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http://purl.uniprot.org/citations/21228389http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21228389http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21228389http://www.w3.org/2000/01/rdf-schema#comment"

Purpose

Olfactomedin 2 (OLFM2) belongs to the family of olfactomedin domain-containing proteins. Genetic data suggest its association with glaucoma in Japanese patients. However, its functions are still elusive. In this study, the properties of mammalian OLFM2 were investigated.

Methods

Expression of the rat and mouse Olfm2 gene was studied by using real-time PCR and in situ hybridization. Substitutions were introduced into OLFM2 by mutagenesis in vitro. Intracellular localization of OLFM2 was studied by confocal microscopy after transient transfection in HEK293 cells. Interaction of OLFM2 with olfactomedin 1 (Olfm1), olfactomedin 3 (Olfm3), myocilin, and gliomedin was studied by using co-immunoprecipitation.

Results

Two major human OLFM2 mRNAs encode secreted proteins with a length of 454 and 478 amino acids. OLFM2 is more closely related to OLFM1 and -3 than to any other family members. Olfm2 showed the most dynamic expression pattern compared with Olfm1 and -3 during mouse eye development and was expressed preferentially in the developing retinal ganglion cell layer. Among three OLFM2 substitutions tested (T86M, R144Q, and L420S), only L420S completely blocked secretion of the protein. OLFM2 interacted with Olfm1 and -3, but not with myocilin and gliomedin. Co-transfection of the L420S mutant with wild-type Olfm1 and -3 significantly inhibited secretion of Olfm1 and -3.

Conclusions

Highly conserved OLFM2 protein may play an important role in the course of retinal and eye development. Severe mutations in one of the closely related olfactomedin domain-containing proteins (Olfm1-3) may block the secretion and probably the activity of all three family members, leading to more pronounced diseases of the retina than the knockout of individual genes."xsd:string
http://purl.uniprot.org/citations/21228389http://purl.org/dc/terms/identifier"doi:10.1167/iovs.10-6356"xsd:string
http://purl.uniprot.org/citations/21228389http://purl.org/dc/terms/identifier"doi:10.1167/iovs.10-6356"xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/author"Sultana A."xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/author"Sultana A."xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/author"Senatorov V.V."xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/author"Senatorov V.V."xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/author"Tomarev S.I."xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/author"Tomarev S.I."xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/author"Nakaya N."xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/author"Nakaya N."xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/name"Invest. Ophthalmol. Vis. Sci."xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/name"Invest. Ophthalmol. Vis. Sci."xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/pages"2584-2592"xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/pages"2584-2592"xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/title"Olfactomedin 2: expression in the eye and interaction with other olfactomedin domain-containing proteins."xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/title"Olfactomedin 2: expression in the eye and interaction with other olfactomedin domain-containing proteins."xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/volume"52"xsd:string
http://purl.uniprot.org/citations/21228389http://purl.uniprot.org/core/volume"52"xsd:string
http://purl.uniprot.org/citations/21228389http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/21228389
http://purl.uniprot.org/citations/21228389http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/21228389