Literature DB >> 28289063

Photoreceptor Cilia and Retinal Ciliopathies.

Kinga M Bujakowska1, Qin Liu1, Eric A Pierce1.   

Abstract

Photoreceptors are sensory neurons designed to convert light stimuli into neurological responses. This process, called phototransduction, takes place in the outer segments (OS) of rod and cone photoreceptors. OS are specialized sensory cilia, with analogous structures to those present in other nonmotile cilia. Deficient morphogenesis and/or dysfunction of photoreceptor sensory cilia (PSC) caused by mutations in a variety of photoreceptor-specific and common cilia genes can lead to inherited retinal degenerations (IRDs). IRDs can manifest as isolated retinal diseases or syndromic diseases. In this review, we describe the structure and composition of PSC and different forms of ciliopathies with retinal involvement. We review the genetics of the IRDs, which are monogenic disorders but genetically diverse with regard to causality.
Copyright © 2017 Cold Spring Harbor Laboratory Press; all rights reserved.

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Year:  2017        PMID: 28289063      PMCID: PMC5629997          DOI: 10.1101/cshperspect.a028274

Source DB:  PubMed          Journal:  Cold Spring Harb Perspect Biol        ISSN: 1943-0264            Impact factor:   10.005


  311 in total

1.  Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment gene.

Authors:  R Ayyagari; L E Kakuk; C L Coats; E L Bingham; Y Toda; J Felius; P A Sieving
Journal:  Mol Vis       Date:  1999-07-28       Impact factor: 2.367

2.  Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study.

Authors:  A J Hardcastle; D L Thiselton; L Van Maldergem; B K Saha; M Jay; C Plant; R Taylor; A C Bird; S Bhattacharya
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

3.  Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosa.

Authors:  A J Mears; L Gieser; D Yan; C Chen; S Fahrner; S Hiriyanna; R Fujita; S G Jacobson; P A Sieving; A Swaroop
Journal:  Am J Hum Genet       Date:  1999-03       Impact factor: 11.025

4.  Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis.

Authors:  V L Ruiz-Perez; S E Ide; T M Strom; B Lorenz; D Wilson; K Woods; L King; C Francomano; P Freisinger; S Spranger; B Marino; B Dallapiccola; M Wright; T Meitinger; M H Polymeropoulos; J Goodship
Journal:  Nat Genet       Date:  2000-03       Impact factor: 38.330

5.  Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss.

Authors:  C Rivolta; E A Sweklo; E L Berson; T P Dryja
Journal:  Am J Hum Genet       Date:  2000-04-20       Impact factor: 11.025

6.  Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis.

Authors:  G Clarke; A F Goldberg; D Vidgen; L Collins; L Ploder; L Schwarz; L L Molday; J Rossant; A Szél; R S Molday; D G Birch; R R McInnes
Journal:  Nat Genet       Date:  2000-05       Impact factor: 38.330

7.  Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa.

Authors:  E A Pierce; T Quinn; T Meehan; T L McGee; E L Berson; T P Dryja
Journal:  Nat Genet       Date:  1999-07       Impact factor: 38.330

8.  A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration.

Authors:  M A Maw; D Corbeil; J Koch; A Hellwig; J C Wilson-Wheeler; R J Bridges; G Kumaramanickavel; S John; D Nancarrow; K Röper; A Weigmann; W B Huttner; M J Denton
Journal:  Hum Mol Genet       Date:  2000-01-01       Impact factor: 6.150

9.  A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locus.

Authors:  X Guillonneau; N I Piriev; M Danciger; C A Kozak; A V Cideciyan; S G Jacobson; D B Farber
Journal:  Hum Mol Genet       Date:  1999-08       Impact factor: 6.150

10.  Myosin VIIa participates in opsin transport through the photoreceptor cilium.

Authors:  X Liu; I P Udovichenko; S D Brown; K P Steel; D S Williams
Journal:  J Neurosci       Date:  1999-08-01       Impact factor: 6.167

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  53 in total

1.  Ift172 conditional knock-out mice exhibit rapid retinal degeneration and protein trafficking defects.

Authors:  Priya R Gupta; Nachiket Pendse; Scott H Greenwald; Mihoko Leon; Qin Liu; Eric A Pierce; Kinga M Bujakowska
Journal:  Hum Mol Genet       Date:  2018-06-01       Impact factor: 6.150

Review 2.  Photoreceptor outer segment as a sink for membrane proteins: hypothesis and implications in retinal ciliopathies.

Authors:  Seongjin Seo; Poppy Datta
Journal:  Hum Mol Genet       Date:  2017-08-01       Impact factor: 6.150

3.  Limited time window for retinal gene therapy in a preclinical model of ciliopathy.

Authors:  Poppy Datta; Avri Ruffcorn; Seongjin Seo
Journal:  Hum Mol Genet       Date:  2020-08-11       Impact factor: 6.150

4.  Loss of zebrafish dzip1 results in inappropriate recruitment of periocular mesenchyme to the optic fissure and ocular coloboma.

Authors:  Sri Pratima Nandamuri; Sarah Lusk; Kristen M Kwan
Journal:  PLoS One       Date:  2022-03-14       Impact factor: 3.240

Review 5.  Mechanism and Regulation of Centriole and Cilium Biogenesis.

Authors:  David K Breslow; Andrew J Holland
Journal:  Annu Rev Biochem       Date:  2019-01-11       Impact factor: 23.643

6.  WDR34, a candidate gene for non-syndromic rod-cone dystrophy.

Authors:  Maria Solaguren-Beascoa; Kinga M Bujakowska; Cécile Méjécase; Lisa Emmenegger; Elise Orhan; Marion Neuillé; Saddek Mohand-Saïd; Christel Condroyer; Marie-Elise Lancelot; Christelle Michiels; Vanessa Demontant; Aline Antonio; Mélanie Letexier; Jean-Paul Saraiva; Christine Lonjou; Wassila Carpentier; Thierry Léveillard; Eric A Pierce; Hélène Dollfus; José-Alain Sahel; Shomi S Bhattacharya; Isabelle Audo; Christina Zeitz
Journal:  Clin Genet       Date:  2020-11-09       Impact factor: 4.438

7.  The molecular structure of mammalian primary cilia revealed by cryo-electron tomography.

Authors:  Petra Kiesel; Gonzalo Alvarez Viar; Nikolai Tsoy; Riccardo Maraspini; Peter Gorilak; Vladimir Varga; Alf Honigmann; Gaia Pigino
Journal:  Nat Struct Mol Biol       Date:  2020-09-28       Impact factor: 15.369

8.  Multistep peripherin-2/rds self-assembly drives membrane curvature for outer segment disk architecture and photoreceptor viability.

Authors:  Michelle L Milstein; Breyanna L Cavanaugh; Nicole M Roussey; Stefanie Volland; David S Williams; Andrew F X Goldberg
Journal:  Proc Natl Acad Sci U S A       Date:  2020-02-10       Impact factor: 11.205

Review 9.  Cilia in cystic kidney and other diseases.

Authors:  Gregory J Pazour; Lynne Quarmby; Abigail O Smith; Paurav B Desai; Miriam Schmidts
Journal:  Cell Signal       Date:  2019-12-24       Impact factor: 4.315

Review 10.  Dissecting the role of EYS in retinal degeneration: clinical and molecular aspects and its implications for future therapy.

Authors:  Ana B Garcia-Delgado; Lourdes Valdes-Sanchez; Maria Jose Morillo-Sanchez; Beatriz Ponte-Zuñiga; Francisco J Diaz-Corrales; Berta de la Cerda
Journal:  Orphanet J Rare Dis       Date:  2021-05-17       Impact factor: 4.123

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