Literature DB >> 18344445

Genetic modifiers of retinal degeneration in the rd3 mouse.

Michael Danciger1, Diego Ogando, Haidong Yang, Michael T Matthes, Nicole Yu, Kelly Ahern, Douglas Yasumura, Robert W Williams, Matthew M Lavail.   

Abstract

PURPOSE: In previous studies of light-induced (LRD) and age-related (ageRD) retinal degeneration (RD) between the BALB/cByJ (BALB) and B6(Cg)-Tyr(c-2J)/J (B6a) albino mouse strains, RD-modifying quantitative trait loci (QTLs) were identified. After breeding BALB- and B6a-rd3/rd3 congenic strains and finding significant differences in RD, an F1 intercross to determine rd3 QTLs that influence this inherited RD was performed.
METHODS: N10, F2 BALB- and B6a-rd3/rd3 strains were measured for retinal outer nuclear layer (ONL) thickness from 5 to 12 weeks of age. Since 10 weeks showed significant differences in the ONL, F2 progeny from an F1 intercross were measured for ONL thickness. F2 DNAs were genotyped for SNPs by the Center for Inherited Disease Research. Correlation of genotype with phenotype was made with Map Manager QTX.
RESULTS: One hundred forty-eight SNPs approximately 10 cM apart were typed in the F2 progeny and analyzed. Significant QTLs were identified on chromosomes (Chrs) 17, 8, 14, and 6 (B6a alleles protective) and two on Chr 5 (BALB alleles protective). Suggestive QTLs were found as well. For the strongest QTLs, follow-up SNPs were analyzed to narrow the critical intervals. Additional studies demonstrated that rd3 disease is exacerbated by light but not protected by the absence of rhodopsin regeneration.
CONCLUSIONS: QTLs were identified that modulate rd3-RD. These overlapped some QTLs from previous ageRD and LRD studies. The presence of some of the same QTLs in several studies suggests partial commonality in RD pathways. Identifying natural gene/alleles that modify RDs opens avenues of study that may lead to therapies for RD diseases.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18344445      PMCID: PMC2574750          DOI: 10.1167/iovs.08-1715

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


  33 in total

1.  Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele.

Authors:  T L McGee; M Devoto; J Ott; E L Berson; T P Dryja
Journal:  Am J Hum Genet       Date:  1997-11       Impact factor: 11.025

Review 2.  Molecular mechanisms of light-induced photoreceptor apoptosis and neuroprotection for retinal degeneration.

Authors:  Andreas Wenzel; Christian Grimm; Marijana Samardzija; Charlotte E Remé
Journal:  Prog Retin Eye Res       Date:  2004-11-11       Impact factor: 21.198

Review 3.  Mouse models of age-related macular degeneration.

Authors:  P Elizabeth Rakoczy; Meaghan J T Yu; Steven Nusinowitz; Bo Chang; John R Heckenlively
Journal:  Exp Eye Res       Date:  2005-12-01       Impact factor: 3.467

4.  Genetic mapping of RP1 on 8q11-q21 in an Australian family with autosomal dominant retinitis pigmentosa reduces the critical region to 4 cM between D8S601 and D8S285.

Authors:  S Y Xu; M Denton; L Sullivan; S P Daiger; A Gal
Journal:  Hum Genet       Date:  1996-12       Impact factor: 4.132

5.  Arrestin gene mutations in autosomal recessive retinitis pigmentosa.

Authors:  M Nakazawa; Y Wada; M Tamai
Journal:  Arch Ophthalmol       Date:  1998-04

6.  New mouse primary retinal degeneration (rd-3).

Authors:  B Chang; J R Heckenlively; N L Hawes; T H Roderick
Journal:  Genomics       Date:  1993-04       Impact factor: 5.736

7.  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

8.  Rpe65 as a modifier gene for inherited retinal degeneration.

Authors:  M Samardzija; A Wenzel; M Naash; C E Remé; C Grimm
Journal:  Eur J Neurosci       Date:  2006-02       Impact factor: 3.386

9.  Morphological characterization of the retinal degeneration in three strains of mice carrying the rd-3 mutation.

Authors:  Kenneth A Linberg; Robert N Fariss; John R Heckenlively; Debora B Farber; Steven K Fisher
Journal:  Vis Neurosci       Date:  2005 Nov-Dec       Impact factor: 3.241

10.  A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.

Authors:  C F Inglehearn; S A Carter; T J Keen; J Lindsey; A M Stephenson; R Bashir; M al-Maghtheh; A T Moore; M Jay; A C Bird
Journal:  Nat Genet       Date:  1993-05       Impact factor: 38.330

View more
  16 in total

1.  Cone photoreceptor packing density and the outer nuclear layer thickness in healthy subjects.

Authors:  Toco Y P Chui; Hongxin Song; Christopher A Clark; Joel A Papay; Stephen A Burns; Ann E Elsner
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-06-14       Impact factor: 4.799

2.  Genetic modifier loci of mouse Mfrp(rd6) identified by quantitative trait locus analysis.

Authors:  Jungyeon Won; Jeremy R Charette; Vivek M Philip; Timothy M Stearns; Weidong Zhang; Jürgen K Naggert; Mark P Krebs; Patsy M Nishina
Journal:  Exp Eye Res       Date:  2013-11-04       Impact factor: 3.467

Review 3.  Genetic modifiers and oligogenic inheritance.

Authors:  Maria Kousi; Nicholas Katsanis
Journal:  Cold Spring Harb Perspect Med       Date:  2015-06-01       Impact factor: 6.915

4.  Application of quantitative trait locus mapping and transcriptomics to studies of the senescence-accelerated phenotype in rats.

Authors:  Elena E Korbolina; Nikita I Ershov; Leonid O Bryzgalov; Natalia G Kolosova
Journal:  BMC Genomics       Date:  2014-12-19       Impact factor: 3.969

Review 5.  Genetic modifiers as relevant biological variables of eye disorders.

Authors:  Kacie J Meyer; Michael G Anderson
Journal:  Hum Mol Genet       Date:  2017-08-01       Impact factor: 6.150

6.  Retinal degeneration 3 (RD3) protein inhibits catalytic activity of retinal membrane guanylyl cyclase (RetGC) and its stimulation by activating proteins.

Authors:  Igor V Peshenko; Elena V Olshevskaya; Seifollah Azadi; Laurie L Molday; Robert S Molday; Alexander M Dizhoor
Journal:  Biochemistry       Date:  2011-10-11       Impact factor: 3.162

7.  An allele of microtubule-associated protein 1A (Mtap1a) reduces photoreceptor degeneration in Tulp1 and Tub Mutant Mice.

Authors:  Dennis M Maddox; Sakae Ikeda; Akihiro Ikeda; Weidong Zhang; Mark P Krebs; Patsy M Nishina; Jürgen K Naggert
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-03-26       Impact factor: 4.799

8.  Photoreceptor layer topography in children with leber congenital amaurosis caused by RPE65 mutations.

Authors:  Samuel G Jacobson; Artur V Cideciyan; Tomas S Aleman; Alexander Sumaroka; Elizabeth A M Windsor; Sharon B Schwartz; Elise Heon; Edwin M Stone
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-06-06       Impact factor: 4.799

9.  The severity of retinal degeneration in Rp1h gene-targeted mice is dependent on genetic background.

Authors:  Qin Liu; Alexei Saveliev; Eric A Pierce
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-12-05       Impact factor: 4.799

10.  Changes in gene expression associated with retinal degeneration in the rd3 mouse.

Authors:  Christiana L Cheng; Robert S Molday
Journal:  Mol Vis       Date:  2013-05-06       Impact factor: 2.367

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.