Literature DB >> 23778877

Complementation test of Rpe65 knockout and tvrm148.

Charles B Wright1, Micah A Chrenek, Stephanie L Foster, Todd Duncan, T Michael Redmond, Machelle T Pardue, Jeffrey H Boatright, John M Nickerson.   

Abstract

PURPOSE: A mouse mutation, tvrm148, was previously reported as resulting in retinal degeneration. Tvrm148 and Rpe65 map between markers D3Mit147 and D3Mit19 on a genetic map, but the physical map places RPE65 outside the markers. We asked if Rpe65 or perhaps another nearby gene is mutated and if the mutant reduced 11-cis-retinal levels. We studied the impact of the tvrm148 mutation on visual function, morphology, and retinoid levels.
METHODS: Normal phase HPLC was used to measure retinoid levels. Rpe65(+/+), tvrm148/+ (T(+/-)), tvrm148/tvrm148 (T(-/-)), RPE65(KO/KO) (Rpe65(-/-)), and Rpe65(T/-) mice visual function was measured by optokinetic tracking (OKT) and electroretinography (ERG). Morphology was assessed by light microscopy and transmission electron microscopy (TEM). qRT-PCR was used to measure Rpe65 mRNA levels. Immunoblotting measured the size and amount of RPE65 protein.
RESULTS: The knockout and tvrm148 alleles did not complement. No 11-cis-retinal was detected in T(-/-) or Rpe65(-/-) mice. Visual acuity in Rpe65(+/+) and T(+/-) mouse was -0.382 c/d, but 0.037 c/d in T(-/-) mice at postnatal day 210 (P210). ERG response in T(-/-) mice was undetectable except at bright flash intensities. Outer nuclear layer (ONL) thickness in T(-/-) mice was -70% of Rpe65(+/+) by P210. Rpe65 mRNA levels in T(-/-) mice were unchanged, yet 14.5% of Rpe65(+/+) protein levels was detected. Protein size was unchanged.
CONCLUSIONS: A complementation test revealed the RPE65 knockout and tvrm148 alleles do not complement, proving that the tvrm148 mutation is in Rpe65. Behavioral, physiological, molecular, biochemical, and histological approaches indicate that tvrm148 is a null allele of Rpe65.

Entities:  

Keywords:  RPE65/Rpe65; mutation; visual cycle

Mesh:

Substances:

Year:  2013        PMID: 23778877      PMCID: PMC3729239          DOI: 10.1167/iovs.13-12336

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


  70 in total

1.  Retinal disease in Rpe65-deficient mice: comparison to human leber congenital amaurosis due to RPE65 mutations.

Authors:  Rafael C Caruso; Tomas S Aleman; Artur V Cideciyan; Alejandro J Roman; Alexander Sumaroka; Cristina L Mullins; Sanford L Boye; William W Hauswirth; Samuel G Jacobson
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-05-19       Impact factor: 4.799

2.  Impacts of two point mutations of RPE65 from Leber's congenital amaurosis on the stability, subcellular localization and isomerohydrolase activity of RPE65.

Authors:  Ying Chen; Gennadiy Moiseyev; Yusuke Takahashi; Jian-Xing Ma
Journal:  FEBS Lett       Date:  2006-07-05       Impact factor: 4.124

3.  Rods and cones in the mouse retina. I. Structural analysis using light and electron microscopy.

Authors:  L D Carter-Dawson; M M LaVail
Journal:  J Comp Neurol       Date:  1979-11-15       Impact factor: 3.215

4.  Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).

Authors:  Ji-Jing Pang; Bo Chang; Norman L Hawes; Ronald E Hurd; Muriel T Davisson; Jie Li; Syed M Noorwez; Ritu Malhotra; J Hugh McDowell; Shalesh Kaushal; William W Hauswirth; Steven Nusinowitz; Debra A Thompson; John R Heckenlively
Journal:  Mol Vis       Date:  2005-02-28       Impact factor: 2.367

Review 5.  The cone-specific visual cycle.

Authors:  Jin-Shan Wang; Vladimir J Kefalov
Journal:  Prog Retin Eye Res       Date:  2010-11-25       Impact factor: 21.198

6.  Remaining rod activity mediates visual behavior in adult Rpe65-/- mice.

Authors:  Maité Cachafeiro; Alexis-Pierre Bemelmans; Kriss Canola; Vérène Pignat; Sylvain Vincent Crippa; Corinne Kostic; Yvan Arsenijevic
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-08-11       Impact factor: 4.799

7.  Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.

Authors:  B Chang; N L Hawes; M T Pardue; A M German; R E Hurd; M T Davisson; S Nusinowitz; K Rengarajan; A P Boyd; S S Sidney; M J Phillips; R E Stewart; R Chaudhury; J M Nickerson; J R Heckenlively; J H Boatright
Journal:  Vision Res       Date:  2007-01-30       Impact factor: 1.886

8.  Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis.

Authors:  H Morimura; G A Fishman; S A Grover; A B Fulton; E L Berson; T P Dryja
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-17       Impact factor: 11.205

9.  Defining the residual vision in leber congenital amaurosis caused by RPE65 mutations.

Authors:  Samuel G Jacobson; Tomas S Aleman; Artur V Cideciyan; Alejandro J Roman; Alexander Sumaroka; Elizabeth A M Windsor; Sharon B Schwartz; Elise Heon; Edwin M Stone
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-12-30       Impact factor: 4.799

10.  SNAP: predict effect of non-synonymous polymorphisms on function.

Authors:  Yana Bromberg; Burkhard Rost
Journal:  Nucleic Acids Res       Date:  2007-05-25       Impact factor: 16.971

View more
  9 in total

Review 1.  Psychophysical testing in rodent models of glaucomatous optic neuropathy.

Authors:  Stephanie L Grillo; Peter Koulen
Journal:  Exp Eye Res       Date:  2015-07-02       Impact factor: 3.467

2.  Inverse correlation between fatty acid transport protein 4 and vision in Leber congenital amaurosis associated with RPE65 mutation.

Authors:  Songhua Li; William C Gordon; Nicolas G Bazan; Minghao Jin
Journal:  Proc Natl Acad Sci U S A       Date:  2020-11-30       Impact factor: 11.205

3.  Visual Cone Arrestin 4 Contributes to Visual Function and Cone Health.

Authors:  Janise D Deming; Joseph S Pak; Bruce M Brown; Moon K Kim; Moe H Aung; Yun Sung Eom; Jung-A Shin; Eun-Jin Lee; Machelle T Pardue; Cheryl Mae Craft
Journal:  Invest Ophthalmol Vis Sci       Date:  2015-08       Impact factor: 4.799

4.  Temperature-sensitive retinoid isomerase activity of RPE65 mutants associated with Leber Congenital Amaurosis.

Authors:  Songhua Li; Jane Hu; Robin J Jin; Ashok Aiyar; Samuel G Jacobson; Dean Bok; Minghao Jin
Journal:  J Biochem       Date:  2015-03-09       Impact factor: 3.387

5.  Pharmacological Amelioration of Cone Survival and Vision in a Mouse Model for Leber Congenital Amaurosis.

Authors:  Songhua Li; Marijana Samardzija; Zhihui Yang; Christian Grimm; Minghao Jin
Journal:  J Neurosci       Date:  2016-05-25       Impact factor: 6.167

6.  The Rpe65 rd12 allele exerts a semidominant negative effect on vision in mice.

Authors:  Charles B Wright; Micah A Chrenek; Wei Feng; Shannon E Getz; Todd Duncan; Machelle T Pardue; Yue Feng; T Michael Redmond; Jeffrey H Boatright; John M Nickerson
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-04-17       Impact factor: 4.799

7.  Rescue of enzymatic function for disease-associated RPE65 proteins containing various missense mutations in non-active sites.

Authors:  Songhua Li; Tadahide Izumi; Jane Hu; Heather H Jin; Ahmed-Abdul A Siddiqui; Samuel G Jacobson; Dean Bok; Minghao Jin
Journal:  J Biol Chem       Date:  2014-05-21       Impact factor: 5.157

8.  IRBP deficiency permits precocious ocular development and myopia.

Authors:  Shanu Markand; Natecia L Baskin; Ranjay Chakraborty; Erica Landis; Sara A Wetzstein; Kevin J Donaldson; Priyanka Priyadarshani; Shannon E Alderson; Curran S Sidhu; Jeffrey H Boatright; P Michael Iuvone; Machelle T Pardue; John M Nickerson
Journal:  Mol Vis       Date:  2016-10-27       Impact factor: 2.367

9.  The Lrat-/- Rat: CRISPR/Cas9 Construction and Phenotyping of a New Animal Model for Retinitis Pigmentosa.

Authors:  Céline Koster; Koen T van den Hurk; Colby F Lewallen; Mays Talib; Jacoline B Ten Brink; Camiel J F Boon; Arthur A Bergen
Journal:  Int J Mol Sci       Date:  2021-07-05       Impact factor: 5.923

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.