Ramp Sequence May Explain Synonymous Variant Association with Alzheimer's Disease in the Paired Immunoglobulin-like Type 2 Receptor Alpha (PILRA)

斜坡序列可能解释成对免疫球蛋白样 2 型受体 α (PILRA) 中同义变异与阿尔茨海默病的关联

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作者:Justin B Miller ,J Anthony Brandon ,Lauren M Harmon ,Hady W Sabra ,Chloe C Lucido ,Josue D Gonzalez Murcia ,Kayla A Nations ,Samuel H Payne ,Mark T W Ebbert ,John S K Kauwe ,Perry G Ridge

Abstract

Background: The synonymous variant NC_000007.14:g.100373690T>C (rs2405442:T>C) in the Paired Immunoglobulin-like Type 2 Receptor Alpha (PILRA) gene was previously associated with decreased risk for Alzheimer's disease (AD) in genome-wide association studies, but its biological impact is largely unknown. Objective: We hypothesized that rs2405442:T>C decreases mRNA and protein levels by destroying a ramp of slowly translated codons at the 5' end of PILRA. Methods: We assessed rs2405442:T>C predicted effects on PILRA through quantitative polymerase chain reactions (qPCRs) and enzyme-linked immunosorbent assays (ELISAs) using Chinese hamster ovary (CHO) cells. RESULTS: Both mRNA (p = 1.9184 × 10-13) and protein (p = 0.01296) levels significantly decreased in the mutant versus the wildtype in the direction that we predicted based on the destruction of a ramp sequence. Conclusions: We show that rs2405442:T>C alone directly impacts PILRA mRNA and protein expression, and ramp sequences may play a role in regulating AD-associated genes without modifying the protein product. Keywords: Alzheimer’s disease; codon usage bias; disease association; genetic association; ramp sequence.

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