The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease.
Ekaterina E Rogaeva,
Yan Y Meng,
Joseph H JH Lee,
Yongjun Y Gu,
Toshitaka T Kawarai,
Fanggeng F Zou,
Taiichi T Katayama,
Clinton T CT Baldwin,
Rong R Cheng,
Hiroshi H Hasegawa,
Fusheng F Chen,
Nobuto N Shibata,
Kathryn L KL Lunetta,
Raphaelle R Pardossi-Piquard,
Christopher C Bohm,
Yosuke Y Wakutani,
L Adrienne LA Cupples,
Karen T KT Cuenco,
Robert C RC Green,
Lorenzo L Pinessi,
Innocenzo I Rainero,
Sandro S Sorbi,
Amalia A Bruni,
Ranjan R Duara,
Robert P RP Friedland,
Rivka R Inzelberg,
Wolfgang W Hampe,
Hideaki H Bujo,
You-Qiang YQ Song,
Olav M OM Andersen,
Thomas E TE Willnow,
Neill N Graff-Radford,
Ronald C RC Petersen,
Dennis D Dickson,
Sandy D SD Der,
Paul E PE Fraser,
Gerold G Schmitt-Ulms,
Steven S Younkin,
Richard R Mayeux,
Lindsay A LA Farrer and
Peter P St George-Hyslop
Nat Genet 39(2):168-77 (2007)
PMID 17220890
PMCID:
PMC2657343
The recycling of the amyloid precursor protein (APP) from the cell surface via the endocytic pathways plays a key role in the generation of amyloid beta peptide (Abeta) in Alzheimer disease. We report here that inherited variants in the SORL1 neuronal sorting receptor are associated with late-onset Alzheimer disease. These variants, which occur in at least two different clusters of intronic sequences within the SORL1 gene (also known as LR11 or SORLA) may regulate tissue-specific expression of SORL1. We also show that SORL1 directs trafficking of APP into recycling pathways and that when SORL1 is underexpressed, APP is sorted into Abeta-generating compartments. These data suggest that inherited or acquired changes in SORL1 expression or function are mechanistically involved in causing Alzheimer disease.
DOI: 10.1038/ng1943
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