Literature DB >> 26427412

FAM161A and TTC8 are Differentially Expressed in Non-Allelelic Early Onset Retinal Degeneration.

Louise M Downs1, Gustavo D Aguirre2.   

Abstract

Ciliary genes FAM161A and TTC8 have been implicated in retinal degeneration (RD) in humans and in dogs. The identification of FAM161A and TTC8 mutations in canine RD is exciting as there is the potential to develop novel large animal models for RD. However, the disease phenotypes in the dog and the roles of abnormal genes in disease pathology have yet to be fully characterized. The present study evaluated the expression patterns of FAM161A and TTC8 during normal retinal development in dogs, and in three non-allelic, early onset canine RD models at critical time points of the disease: RCD1, XLPRA2 and ERD. Both genes were differentially expressed in RCD1 and ERD, but not in XLPRA2. These results add evidence to the hypothesis that (a) mutations in many retinal genes have a cascade effect on the expression of multiple, possibly unrelated genes and (b) a large number and wide range of genes probably contribute to RD in general.

Entities:  

Keywords:  Dog model; Expression study; FAM161A; Microtubules; Photoreceptor; Retinal degeneration; TTC8

Mesh:

Substances:

Year:  2016        PMID: 26427412      PMCID: PMC4602411          DOI: 10.1007/978-3-319-17121-0_27

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  22 in total

1.  Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.

Authors:  K J Livak; T D Schmittgen
Journal:  Methods       Date:  2001-12       Impact factor: 3.608

2.  A splice-site mutation in a retina-specific exon of BBS8 causes nonsyndromic retinitis pigmentosa.

Authors:  S Amer Riazuddin; Muhammad Iqbal; Yue Wang; Tomohiro Masuda; Yuhng Chen; Sara Bowne; Lori S Sullivan; Naushin H Waseem; Shomi Bhattacharya; Stephen P Daiger; Kang Zhang; Shaheen N Khan; Sheikh Riazuddin; J Fielding Hejtmancik; Paul A Sieving; Donald J Zack; Nicholas Katsanis
Journal:  Am J Hum Genet       Date:  2010-05-06       Impact factor: 11.025

3.  Degenerations of the dog retina. II. Generalized progressive atrophy of hereditary origin.

Authors:  H B PARRY
Journal:  Br J Ophthalmol       Date:  1953-08       Impact factor: 4.638

4.  Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa.

Authors:  Thomas Langmann; Silvio Alessandro Di Gioia; Isabella Rau; Heidi Stöhr; Nela S Maksimovic; Joseph C Corbo; Agnes B Renner; Eberhart Zrenner; Govindasamy Kumaramanickavel; Marcus Karlstetter; Yvan Arsenijevic; Bernhard H F Weber; Andreas Gal; Carlo Rivolta
Journal:  Am J Hum Genet       Date:  2010-08-12       Impact factor: 11.025

5.  Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa.

Authors:  Dikla Bandah-Rozenfeld; Liliana Mizrahi-Meissonnier; Chen Farhy; Alexey Obolensky; Itay Chowers; Jacob Pe'er; Saul Merin; Tamar Ben-Yosef; Ruth Ashery-Padan; Eyal Banin; Dror Sharon
Journal:  Am J Hum Genet       Date:  2010-08-12       Impact factor: 11.025

6.  Exonic SINE insertion in STK38L causes canine early retinal degeneration (erd).

Authors:  Orly Goldstein; Anna V Kukekova; Gustavo D Aguirre; Gregory M Acland
Journal:  Genomics       Date:  2010-09-29       Impact factor: 5.736

7.  The beta subunit of cyclic GMP phosphodiesterase mRNA is deficient in canine rod-cone dysplasia 1.

Authors:  D B Farber; J S Danciger; G Aguirre
Journal:  Neuron       Date:  1992-08       Impact factor: 17.173

8.  Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit gene.

Authors:  M L Suber; S J Pittler; N Qin; G C Wright; V Holcombe; R H Lee; C M Craft; R N Lolley; W Baehr; R L Hurwitz
Journal:  Proc Natl Acad Sci U S A       Date:  1993-05-01       Impact factor: 11.205

9.  FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies.

Authors:  Silvio Alessandro Di Gioia; Stef J F Letteboer; Corinne Kostic; Dikla Bandah-Rozenfeld; Lisette Hetterschijt; Dror Sharon; Yvan Arsenijevic; Ronald Roepman; Carlo Rivolta
Journal:  Hum Mol Genet       Date:  2012-09-01       Impact factor: 6.150

10.  Photoreceptor cell death, proliferation and formation of hybrid rod/S-cone photoreceptors in the degenerating STK38L mutant retina.

Authors:  Ágnes I Berta; Kathleen Boesze-Battaglia; Sem Genini; Orly Goldstein; Paul J O'Brien; Ágoston Szél; Gregory M Acland; William A Beltran; Gustavo D Aguirre
Journal:  PLoS One       Date:  2011-09-30       Impact factor: 3.240

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  1 in total

1.  Assembly and Analysis of Unmapped Genome Sequence Reads Reveal Novel Sequence and Variation in Dogs.

Authors:  Lindsay A Holden; Meharji Arumilli; Marjo K Hytönen; Sruthi Hundi; Jarkko Salojärvi; Kim H Brown; Hannes Lohi
Journal:  Sci Rep       Date:  2018-07-18       Impact factor: 4.379

  1 in total

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