Literature DB >> 11773008

Identification and subcellular localization of the RP1 protein in human and mouse photoreceptors.

Qin Liu1, Jie Zhou, Stephen P Daiger, Debora B Farber, John R Heckenlively, Julie E Smith, Lori S Sullivan, Jian Zuo, Ann H Milam, Eric A Pierce.   

Abstract

PURPOSE: Mutations in the RP1 gene account for 6% to 10% of autosomal dominant retinitis pigmentosa (adRP). Previous studies have shown that the RP1 gene is expressed specifically in photoreceptor cells. So far, little is known about the RP1 protein or how mutations in RP1 lead to photoreceptor cell death. The goal of this study was to identify the RP1 protein and investigate its location in photoreceptor cells.
METHODS: A combination of RT-PCR and rapid amplification of cDNA ends (RACE) was used to isolate the full-length mouse Rp1 cDNA. Antibodies against different regions of the predicted mouse Rp1 protein were generated. Western blot analyses were used to identify the RP1/Rp1 proteins. The subcellular location of RP1 in human and mouse retinas was determined by immunostaining retinal sections.
RESULTS: The full-length mouse Rp1 cDNA is 6944 bp, encoding a predicted protein of 2095 amino acids. Rp1 was found to be a soluble protein of approximately 240 kDa, consistent with predictions based on the cDNA sequence. Immunofluorescence analyses revealed that both the human RP1 and mouse Rp1 proteins are specifically localized in the connecting cilia of rod and cone photoreceptors.
CONCLUSIONS: The presence of RP1/Rp1 in connecting cilia suggests that it may participate in transport of proteins between the inner and outer segments of photoreceptors or in maintenance of cilial structure. This study forms the basis for further investigation of the function of RP1 in retina and the mechanism by which mutations in RP1 lead to photoreceptor cell death.

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Year:  2002        PMID: 11773008      PMCID: PMC1963488     

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  51 in total

1.  Genetic evidence for selective transport of opsin and arrestin by kinesin-II in mammalian photoreceptors.

Authors:  J R Marszalek; X Liu; E A Roberts; D Chui; J D Marth; D S Williams; L S Goldstein
Journal:  Cell       Date:  2000-07-21       Impact factor: 41.582

2.  RP1 protein truncating mutations predominate at the RP1 adRP locus.

Authors:  A Payne; E Vithana; S Khaliq; A Hameed; J Deller; L Abu-Safieh; S Kermani; B P Leroy; S Q Mehdi; A T Moore; A C Bird; S S Bhattacharya
Journal:  Invest Ophthalmol Vis Sci       Date:  2000-12       Impact factor: 4.799

3.  The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors.

Authors:  R Roepman; N Bernoud-Hubac; D E Schick; A Maugeri; W Berger; H H Ropers; F P Cremers; P A Ferreira
Journal:  Hum Mol Genet       Date:  2000-09-01       Impact factor: 6.150

4.  Cone properties of retinal margin cells in the monkey (Macaca mulatta).

Authors:  X Chen; K C Wikler; P R MacLeish
Journal:  Invest Ophthalmol Vis Sci       Date:  2000-07       Impact factor: 4.799

5.  Rhodopsin transport in the membrane of the connecting cilium of mammalian photoreceptor cells.

Authors:  U Wolfrum; A Schmitt
Journal:  Cell Motil Cytoskeleton       Date:  2000-06

6.  Patient mutations in doublecortin define a repeated tubulin-binding domain.

Authors:  K R Taylor; A K Holzer; J F Bazan; C A Walsh; J G Gleeson
Journal:  J Biol Chem       Date:  2000-11-03       Impact factor: 5.157

7.  DCAMKL1 encodes a protein kinase with homology to doublecortin that regulates microtubule polymerization.

Authors:  P T Lin; J G Gleeson; J C Corbo; L Flanagan; C A Walsh
Journal:  J Neurosci       Date:  2000-12-15       Impact factor: 6.167

8.  Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa.

Authors:  S J Bowne; S P Daiger; M M Hims; M M Sohocki; K A Malone; A B McKie; J R Heckenlively; D G Birch; C F Inglehearn; S S Bhattacharya; A Bird; L S Sullivan
Journal:  Hum Mol Genet       Date:  1999-10       Impact factor: 6.150

Review 9.  Rhodopsin trafficking and its role in retinal dystrophies.

Authors:  C H Sung; A W Tai
Journal:  Int Rev Cytol       Date:  2000

10.  A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model for X-linked retinitis pigmentosa (RP3).

Authors:  D H Hong; B S Pawlyk; J Shang; M A Sandberg; E L Berson; T Li
Journal:  Proc Natl Acad Sci U S A       Date:  2000-03-28       Impact factor: 11.205

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  52 in total

Review 1.  Photoreceptor sensory cilia and inherited retinal degeneration.

Authors:  Qin Liu; Qi Zhang; Eric A Pierce
Journal:  Adv Exp Med Biol       Date:  2010       Impact factor: 2.622

Review 2.  Pre-mRNA splicing and retinitis pigmentosa.

Authors:  Daniel Mordes; Xiaoyan Luo; Amar Kar; David Kuo; Lili Xu; Kazuo Fushimi; Guowu Yu; Paul Sternberg; Jane Y Wu
Journal:  Mol Vis       Date:  2006-10-26       Impact factor: 2.367

3.  Evaluation of the 17-kDa prenyl-binding protein as a regulatory protein for phototransduction in retinal photoreceptors.

Authors:  Angela W Norton; Suzanne Hosier; Jennifer M Terew; Ning Li; Anuradha Dhingra; Noga Vardi; Wolfgang Baehr; Rick H Cote
Journal:  J Biol Chem       Date:  2004-10-25       Impact factor: 5.157

Review 4.  Genetic factors modifying clinical expression of autosomal dominant RP.

Authors:  Stephen P Daiger; Suma P Shankar; Alice B Schindler; Lori S Sullivan; Sara J Bowne; Terri M King; E Warick Daw; Edwin M Stone; John R Heckenlively
Journal:  Adv Exp Med Biol       Date:  2006       Impact factor: 2.622

5.  A genomewide scan for age-related macular degeneration provides evidence for linkage to several chromosomal regions.

Authors:  Johanna M Seddon; Susan L Santangelo; Kathryn Book; Sandy Chong; Jennifer Cote
Journal:  Am J Hum Genet       Date:  2003-08-22       Impact factor: 11.025

6.  Identification of a novel p.R1443W mutation in RP1 gene associated with retinitis pigmentosa sine pigmento.

Authors:  Li Ma; Xun-Lun Sheng; Hui-Ping Li; Fang-Xia Zhang; Ya-Ni Liu; Wei-Ning Rong; Jian-Ling Zhang
Journal:  Int J Ophthalmol       Date:  2013-08-18       Impact factor: 1.779

Review 7.  Genetic characterization and disease mechanism of retinitis pigmentosa; current scenario.

Authors:  Muhammad Umar Ali; Muhammad Saif Ur Rahman; Jiang Cao; Ping Xi Yuan
Journal:  3 Biotech       Date:  2017-07-18       Impact factor: 2.406

8.  Deletion of both centrin 2 (CETN2) and CETN3 destabilizes the distal connecting cilium of mouse photoreceptors.

Authors:  Guoxin Ying; Jeanne M Frederick; Wolfgang Baehr
Journal:  J Biol Chem       Date:  2019-01-15       Impact factor: 5.157

9.  Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein.

Authors:  Erwin van Wijk; Ferry F J Kersten; Aileen Kartono; Dorus A Mans; Kim Brandwijk; Stef J F Letteboer; Theo A Peters; Tina Märker; Xiumin Yan; Cor W R J Cremers; Frans P M Cremers; Uwe Wolfrum; Ronald Roepman; Hannie Kremer
Journal:  Hum Mol Genet       Date:  2008-09-30       Impact factor: 6.150

10.  The dynamic cilium in human diseases.

Authors:  Anna D'Angelo; Brunella Franco
Journal:  Pathogenetics       Date:  2009-05-13
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