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通过等位基因转录的遗传评估鉴定白细胞介素6受体(IL6R)基因中的顺式调控变异。

Identification of cis-regulatory variations in the IL6R gene through the inheritance assessment of allelic transcription.

作者信息

Oh Soo A, Byun Hyejin, Jang Eunsu, Jeong Sangkyun

出版信息

Biochim Biophys Acta. 2014 Jan;1840(1):637-44.

Abstract

BACKGROUND

The level of circulating interleukin-6 receptor in human blood varies depending on the genetic and/or physiological causes, and has been implicated in the development of chronic inflammatory diseases.

METHOD

The cis-regulatory effects of genetic variations on the transcription of interleukin-6 receptor gene, IL6R,were studied by assessing allelic transcriptions in the immortalized lymphocytes derived from unrelated and familial samples.

RESULTS

The assays for allelic transcription in the cells from unrelated subjects demonstrated an extensive and variable range of allelic transcriptional imbalances, suggesting an operation of multiple cis-regulations with varying degrees on the locus. Analysis of the familial samples illustrated the Mendelian inheritance of allelic transcriptions,enabling us to assign each haplotype allele into one of the 3 transcriptional strengths. A comparison of the allele structures based on the transcriptional attributes highlighted 2 SNP variations, rs952146 and rs4845617, as being associated with higher allelic transcription. Consistently, lymphocytes that were homozygous for the 2SNPs exhibited differences in their transcript levels depending on the haplotypes.

CONCLUSION

Inheritance assessment of allelic transcription of IL6R identified 2 SNPs that are associated with transcriptional variation in cis.

GENERAL SIGNIFICANCE

Our results not only demonstrate genetic variations that are associated with IL6R transcription in cis but also demonstrate an effective genetic approach for isolating cis-regulatory variations.

摘要

背景

人血液中循环白细胞介素-6受体水平因遗传和/或生理原因而有所不同,并与慢性炎症性疾病的发生有关。

方法

通过评估来自无关个体和家族样本的永生化淋巴细胞中的等位基因转录,研究基因变异对白介素-6受体基因(IL6R)转录的顺式调节作用。

结果

对无关个体细胞中等位基因转录的检测显示出广泛且可变的等位基因转录失衡范围,表明该基因座存在不同程度的多种顺式调节作用。对家族样本的分析说明了等位基因转录的孟德尔遗传方式,使我们能够将每个单倍型等位基因归为三种转录强度之一。基于转录特性的等位基因结构比较突出了两个单核苷酸多态性(SNP)变异rs952146和rs4845617与较高的等位基因转录有关。同样,这两个SNP的纯合淋巴细胞根据单倍型在转录水平上表现出差异。

结论

对IL6R等位基因转录的遗传评估确定了两个与顺式转录变异相关的SNP。

普遍意义

我们的结果不仅证明了与IL6R顺式转录相关的基因变异,还证明了一种分离顺式调节变异的有效遗传方法。

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