Evidence map›Paper›PMID 42055329›Full record

ArticleThe Journal of biological chemistry2026

A functional SNP rs12718466 in APOA1 promoter modulates gene expression via interaction with SOX7.

Yuichi Aita, Yoshinori Takeuchi, Yukari Masuda, Zahra Mehrazad Saber, Samia Karkoutly, Duhan Tao, Chen Ye, Tsolmon Mendsaikhan, Rika Saikawa, Yasuyuki Kondo and 6 more

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Yuichi AitaDivision of Endocrinology and Metabolism, Department of Medicine, Jichi Medical University, Tochigi, Japan; Nutrigenomics Research Group, Institute of Medicine, University of Tsukuba, Ibaraki, Japan.
Yoshinori TakeuchiDivision of Endocrinology and Metabolism, Department of Medicine, Jichi Medical University, Tochigi, Japan.
Yukari MasudaDivision of Endocrinology and Metabolism, Department of Medicine, Jichi Medical University, Tochigi, Japan.
Zahra Mehrazad SaberDivision of Endocrinology and Metabolism, Department of Medicine, Jichi Medical University, Tochigi, Japan.
Samia KarkoutlyDivision of Endocrinology and Metabolism, Department of Medicine, Jichi Medical University, Tochigi, Japan.
Duhan TaoDivision of Endocrinology and Metabolism, Department of Medicine, Jichi Medical University, Tochigi, Japan; Nutrigenomics Research Group, Institute of Medicine, University of Tsukuba, Ibaraki, Japan.
Chen YeDivision of Endocrinology and Metabolism, Department of Medicine, Jichi Medical University, Tochigi, Japan; Nutrigenomics Research Group, Institute of Medicine, University of Tsukuba, Ibaraki, Japan.
Tsolmon MendsaikhanDivision of Endocrinology and Metabolism, Department of Medicine, Jichi Medical University, Tochigi, Japan.
Rika SaikawaDivision of Endocrinology and Metabolism, Department of Medicine, Jichi Medical University, Tochigi, Japan.
Yasuyuki KondoDivision of Endocrinology and Metabolism, Department of Medicine, Jichi Medical University, Tochigi, Japan.
Yuki MurayamaNutrigenomics Research Group, Institute of Medicine, University of Tsukuba, Ibaraki, Japan; Department of Internal Medicine (Endocrinology and Metabolism), Institute of Medicine, University of Tsukuba, Ibaraki, Japan.
Akito ShikamaNutrigenomics Research Group, Institute of Medicine, University of Tsukuba, Ibaraki, Japan; Department of Internal Medicine (Endocrinology and Metabolism), Institute of Medicine, University of Tsukuba, Ibaraki, Japan.
Takashi MatsuzakaDepartment of Internal Medicine (Endocrinology and Metabolism), Institute of Medicine, University of Tsukuba, Ibaraki, Japan.
Hitoshi ShimanoDepartment of Internal Medicine (Endocrinology and Metabolism), Institute of Medicine, University of Tsukuba, Ibaraki, Japan.
Yasushi KawakamiDepartment of Internal Medicine (Endocrinology and Metabolism), Institute of Medicine, University of Tsukuba, Ibaraki, Japan.
Naoya YahagiDivision of Endocrinology and Metabolism, Department of Medicine, Jichi Medical University, Tochigi, Japan; Nutrigenomics Research Group, Institute of Medicine, University of Tsukuba, Ibaraki, Japan; Department of Internal Medicine (Endocrinology and Metabolism), Institute of Medicine, University of Tsukuba, Ibaraki, Japan. Electronic address: nyahagi-tky@umin.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasma concentration of high-density lipoprotein cholesterol (HDL-C) is among the most important risk factors for coronary artery disease and apolipoprotein A1 (APOA1) is an essential apolipoprotein that constitutes HDL. However, few comprehensive searches have been conducted to identify noncoding functional SNPs around the APOA1 gene. In this study, we report the identification of a functional SNP, rs12718466, which influences hepatocyte-specific APOA1 gene expression. Furthermore, we identified SRY-box transcription factor 7 (SOX7) as the transcription factor interacting with the rs12718466 SNP, using a novel screening method Transcription Factor Expression Library scan, which employs a comprehensive library of mouse transcription factors. SOX7 binding is allele-dependent, with stronger binding to the normal allele leading to increased APOA1 transcription. In vitro experiments in hepatocytes and in vivo experiments in mice confirmed that overexpressing SOX7 increased APOA1 expression, while knocking it down decreased both APOA1 gene expression and plasma HDL-C levels. Our research demonstrates that rs12718466 is a functional SNP that modulates APOA1 gene expression through its interaction with SOX7, thereby affecting plasma HDL-C concentrations.

Indexed as

Apolipoprotein A-IPolymorphism, Single NucleotidePromoter Regions, GeneticSOXF Transcription FactorsAnimalsCell LineCholesterol, HDLGene Expression RegulationHepatocytesHumansMiceProtein BindingAPOA1 protein, humanApolipoprotein A-ICholesterol, HDLSOX7 protein, humanSOXF Transcription Factorsfunctional SNPhigh-density lipoprotein cholesteroltranscription factor

Identifiers

PMID42055329
PMCPMC13226946

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.