Literature DB >> 22323458

RpgrORF15 connects to the usher protein network through direct interactions with multiple whirlin isoforms.

Rachel N Wright1, Dong-Hyun Hong, Brian Perkins.   

Abstract

PURPOSE: Mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene are a frequent cause of X-linked retinitis pigmentosa. The RPGR transcript undergoes complex alternative splicing to express both constitutive (Rpgr(ex1-19)) and Rpgr(ORF15) variants. Because functional studies of Rpgr suggest a role in intracellular protein trafficking through the connecting cilia, the goal of this study was to identify potential binding partners for Rpgr(ORF15) and to identify the domains on whirlin necessary for Rpgr binding.
METHODS: The C-terminus of mouse Rpgr(ORF15) was used as bait in a yeast two-hybrid system. Whirlin expression was analyzed using RT-PCR and Western blot analysis. Protein-protein interactions were confirmed using in vitro binding assays and coimmunoprecipitation. Subcellular colocalization was analyzed using immunohistochemistry on retinal cryosections.
RESULTS: Yeast two-hybrid analysis identified whirlin, a PDZ-scaffold protein, as a putative binding partner for Rpgr(ORF15). The RPGR(ORF15)-whirlin interaction was confirmed using in vitro binding assays and coimmunoprecipitation from retinal tissue, and both proteins were shown to colocalize in the photoreceptor connecting cilia in vivo. Results from RT-PCR, Western blot analysis, and immunocytochemistry demonstrated that whirlin expressed multiple isoforms in photoreceptors with variable subcellular localization.
CONCLUSIONS: Whirlin expression has been reported in photoreceptors and cochlear hair cells, and mutations in whirlin cause Usher syndrome (USH2D) and nonsyndromic congenital deafness (DFNB31). Because mutations in the 5' end of whirlin are associated with the syndromic phenotype associated with USH2D, the identification of novel N-terminal isoforms in the retina and a novel RPGR(ORF15)-whirlin interaction provide a potential mechanism for the retinal phenotype observed in USH2D.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22323458      PMCID: PMC3339914          DOI: 10.1167/iovs.11-8845

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


  36 in total

1.  Rod and cone responses in sex-linked retinitis pigmentosa.

Authors:  E L Berson; P Gouras; R D Gunkel; N C Myrianthopoulos
Journal:  Arch Ophthalmol       Date:  1969-02

2.  Usher syndrome: definition and estimate of prevalence from two high-risk populations.

Authors:  J A Boughman; M Vernon; K A Shaver
Journal:  J Chronic Dis       Date:  1983

3.  DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.

Authors:  Mirna Mustapha; Eliane Chouery; Sébastien Chardenoux; Mohamed Naboulsi; Joël Paronnaud; Arnaud Lemainque; André Mégarbané; Jacques Loiselet; Dominique Weil; Mark Lathrop; Christine Petit
Journal:  Eur J Hum Genet       Date:  2002-03       Impact factor: 4.246

4.  Different RPGR exon ORF15 mutations in Canids provide insights into photoreceptor cell degeneration.

Authors:  Qi Zhang; Gregory M Acland; Wen X Wu; Jennifer L Johnson; Sue Pearce-Kelling; Brian Tulloch; Raf Vervoort; Alan F Wright; Gustavo D Aguirre
Journal:  Hum Mol Genet       Date:  2002-05-01       Impact factor: 6.150

5.  Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.

Authors:  Philomena Mburu; Mirna Mustapha; Anabel Varela; Dominique Weil; Aziz El-Amraoui; Ralph H Holme; Andreas Rump; Rachel E Hardisty; Stéphane Blanchard; Roney S Coimbra; Isabelle Perfettini; Nick Parkinson; Ann-Marie Mallon; Pete Glenister; Mike J Rogers; Adam J Paige; Lee Moir; Jo Clay; Andre Rosenthal; Xue Zhong Liu; Gonzalo Blanco; Karen P Steel; Christine Petit; Steve D M Brown
Journal:  Nat Genet       Date:  2003-08       Impact factor: 38.330

6.  Prevalence of retinitis pigmentosa in Maine.

Authors:  C H Bunker; E L Berson; W C Bromley; R P Hayes; T H Roderick
Journal:  Am J Ophthalmol       Date:  1984-03       Impact factor: 5.258

7.  RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa.

Authors:  Dror Sharon; Michael A Sandberg; Vivian W Rabe; Melissa Stillberger; Thaddeus P Dryja; Eliot L Berson
Journal:  Am J Hum Genet       Date:  2003-10-16       Impact factor: 11.025

8.  RPGR isoforms in photoreceptor connecting cilia and the transitional zone of motile cilia.

Authors:  Dong-Hyun Hong; Basil Pawlyk; Maxim Sokolov; Katherine J Strissel; Jun Yang; Brian Tulloch; Alan F Wright; Vadim Y Arshavsky; Tiansen Li
Journal:  Invest Ophthalmol Vis Sci       Date:  2003-06       Impact factor: 4.799

9.  The retinitis pigmentosa GTPase regulator (RPGR)- interacting protein: subserving RPGR function and participating in disk morphogenesis.

Authors:  Yun Zhao; Dong-Hyun Hong; Basil Pawlyk; Guohua Yue; Michael Adamian; Marcin Grynberg; Adam Godzik; Tiansen Li
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-21       Impact factor: 11.205

10.  Rootletin, a novel coiled-coil protein, is a structural component of the ciliary rootlet.

Authors:  Jun Yang; Xiaoqing Liu; Guohua Yue; Michael Adamian; Oleg Bulgakov; Tiansen Li
Journal:  J Cell Biol       Date:  2002-11-11       Impact factor: 10.539

View more
  26 in total

1.  Disruption of RPGR protein interaction network is the common feature of RPGR missense variations that cause XLRP.

Authors:  Qihong Zhang; Joseph C Giacalone; Charles Searby; Edwin M Stone; Budd A Tucker; Val C Sheffield
Journal:  Proc Natl Acad Sci U S A       Date:  2019-01-08       Impact factor: 11.205

Review 2.  Usher syndrome and non-syndromic deafness: Functions of different whirlin isoforms in the cochlea, vestibular organs, and retina.

Authors:  Pranav Dinesh Mathur; Jun Yang
Journal:  Hear Res       Date:  2019-02-22       Impact factor: 3.208

3.  Whirlin increases TRPV1 channel expression and cellular stability.

Authors:  Maria Grazia Ciardo; Amparo Andrés-Bordería; Natalia Cuesta; Pierluigi Valente; María Camprubí-Robles; Jun Yang; Rosa Planells-Cases; Antonio Ferrer-Montiel
Journal:  Biochim Biophys Acta       Date:  2015-10-26

Review 4.  Gene augmentation for X-linked retinitis pigmentosa caused by mutations in RPGR.

Authors:  William A Beltran; Artur V Cideciyan; Alfred S Lewin; William W Hauswirth; Samuel G Jacobson; Gustavo D Aguirre
Journal:  Cold Spring Harb Perspect Med       Date:  2014-10-09       Impact factor: 6.915

5.  Development of a Molecularly Stable Gene Therapy Vector for the Treatment of RPGR-Associated X-Linked Retinitis Pigmentosa.

Authors:  Joseph C Giacalone; Jeaneen L Andorf; Qihong Zhang; Erin R Burnight; Dalyz Ochoa; Austin J Reutzel; Malia M Collins; Val C Sheffield; Robert F Mullins; Ian C Han; Edwin M Stone; Budd A Tucker
Journal:  Hum Gene Ther       Date:  2019-08       Impact factor: 5.695

6.  A study of whirlin isoforms in the mouse vestibular system suggests potential vestibular dysfunction in DFNB31-deficient patients.

Authors:  Pranav Dinesh Mathur; Sarath Vijayakumar; Deepti Vashist; Sherri M Jones; Timothy A Jones; Jun Yang
Journal:  Hum Mol Genet       Date:  2015-09-29       Impact factor: 6.150

Review 7.  Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.

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

8.  CEP78 is mutated in a distinct type of Usher syndrome.

Authors:  Qing Fu; Mingchu Xu; Xue Chen; Xunlun Sheng; Zhisheng Yuan; Yani Liu; Huajin Li; Zixi Sun; Huiping Li; Lizhu Yang; Keqing Wang; Fangxia Zhang; Yumei Li; Chen Zhao; Ruifang Sui; Rui Chen
Journal:  J Med Genet       Date:  2016-09-14       Impact factor: 6.318

Review 9.  Usher protein functions in hair cells and photoreceptors.

Authors:  Dominic Cosgrove; Marisa Zallocchi
Journal:  Int J Biochem Cell Biol       Date:  2013-11-12       Impact factor: 5.085

10.  Distinct expression and function of whirlin isoforms in the inner ear and retina: an insight into pathogenesis of USH2D and DFNB31.

Authors:  Pranav Dinesh Mathur; Junhuang Zou; Tihua Zheng; Ali Almishaal; Yong Wang; Qian Chen; Le Wang; Deepti Vashist; Steve Brown; Albert Park; Jun Yang
Journal:  Hum Mol Genet       Date:  2015-08-24       Impact factor: 6.150

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.