A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population. Issue 7 (27th November 2015)
- Record Type:
- Journal Article
- Title:
- A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population. Issue 7 (27th November 2015)
- Main Title:
- A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population
- Authors:
- Amy, Maïté
Staehlin, Oliver
René, Frédérique
Blasco, Hélène
Marouillat, Sylviane
Daoud, Hussein
Vourc'h, Patrick
Gordon, Paul H.
Camu, William
Corcia, Philippe
Loeffler, Jean-Philippe
Palkovits, Miklós
Sommer, Wolfgang H.
Andres, Christian R. - Abstract:
- Abstract : Amyotrophic lateral sclerosis is sporadic (SALS) in 90% of cases and has complex environmental and genetic influences. Nogo protein inhibits neurite outgrowth and is overexpressed in muscle in ALS. Our aims were to study the reticulon 4 receptor gene RTN4R which encodes Nogo 1 receptor (NgR1) in SALS, to test if the variants were associated with variable expression of the gene and whether NgR1 protein expression was modified in a transgenic mouse model of ALS. We genotyped three single nucleotide polymorphisms (SNPs; rs701421, rs701427, and rs1567871) of the RTN4R gene in 364 SALS French patients and 430 controls. We examined expression of RTN4R mRNA by quantitative PCR in control post mortem human brain tissue. We determined the expression of NgR1 protein in spinal motor neurons from a SOD1 G86R ALS mouse model. We observed significant associations between SALS and RTN4R alleles. Messenger RNA expression from RTN4R in human cortical brain tissue correlated significantly with the genotypes of rs701427. NgR1 protein expression was reduced in Nogo A positive motor neurons from diseased transgenic animals. In conclusion, these observations suggest that a functional RTN4R gene variant is associated with SALS. This variant may act in concert with other genetic variants or environmental influences.
- Is Part Of:
- Amyotrophic lateral sclerosis and frontotemporal degeneration. Volume 16:Issue 7/8(2015)
- Journal:
- Amyotrophic lateral sclerosis and frontotemporal degeneration
- Issue:
- Volume 16:Issue 7/8(2015)
- Issue Display:
- Volume 16, Issue 7/8 (2015)
- Year:
- 2015
- Volume:
- 16
- Issue:
- 7/8
- Issue Sort Value:
- 2015-0016-NaN-0000
- Page Start:
- 490
- Page End:
- 496
- Publication Date:
- 2015-11-27
- Subjects:
- Nogo-66 receptor -- reticulon 4 receptor gene (RTN4R) -- sporadic amyotrophic lateral sclerosis -- association study -- SNP -- motor neurons -- gene expression
616.839 - Journal URLs:
- http://informahealthcare.com/journal/afd ↗
http://informahealthcare.com ↗ - DOI:
- 10.3109/21678421.2015.1051988 ↗
- Languages:
- English
- ISSNs:
- 2167-8421
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0859.841188
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British Library STI - ELD Digital store - Ingest File:
- 7957.xml