A Human Variant of Glucose-Regulated Protein 94 That Inefficiently Supports IGF Production.
Ontology highlight
ABSTRACT: IGFs are critical for normal intrauterine and childhood growth and sustaining health throughout life. We showed previously that the production of IGF-1 and IGF-2 requires interaction with the chaperone glucose-regulated protein 94 (GRP94) and that the amount of secreted IGFs is proportional to the GRP94 activity. Therefore, we tested the hypothesis that functional polymorphisms of human GRP94 affect IGF production and thereby human health. We describe a hypomorphic variant of human GRP94, P300L, whose heterozygous carriers have 9% lower circulating IGF-1 concentration. P300L was found first in a child with primary IGF deficiency and was later shown to be a noncommon single-nucleotide polymorphism with frequencies of 1%-4% in various populations. When tested in the grp94(-/-) cell-based com
SUBMITTER: Marzec M
PROVIDER: S-EPMC4870884 | biostudies-literature | 2016 May
REPOSITORIES: biostudies-literature
ACCESS DATA