) 4.78

Chemical synthesis of a polypeptide predicted from nucleotide sequence allows detection of a new retroviral gene product. Nature (1980) 4.35

Chemically synthesized peptides predicted from the nucleotide sequence of the hepatitis B virus genome elicit antibodies reactive with the native envelope protein of Dane particles. Proc Natl Acad Sci U S A (1981) 4.26

A restriction enzyme Tha I from the thermophilic mycoplasma Thermoplasma acidophilum. Nucleic Acids Res (1978) 4.25

Association of human herpes virus 6 (HHV-6) with multiple sclerosis: increased IgM response to HHV-6 early antigen and detection of serum HHV-6 DNA. Nat Med (1997) 3.65

Tie-1 and tie-2 define another class of putative receptor tyrosine kinase genes expressed in early embryonic vascular system. Proc Natl Acad Sci U S A (1993) 3.37

Influenza virus-susceptible mice carry Mx genes with a large deletion or a nonsense mutation. Mol Cell Biol (1988) 3.32

Sequence-specific antibodies show that maturation of Moloney leukemia virus envelope polyprotein involves removal of a COOH-terminal peptide. Proc Natl Acad Sci U S A (1981) 3.13

Prospective observational study of sentinel lymphadenectomy without further axillary dissection in patients with sentinel node-negative breast cancer. J Clin Oncol (2000) 3.13

Nucleotide sequence of Moloney leukemia virus: 3' end reveals details of replications, analogy to bacterial transposons, and an unexpected gene. Proc Natl Acad Sci U S A (1980) 2.90

A sequential staining technique for the chromosomal analysis of the interspecific mouse/hamster and mouse/human somatic cell hybrids. Exp Cell Res (1977) 2.71

The cleavage site of the restriction endonuclease Ava II. Nucleic Acids Res (1978) 2.60

Genetic mapping of the ecotropic murine leukemia virus-inducing locus of BALB/c mouse to chromosome 5. Science (1979) 2.54

The alpha-spectrin gene is on chromosome 1 in mouse and man. Proc Natl Acad Sci U S A (1985) 2.53

Germ-line reinsertions of AKR murine leukemia virus genomes in Akv-1 congenic mice. Proc Natl Acad Sci U S A (1980) 2.52

Gene expression in rat brain. Nucleic Acids Res (1983) 2.40

The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNA. Genomics (1991) 2.39

Identification of CRAMP, a cathelin-related antimicrobial peptide expressed in the embryonic and adult mouse. J Biol Chem (1997) 2.38

Genetic mapping of xenotropic murine leukemia virus-inducing loci in five mouse strains. J Exp Med (1980) 2.34

rax, a novel paired-type homeobox gene, shows expression in the anterior neural fold and developing retina. Proc Natl Acad Sci U S A (1997) 2.29

Genetic mapping of the ecotropic virus-inducing locus Akv-2 of the AKR mouse. J Exp Med (1980) 2.29

Mature microglia resemble immature antigen-presenting cells. Glia (1998) 2.28

Transgenic mice expressing beta-galactosidase in mature neurons under neuron-specific enolase promoter control. Neuron (1990) 2.26

Chromosome mapping and expression of a putative testis-determining gene in mouse. Science (1989) 2.22

Frequent provirus insertional mutagenesis of Notch1 in thymomas of MMTVD/myc transgenic mice suggests a collaboration of c-myc and Notch1 for oncogenesis. Genes Dev (1996) 2.18

Targeted deletion of the Vgf gene indicates that the encoded secretory peptide precursor plays a novel role in the regulation of energy balance. Neuron (1999) 2.15

Nucleotide sequences of two mRNAs for rat brain myelin proteolipid protein. Cell (1985) 2.10

The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein. Neuron (1991) 2.07

The genomic structure of the murine ICSBP gene reveals the presence of the gamma interferon-responsive element, to which an ISGF3 alpha subunit (or similar) molecule binds. Mol Cell Biol (1993) 2.06

Hypocretin-1 modulates rapid eye movement sleep through activation of locus coeruleus neurons. J Neurosci (2000) 2.05

Transcriptional activation of the mouse Mx gene by type I interferon. Mol Cell Biol (1986) 2.04

Cartilage-derived morphogenetic proteins. New members of the transforming growth factor-beta superfamily predominantly expressed in long bones during human embryonic development. J Biol Chem (1994) 2.03

Structural and functional studies of the early T lymphocyte activation 1 (Eta-1) gene. Definition of a novel T cell-dependent response associated with genetic resistance to bacterial infection. J Exp Med (1989) 2.02

Identifying the protein products of brain-specific genes with antibodies to chemically synthesized peptides. Cell (1983) 2.01

Chemically synthesized peptides of hepatitis B surface antigen duplicate the d/y specificities and induce subtype-specific antibodies in chimpanzees. Proc Natl Acad Sci U S A (1983) 2.00

Full-length sequence, localization, and chromosomal mapping of ameloblastin. A novel tooth-specific gene. J Biol Chem (1996) 2.00

Common 82-nucleotide sequence unique to brain RNA. Proc Natl Acad Sci U S A (1982) 1.98

The mouse homolog of the Gibbon ape leukemia virus receptor: genetic mapping and a possible receptor function in rodents. Virology (1991) 1.97

A melanocyte-specific gene, Pmel 17, maps near the silver coat color locus on mouse chromosome 10 and is in a syntenic region on human chromosome 12. Proc Natl Acad Sci U S A (1991) 1.97

Identifier sequences are transcribed specifically in brain. Nature (1984) 1.95

Susceptibility of wild mouse cells to exogenous infection with xenotropic leukemia viruses: control by a single dominant locus on chromosome 1. J Virol (1985) 1.95

Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan gene. Nat Genet (1994) 1.94

A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse. Proc Natl Acad Sci U S A (2000) 1.88

Hypocretin/orexin- and melanin-concentrating hormone-expressing cells form distinct populations in the rodent lateral hypothalamus: relationship to the neuropeptide Y and agouti gene-related protein systems. J Comp Neurol (1998) 1.87

Antibodies that react with predetermined sites on proteins. Science (1983) 1.87

Murine endogenous retroviruses. Cell Mol Life Sci (2008) 1.85

Mapping of murine interferon-alpha genes to chromosome 4. Gene (1983) 1.79

Genetic mapping of a mouse chromosomal locus required for mink cell focus-forming virus replication. J Virol (1983) 1.79

Do all patients with sentinel node metastasis from breast carcinoma need complete axillary node dissection? Ann Surg (1999) 1.77

Diverse wild mouse origins of xenotropic, mink cell focus-forming, and two types of ecotropic proviral genes. J Virol (1987) 1.77

Functional expression of the murine connexin 36 gene coding for a neuron-specific gap junctional protein. J Membr Biol (2000) 1.74

Genomic organization, chromosomal mapping, and promoter analysis of the mouse dentin sialophosphoprotein (Dspp) gene, which codes for both dentin sialoprotein and dentin phosphoprotein. J Biol Chem (1998) 1.73

Brain-specific genes have identifier sequences in their introns. Proc Natl Acad Sci U S A (1984) 1.71

Pronociceptive actions of dynorphin maintain chronic neuropathic pain. J Neurosci (2001) 1.67

The chromosomal distribution of mouse odorant receptor genes. Proc Natl Acad Sci U S A (1996) 1.66

Identification of a second interferon-regulated murine Mx gene. Mol Cell Biol (1988) 1.62

Expression of Brca1 is associated with terminal differentiation of ectodermally and mesodermally derived tissues in mice. Genes Dev (1995) 1.61

Chromosomal locations of the gene coding for the CD3 (T3) gamma subunit of the human and mouse CD3/T-cell antigen receptor complexes. Immunogenetics (1987) 1.60

The Sfpi-1 proviral integration site of Friend erythroleukemia encodes the ets-related transcription factor Pu.1. J Virol (1991) 1.58

An endoplasmic reticulum-specific cyclophilin. Mol Cell Biol (1991) 1.57

Two forms of 1B236/myelin-associated glycoprotein, a cell adhesion molecule for postnatal neural development, are produced by alternative splicing. Proc Natl Acad Sci U S A (1987) 1.57

Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus. J Biol Chem (1994) 1.56

Phenol emulsion-enhanced DNA-driven subtractive cDNA cloning: isolation of low-abundance monkey cortex-specific mRNAs. Proc Natl Acad Sci U S A (1988) 1.56

Nonecotropic murine leukemia viruses in BALB/c and NFS/N mice: characterization of the BALB/c Bxv-1 provirus and the single NFS endogenous xenotrope. J Virol (1986) 1.53

Antibodies to chemically synthesized peptides predicted from DNA sequences as probes of gene expression. Cell (1981) 1.52

A unique sequence related to the ecotropic murine leukemia virus is associated with the Fv-4 resistance gene. Proc Natl Acad Sci U S A (1984) 1.51

Control of neuronal gene expression. Science (1984) 1.50

Rhes: A striatal-specific Ras homolog related to Dexras1. J Neurosci Res (1999) 1.49

Genetic mapping of the mouse c-fms proto-oncogene to chromosome 18. J Virol (1988) 1.48

Regional linkage analysis of the dioxin-inducible P-450 gene family on mouse chromosome 9. Biochem Biophys Res Commun (1985) 1.47

The Lake Casitas wild mouse: evolving genetic resistance to retroviral disease. Trends Genet (1991) 1.46

cDNA cloning and characterization of three genes uniquely expressed in cerebellum by Purkinje neurons. J Neurosci (1988) 1.43

Does sentinel lymphadenectomy improve staging and alter therapy in elderly women with breast cancer? Ann Surg Oncol (2000) 1.41

Mouse lymphotoxin-beta receptor. Molecular genetics, ligand binding, and expression. J Immunol (1995) 1.41

Genetic mapping of the gene for Ca2+/calmodulin-dependent protein kinase IV (Camk-4) to mouse chromosome 18. Genomics (1990) 1.40

Genetic mapping of ecotropic murine leukemia virus-inducing loci in six inbred strains. J Exp Med (1982) 1.40

Synthetic peptide immunogens as vaccines. Annu Rev Microbiol (1983) 1.39

Cellular localization and function of the proteins encoded by brain-specific mRNAs. Cold Spring Harb Symp Quant Biol (1983) 1.36

Overview of the most prevalent hypothalamus-specific mRNAs, as identified by directional tag PCR subtraction. Proc Natl Acad Sci U S A (1996) 1.36

Differential expansion of the N-formylpeptide receptor gene cluster in human and mouse. Genomics (1998) 1.36

Fatty acid amide hydrolase, the degradative enzyme for anandamide and oleamide, has selective distribution in neurons within the rat central nervous system. J Neurosci Res (1997) 1.35

EHD1--an EH-domain-containing protein with a specific expression pattern. Genomics (1999) 1.35

Activation of erythropoietin receptors by Friend viral gp55 and by erythropoietin and down-modulation by the murine Fv-2r resistance gene. Proc Natl Acad Sci U S A (1990) 1.33

Increased HTLV-I proviral load and preferential expansion of HTLV-I Tax-specific CD8+ T cells in cerebrospinal fluid from patients with HAM/TSP. Ann Neurol (2001) 1.33

A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locus. Hum Mol Genet (1999) 1.33