Literature DB >> 10414956

Myosin VIIa participates in opsin transport through the photoreceptor cilium.

X Liu1, I P Udovichenko, S D Brown, K P Steel, D S Williams.   

Abstract

Two types of Usher syndrome, a blindness-deafness disorder, result from mutations in the myosin VIIa gene. As for most other unconventional myosins, little is known about the function or functions of myosin VIIa. Here, we studied the photoreceptor cells of mice with mutant myosin VIIa by electron immunomicroscopy and microscopic autoradiography. We found evidence that myosin VIIa functions in the connecting cilium of each photoreceptor cell and participates in the transport of opsin through this structure. These findings provide the first direct evidence that opsin travels along the connecting cilium en route to the outer segment. They demonstrate that a myosin may function in a cilium and suggest that abnormal opsin transport might contribute to blindness in Usher syndrome.

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Year:  1999        PMID: 10414956      PMCID: PMC6782817     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  53 in total

1.  Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.

Authors:  M D Weston; P M Kelley; L D Overbeck; M Wagenaar; D J Orten; T Hasson; Z Y Chen; D Corey; M Mooseker; J Sumegi; C Cremers; C Moller; S G Jacobson; M B Gorin; W J Kimberling
Journal:  Am J Hum Genet       Date:  1996-11       Impact factor: 11.025

2.  Purification and light-dependent phosphorylation of a candidate fusion protein, the photoreceptor cell peripherin/rds.

Authors:  K Boesze-Battaglia; F Kong; O P Lamba; F P Stefano; D S Williams
Journal:  Biochemistry       Date:  1997-06-03       Impact factor: 3.162

3.  Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B.

Authors:  Z Y Chen; T Hasson; P M Kelley; B J Schwender; M F Schwartz; M Ramakrishnan; W J Kimberling; M S Mooseker; D P Corey
Journal:  Genomics       Date:  1996-09-15       Impact factor: 5.736

4.  Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.

Authors:  A Adato; D Weil; H Kalinski; Y Pel-Or; H Ayadi; C Petit; M Korostishevsky; B Bonne-Tamir
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

5.  Defective myosin VIIA gene responsible for Usher syndrome type 1B.

Authors:  D Weil; S Blanchard; J Kaplan; P Guilford; F Gibson; J Walsh; P Mburu; A Varela; J Levilliers; M D Weston
Journal:  Nature       Date:  1995-03-02       Impact factor: 49.962

6.  Rod photoreceptor neurite sprouting in retinitis pigmentosa.

Authors:  Z Y Li; I J Kljavin; A H Milam
Journal:  J Neurosci       Date:  1995-08       Impact factor: 6.167

7.  Mutation analysis of the mouse myosin VIIA deafness gene.

Authors:  P Mburu; X Z Liu; J Walsh; D Saw; M J Cope; F Gibson; J Kendrick-Jones; K P Steel; S D Brown
Journal:  Genes Funct       Date:  1997-06

8.  Localization of kinesin superfamily proteins to the connecting cilium of fish photoreceptors.

Authors:  P L Beech; K Pagh-Roehl; Y Noda; N Hirokawa; B Burnside; J L Rosenbaum
Journal:  J Cell Sci       Date:  1996-04       Impact factor: 5.285

9.  The renewal of photoreceptor cell outer segments.

Authors:  R W Young
Journal:  J Cell Biol       Date:  1967-04       Impact factor: 10.539

10.  Immunocytochemical localization of opsin in the cell membrane of developing rat retinal photoreceptors.

Authors:  I Nir; D Cohen; D S Papermaster
Journal:  J Cell Biol       Date:  1984-05       Impact factor: 10.539

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  120 in total

1.  Calcium-dependent assembly of centrin-G-protein complex in photoreceptor cells.

Authors:  Alexander Pulvermüller; Andreas Giessl; Martin Heck; Ralf Wottrich; Angelika Schmitt; Oliver Peter Ernst; Hui-Woog Choe; Klaus Peter Hofmann; Uwe Wolfrum
Journal:  Mol Cell Biol       Date:  2002-04       Impact factor: 4.272

Review 2.  Photoreceptor renewal: a role for peripherin/rds.

Authors:  Kathleen Boesze-Battaglia; Andrew F X Goldberg
Journal:  Int Rev Cytol       Date:  2002

Review 3.  The many different cellular functions of MYO7A in the retina.

Authors:  David S Williams; Vanda S Lopes
Journal:  Biochem Soc Trans       Date:  2011-10       Impact factor: 5.407

4.  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.

Authors:  Bo Chang; Hemant Khanna; Norman Hawes; David Jimeno; Shirley He; Concepcion Lillo; Sunil K Parapuram; Hong Cheng; Alison Scott; Ron E Hurd; John A Sayer; Edgar A Otto; Massimo Attanasio; John F O'Toole; Genglin Jin; Chengchao Shou; Friedhelm Hildebrandt; David S Williams; John R Heckenlively; Anand Swaroop
Journal:  Hum Mol Genet       Date:  2006-04-21       Impact factor: 6.150

5.  Phosphoinositides, ezrin/moesin, and rac1 regulate fusion of rhodopsin transport carriers in retinal photoreceptors.

Authors:  Dusanka Deretic; Valerie Traverso; Nilda Parkins; Fannie Jackson; Elena B Rodriguez de Turco; Nancy Ransom
Journal:  Mol Biol Cell       Date:  2003-09-17       Impact factor: 4.138

6.  A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26).

Authors:  E van Wijk; E Krieger; M H Kemperman; E M R De Leenheer; P L M Huygen; C W R J Cremers; F P M Cremers; H Kremer
Journal:  J Med Genet       Date:  2003-12       Impact factor: 6.318

7.  Role of myosin VIIa and Rab27a in the motility and localization of RPE melanosomes.

Authors:  Daniel Gibbs; Sassan M Azarian; Concepcion Lillo; Junko Kitamoto; Adriana E Klomp; Karen P Steel; Richard T Libby; David S Williams
Journal:  J Cell Sci       Date:  2004-11-30       Impact factor: 5.285

8.  Photoreceptors in whirler mice show defective transducin translocation and are susceptible to short-term light/dark changes-induced degeneration.

Authors:  Mei Tian; Weimin Wang; Duane Delimont; Linda Cheung; Marisa Zallocchi; Dominic Cosgrove; You-Wei Peng
Journal:  Exp Eye Res       Date:  2013-11-07       Impact factor: 3.467

Review 9.  Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.

Authors:  Pranav Mathur; Jun Yang
Journal:  Biochim Biophys Acta       Date:  2014-12-04

10.  A novel allele of myosin VIIa reveals a critical function for the C-terminal FERM domain for melanosome transport in retinal pigment epithelial cells.

Authors:  Martin Schwander; Vanda Lopes; Anna Sczaniecka; Daniel Gibbs; Concepcion Lillo; David Delano; Lisa M Tarantino; Tim Wiltshire; David S Williams; Ulrich Müller
Journal:  J Neurosci       Date:  2009-12-16       Impact factor: 6.167

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