Literature DB >> 15781871

Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6.

Thaddeus P Dryja1, Terri L McGee, Eliot L Berson, Gerald A Fishman, Michael A Sandberg, Kenneth R Alexander, Deborah J Derlacki, Aruna S Rajagopalan.   

Abstract

We report three unrelated patients with mutations in the GRM6 gene that normally encodes the glutamate receptor mGluR6. This neurotransmitter receptor has been shown previously to be present only in the synapses of the ON bipolar cell dendrites, and it mediates synaptic transmission from rod and cone photoreceptors to this type of second-order neuron. Despite the synaptic defect, best visual acuities were normal or only moderately reduced (20/15 to 20/40). The patients were night blind from an early age, and when maximally dark-adapted, they could perceive lights only with an intensity equal to or slightly dimmer than that normally detected by the cone system (i.e., 2-3 log units above normal). Electroretinograms (ERGs) in response to single brief flashes of light had clearly detectable a-waves, which are derived from photoreceptors, and greatly reduced b-waves, which are derived from the second-order inner retinal neurons. ERGs in response to sawtooth flickering light indicated a markedly reduced ON response and a nearly normal OFF response. There was no subjective delay in the perception of suddenly appearing white vs. black objects on a gray background. These patients exemplify a previously unrecognized, autosomal recessive form of congenital night blindness associated with a negative ERG waveform.

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Year:  2005        PMID: 15781871      PMCID: PMC555731          DOI: 10.1073/pnas.0501233102

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  57 in total

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2.  On-off interaction in the human electroretinogram.

Authors:  C I HOWARTH
Journal:  J Opt Soc Am       Date:  1961-03

3.  Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseases.

Authors:  Dror Sharon; Hiroyuki Yamamoto; Terri L McGee; Vivian Rabe; Robert T Szerencsei; Robert J Winkfein; Clemens F M Prinsen; Claire S Barnes; Sten Andreasson; Gerald A Fishman; Paul P M Schnetkamp; Eliot L Berson; Thaddeus P Dryja
Journal:  Invest Ophthalmol Vis Sci       Date:  2002-06       Impact factor: 4.799

4.  Normal values for the Pelli-Robson contrast sensitivity test.

Authors:  M Mäntyjärvi; T Laitinen
Journal:  J Cataract Refract Surg       Date:  2001-02       Impact factor: 3.351

5.  Structural basis of glutamate recognition by a dimeric metabotropic glutamate receptor.

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Journal:  Nature       Date:  2000-10-26       Impact factor: 49.962

6.  The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.

Authors:  C M Pusch; C Zeitz; O Brandau; K Pesch; H Achatz; S Feil; C Scharfe; J Maurer; F K Jacobi; A Pinckers; S Andreasson; A Hardcastle; B Wissinger; W Berger; A Meindl
Journal:  Nat Genet       Date:  2000-11       Impact factor: 38.330

7.  Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.

Authors:  N T Bech-Hansen; M J Naylor; T A Maybaum; R L Sparkes; B Koop; D G Birch; A A Bergen; C F Prinsen; R C Polomeno; A Gal; A V Drack; M A Musarella; S G Jacobson; R S Young; R G Weleber
Journal:  Nat Genet       Date:  2000-11       Impact factor: 38.330

8.  Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene.

Authors:  H P Scholl; H Langrová; C M Pusch; B Wissinger; E Zrenner; E Apfelstedt-Sylla
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9.  A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction.

Authors:  Claire S Barnes; Kenneth R Alexander; Gerald A Fishman
Journal:  Ophthalmology       Date:  2002-03       Impact factor: 12.079

Review 10.  [Establishment of the concept of new clinical entities--complete and incomplete form of congenital stationary night blindness].

Authors:  Yozo Miyake
Journal:  Nippon Ganka Gakkai Zasshi       Date:  2002-12
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  113 in total

1.  On- and off-response ERGs elicited by sawtooth stimuli in normal subjects and glaucoma patients.

Authors:  Gobinda Pangeni; Robert Lämmer; Ralf P Tornow; Folkert K Horn; Jan Kremers
Journal:  Doc Ophthalmol       Date:  2012-03-29       Impact factor: 2.379

2.  An extended 15 Hz ERG protocol (2): data of normal subjects and patients with achromatopsia, CSNB1, and CSNB2.

Authors:  Mieke M C Bijveld; Frans C C Riemslag; Astrid M L Kappers; Frank P Hoeben; Maria M van Genderen
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3.  Asymmetrical growth of the photopic hill during the light adaptation effect.

Authors:  Marie-Lou Garon; Marianne Rufiange; Ruth Hamilton; Daphne L McCulloch; Pierre Lachapelle
Journal:  Doc Ophthalmol       Date:  2010-08-15       Impact factor: 2.379

Review 4.  Retinal remodeling.

Authors:  B W Jones; M Kondo; H Terasaki; Y Lin; M McCall; R E Marc
Journal:  Jpn J Ophthalmol       Date:  2012-05-30       Impact factor: 2.447

5.  Sensitivity and kinetics of signal transmission at the first visual synapse differentially impact visually-guided behavior.

Authors:  Ignacio Sarria; Johan Pahlberg; Yan Cao; Alexander V Kolesnikov; Vladimir J Kefalov; Alapakkam P Sampath; Kirill A Martemyanov
Journal:  Elife       Date:  2015-04-16       Impact factor: 8.140

6.  Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness.

Authors:  Miranda L Scalabrino; Sanford L Boye; Kathryn M H Fransen; Jennifer M Noel; Frank M Dyka; Seok Hong Min; Qing Ruan; Charles N De Leeuw; Elizabeth M Simpson; Ronald G Gregg; Maureen A McCall; Neal S Peachey; Shannon E Boye
Journal:  Hum Mol Genet       Date:  2015-08-26       Impact factor: 6.150

7.  Congenital stationary night blindness associated with mutations in GRM6 encoding glutamate receptor MGluR6.

Authors:  E O'Connor; L E Allen; K Bradshaw; J Boylan; A T Moore; D Trump
Journal:  Br J Ophthalmol       Date:  2006-05       Impact factor: 4.638

8.  Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus).

Authors:  Rebecca R Bellone; Samantha A Brooks; Lynne Sandmeyer; Barbara A Murphy; George Forsyth; Sheila Archer; Ernest Bailey; Bruce Grahn
Journal:  Genetics       Date:  2008-07-27       Impact factor: 4.562

9.  TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade.

Authors:  Chieko Koike; Takehisa Obara; Yoshitsugu Uriu; Tomohiro Numata; Rikako Sanuki; Kentarou Miyata; Toshiyuki Koyasu; Shinji Ueno; Kazuo Funabiki; Akiko Tani; Hiroshi Ueda; Mineo Kondo; Yasuo Mori; Masao Tachibana; Takahisa Furukawa
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-04       Impact factor: 11.205

10.  Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.

Authors:  Christina Zeitz; Samuel G Jacobson; Christian P Hamel; Kinga Bujakowska; Marion Neuillé; Elise Orhan; Xavier Zanlonghi; Marie-Elise Lancelot; Christelle Michiels; Sharon B Schwartz; Béatrice Bocquet; Aline Antonio; Claire Audier; Mélanie Letexier; Jean-Paul Saraiva; Tien D Luu; Florian Sennlaub; Hoan Nguyen; Olivier Poch; Hélène Dollfus; Odile Lecompte; Susanne Kohl; José-Alain Sahel; Shomi S Bhattacharya; Isabelle Audo
Journal:  Am J Hum Genet       Date:  2012-12-13       Impact factor: 11.025

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