Literature DB >> 11071390

The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition.

S Gerber1, J M Rozet, S I Takezawa, L C dos Santos, L Lopes, O Gribouval, C Penet, I Perrault, D Ducroq, E Souied, M Jeanpierre, S Romana, J Frézal, F Ferraz, R Yu-Umesono, A Munnich, J Kaplan.   

Abstract

The last Crypto-Jews (Marranos) are the survivors of Spanish Jews who were persecuted in the late fifteenth century, escaped to Portugal and were forced to convert to save their lives. Isolated groups still exist in mountainous areas such as Belmonte in the Beira-Baixa province of Portugal. We report here the genetic study of a highly consanguineous endogamic population of Crypto-Jews of Belmonte affected with autosomal recessive retinitis pigmentosa (RP). A genome-wide search for homozygosity allowed us to localize the disease gene to chromosome 15q22-q24 (Zmax=2.95 at theta=0 at the D15S131 locus). Interestingly, the photoreceptor cell-specific nuclear receptor (PNR) gene, the expression of which is restricted to the outer nuclear layer of retinal photoreceptor cells, was found to map to the YAC contig encompassing the disease locus. A search for mutations allowed us to ascribe the RP of Crypto-Jews of Belmonte to a homozygous missense mutation in the PNR gene. Preliminary haplotype studies support the view that this mutation is relatively ancient but probably occurred after the population settled in Belmonte.

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Year:  2000        PMID: 11071390     DOI: 10.1007/s004390000350

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  33 in total

1.  A novel mutation (Cys83Tyr) in the second zinc finger of NR2E3 in enhanced S-cone syndrome.

Authors:  Amândio Rocha-Sousa; Takaaki Hayashi; Nuno Lourenço Gomes; Susana Penas; Elisete Brandão; Paulo Rocha; Mitsuyoshi Urashima; Hisashi Yamada; Hiroshi Tsuneoka; Fernando Falcão-Reis
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2010-08-20       Impact factor: 3.117

2.  Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4.

Authors:  Qingjiong Zhang; Fareeha Zulfiqar; Xueshan Xiao; S Amer Riazuddin; Radha Ayyagari; Farooq Sabar; Raphael Caruso; Paul A Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Journal:  Hum Genet       Date:  2005-09-28       Impact factor: 4.132

3.  An Arg311Gln NR2E3 mutation in a family with classic Goldmann-Favre syndrome.

Authors:  S H Chavala; A Sari; H Lewis; G J T Pauer; E Simpson; S A Hagstrom; E I Traboulsi
Journal:  Br J Ophthalmol       Date:  2005-08       Impact factor: 4.638

4.  A cell cycle-dependent co-repressor mediates photoreceptor cell-specific nuclear receptor function.

Authors:  Shinichiro Takezawa; Atsushi Yokoyama; Maiko Okada; Ryoji Fujiki; Aya Iriyama; Yasuo Yanagi; Hiroaki Ito; Ichiro Takada; Masahiko Kishimoto; Atsushi Miyajima; Ken-Ichi Takeyama; Kazuhiko Umesono; Hirochika Kitagawa; Shigeaki Kato
Journal:  EMBO J       Date:  2007-01-25       Impact factor: 11.598

5.  Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function.

Authors:  Koji M Nishiguchi; James S Friedman; Michael A Sandberg; Anand Swaroop; Eliot L Berson; Thaddeus P Dryja
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-09       Impact factor: 11.205

6.  In pursuit of synthetic modulators for the orphan retina-specific nuclear receptor NR2E3.

Authors:  Qiong Qin; Anna Knapinska; Nicoleta Dobri; Franck Madoux; Peter Chase; Peter Hodder; Konstantin Petrukhin
Journal:  J Ocul Pharmacol Ther       Date:  2012-10-25       Impact factor: 2.671

7.  Echoes from Sepharad: signatures on the maternal gene pool of crypto-Jewish descendants.

Authors:  Inês Nogueiro; João Teixeira; António Amorim; Leonor Gusmão; Luis Alvarez
Journal:  Eur J Hum Genet       Date:  2014-07-30       Impact factor: 4.246

8.  [Multimodal imaging in Goldmann-Favre syndrome].

Authors:  D Valler; M Ulbig; C P Lohmann; M Maier
Journal:  Ophthalmologe       Date:  2018-10       Impact factor: 1.059

9.  New truncation mutation of the NR2E3 gene in a Japanese patient with enhanced S-cone syndrome.

Authors:  Kazuki Kuniyoshi; Takaaki Hayashi; Hiroyuki Sakuramoto; Hiroshi Mishima; Hiroshi Tsuneoka; Kazushige Tsunoda; Takeshi Iwata; Yoshikazu Shimomura
Journal:  Jpn J Ophthalmol       Date:  2016-08-13       Impact factor: 2.447

10.  A comprehensive analysis of sequence variants and putative disease-causing mutations in photoreceptor-specific nuclear receptor NR2E3.

Authors:  Atsuhiro Kanda; Anand Swaroop
Journal:  Mol Vis       Date:  2009-10-24       Impact factor: 2.367

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