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与α2-HS糖蛋白(胎球蛋白-A)多态性相关的mRNA等位基因失衡

Allelic Imbalance of mRNA Associated with α2-HS Glycoprotein (Fetuin-A) Polymorphism.

作者信息

Inaoka Yoshihiko, Osawa Motoki, Mukasa Nahoko, Miyashita Keiko, Satoh Fumiko, Kakimoto Yu

机构信息

Department of Forensic Medicine, Tokai University School of Medicine, Isehara, Kanagawa 259-1193, Japan.

出版信息

Dis Markers. 2015;2015:865053. doi: 10.1155/2015/865053. Epub 2015 Oct 15.

Abstract

Alpha 2-HS glycoprotein (AHSG), also designated as fetuin-A, exhibits polymorphism in population genetics consisting of two major alleles of AHSG(∗) 1 and AHSG(∗) 2. The serum level in the AHSG(∗) 1 homozygote is significantly higher than that of the AHSG(∗) 2 homozygote. This study examined the molecular mechanism for the cis-regulatory expression. To quantitate allele-specific mRNA in intra-assays of the heterozygote, RT-PCR method employing primers that were incorporated to the two closely located SNPs was developed. The respective magnitudes of AHSG(∗) 1 to AHSG(∗) 2 in the liver tissues and hepatic culture cells of PLC/PRF/5 were determined quantitatively as 2.5-fold and 6.2-fold. The mRNA expressional difference of two major alleles was observed, which is consistent with that in the serum level. The culture cells carried heterozygous genotypes in rs4917 and rs4918, but homozygous one in rs2248690. It was unlikely that the imbalance was derived from the SNP located in the promotor site. Furthermore, to investigate the effect of mRNA degradation, RNA synthesis in the cell culture was inhibited potently by the addition of actinomycin-D. No marked change was apparent between the two alleles. The results indicated that the cis-regulatory expressional difference is expected to occur at the level of transcription or splicing of mRNA.

摘要

α2-HS糖蛋白(AHSG),也被称为胎球蛋白-A,在群体遗传学中表现出多态性,由AHSG(∗)1和AHSG(∗)2两个主要等位基因组成。AHSG(∗)1纯合子的血清水平显著高于AHSG(∗)2纯合子。本研究探讨了顺式调控表达的分子机制。为了在杂合子的实验中定量等位基因特异性mRNA,开发了一种使用与两个紧密相邻的单核苷酸多态性(SNP)结合的引物的逆转录聚合酶链反应(RT-PCR)方法。在PLC/PRF/5的肝组织和肝培养细胞中,AHSG(∗)1与AHSG(∗)2的各自含量经定量测定分别为2.5倍和6.2倍。观察到两个主要等位基因的mRNA表达差异,这与血清水平的差异一致。培养细胞在rs4917和rs4918位点携带杂合基因型,但在rs2248690位点携带纯合基因型。这种失衡不太可能源于启动子位点的SNP。此外,为了研究mRNA降解的影响,通过添加放线菌素-D有效地抑制了细胞培养中的RNA合成。两个等位基因之间没有明显变化。结果表明,顺式调控表达差异预计发生在mRNA转录或剪接水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a925/4624919/229f6b7ae290/DM2015-865053.001.jpg

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