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Isolated and syndromic retinal dystrophy caused by biallelic mutations in RCBTB1, a gene implicated in ubiquitination

Frauke Coppieters UGent, Giulia Ascari UGent, Katharina Dannhausen, Konstantinos Nikopoulos, Frank Peelman UGent, Marcus Karlstetter, Mingchu Xu, Cécile Brachet, Isabelle Meunier, Miltiadis K Tsilimbaris, et al. (2016) AMERICAN JOURNAL OF HUMAN GENETICS. 99(2). p.470-480
abstract
Inherited retinal dystrophies (iRDs) are a group of genetically and clinically heterogeneous conditions resulting from mutations in over 250 genes. Here, homozygosity mapping and whole-exome sequencing (WES) in a consanguineous family revealed a homozygous missense mutation, c.973C>T (p.His325Tyr), in RCBTB1. In affected individuals, it was found to segregate with retinitis pigmentosa (RP), goiter, primary ovarian insufficiency, and mild intellectual disability. Subsequent analysis of WES data in different cohorts uncovered four additional homozygous missense mutations in five unrelated families in whom iRD segregates with or without syndromic features. Ocular phenotypes ranged from typical RP starting in the second decade to chorioretinal dystrophy with a later age of onset. The five missense mutations affect highly conserved residues either in the sixth repeat of the RCC1 domain or in the BTB1 domain. A founder haplotype was identified for mutation c.919G>A (p.Val307Met), occurring in two families of Mediterranean origin. We showed ubiquitous mRNA expression of RCBTB1 and demonstrated predominant RCBTB1 localization in human inner retina. RCBTB1 was very recently shown to be involved in ubiquitination, more specifically as a CUL3 substrate adaptor. Therefore, the effect on different components of the CUL3 and NFE2L2 (NRF2) pathway was assessed in affected individuals' lymphocytes, revealing decreased mRNA expression of NFE2L2 and several NFE2L2 target genes. In conclusion, our study puts forward mutations in RCBTB1 as a cause of autosomal-recessive non-syndromic and syndromic iRD. Finally, our data support a role for impaired ubiquitination in the pathogenetic mechanism of RCBTB1 mutations.
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
DOMINANT RETINITIS-PIGMENTOSA, TRANSCRIPTION FACTOR NRF2, CHRONIC LYMPHOCYTIC-LEUKEMIA, CONJUGATING ENZYME, PROTEASOME SYSTEM, EXPRESSION ANALYSIS, CHROMOSOME 13Q14, EPITHELIAL-CELLS, RESPONSE ELEMENT, PROTEIN
journal title
AMERICAN JOURNAL OF HUMAN GENETICS
Am. J. Hum. Genet.
volume
99
issue
2
pages
470 - 480
Web of Science type
Article
Web of Science id
000381617200019
JCR category
GENETICS & HEREDITY
JCR impact factor
9.025 (2016)
JCR rank
8/166 (2016)
JCR quartile
1 (2016)
ISSN
0002-9297
DOI
10.1016/j.ajhg.2016.06.017
language
English
UGent publication?
yes
classification
A1
additional info
the first two authors contributed equally to this work
copyright statement
Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
id
8501351
handle
http://hdl.handle.net/1854/LU-8501351
date created
2017-01-10 21:29:40
date last changed
2017-04-13 13:15:01
@article{8501351,
  abstract     = {Inherited retinal dystrophies (iRDs) are a group of genetically and clinically heterogeneous conditions resulting from mutations in over 250 genes. Here, homozygosity mapping and whole-exome sequencing (WES) in a consanguineous family revealed a homozygous missense mutation, c.973C{\textrangle}T (p.His325Tyr), in RCBTB1. In affected individuals, it was found to segregate with retinitis pigmentosa (RP), goiter, primary ovarian insufficiency, and mild intellectual disability. Subsequent analysis of WES data in different cohorts uncovered four additional homozygous missense mutations in five unrelated families in whom iRD segregates with or without syndromic features. Ocular phenotypes ranged from typical RP starting in the second decade to chorioretinal dystrophy with a later age of onset. The five missense mutations affect highly conserved residues either in the sixth repeat of the RCC1 domain or in the BTB1 domain. A founder haplotype was identified for mutation c.919G{\textrangle}A (p.Val307Met), occurring in two families of Mediterranean origin. We showed ubiquitous mRNA expression of RCBTB1 and demonstrated predominant RCBTB1 localization in human inner retina. RCBTB1 was very recently shown to be involved in ubiquitination, more specifically as a CUL3 substrate adaptor. Therefore, the effect on different components of the CUL3 and NFE2L2 (NRF2) pathway was assessed in affected individuals' lymphocytes, revealing decreased mRNA expression of NFE2L2 and several NFE2L2 target genes. In conclusion, our study puts forward mutations in RCBTB1 as a cause of autosomal-recessive non-syndromic and syndromic iRD. Finally, our data support a role for impaired ubiquitination in the pathogenetic mechanism of RCBTB1 mutations.},
  author       = {Coppieters, Frauke and Ascari, Giulia and Dannhausen, Katharina and Nikopoulos, Konstantinos and Peelman, Frank and Karlstetter, Marcus and Xu, Mingchu and Brachet, C{\'e}cile and Meunier, Isabelle and Tsilimbaris, Miltiadis~K and Tsika, Chrysanthi and Blazaki, Styliani~V and Vergult, Sarah and Farinelli, Pietro and Van Laethem, Thalia and Bauwens, Miriam and DE BRUYNE, MARIEKE and Chen, Rui and Langmann, Thomas and Sui, Ruifang and Meire, Fran\c{c}oise and Rivolta, Carlo and Hamel, Christian~P and Leroy, Bart and De Baere, Elfride},
  issn         = {0002-9297},
  journal      = {AMERICAN JOURNAL OF HUMAN GENETICS},
  keyword      = {DOMINANT RETINITIS-PIGMENTOSA,TRANSCRIPTION FACTOR NRF2,CHRONIC LYMPHOCYTIC-LEUKEMIA,CONJUGATING ENZYME,PROTEASOME SYSTEM,EXPRESSION ANALYSIS,CHROMOSOME 13Q14,EPITHELIAL-CELLS,RESPONSE ELEMENT,PROTEIN},
  language     = {eng},
  number       = {2},
  pages        = {470--480},
  title        = {Isolated and syndromic retinal dystrophy caused by biallelic mutations in RCBTB1, a gene implicated in ubiquitination},
  url          = {http://dx.doi.org/10.1016/j.ajhg.2016.06.017},
  volume       = {99},
  year         = {2016},
}

Chicago
Coppieters, Frauke, Giulia Ascari, Katharina Dannhausen, Konstantinos Nikopoulos, Frank Peelman, Marcus Karlstetter, Mingchu Xu, et al. 2016. “Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in Ubiquitination.” American Journal of Human Genetics 99 (2): 470–480.
APA
Coppieters, F., Ascari, G., Dannhausen, K., Nikopoulos, K., Peelman, F., Karlstetter, M., Xu, M., et al. (2016). Isolated and syndromic retinal dystrophy caused by biallelic mutations in RCBTB1, a gene implicated in ubiquitination. AMERICAN JOURNAL OF HUMAN GENETICS, 99(2), 470–480.
Vancouver
1.
Coppieters F, Ascari G, Dannhausen K, Nikopoulos K, Peelman F, Karlstetter M, et al. Isolated and syndromic retinal dystrophy caused by biallelic mutations in RCBTB1, a gene implicated in ubiquitination. AMERICAN JOURNAL OF HUMAN GENETICS. 2016;99(2):470–80.
MLA
Coppieters, Frauke, Giulia Ascari, Katharina Dannhausen, et al. “Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in Ubiquitination.” AMERICAN JOURNAL OF HUMAN GENETICS 99.2 (2016): 470–480. Print.