Evidence map›Paper›PMID 33256598›Full record

ArticleBMC genomics2020

Highly diversified core promoters in the human genome and their effects on gene expression and disease predisposition.

Hemant Gupta, Khyati Chandratre, Siddharth Sinha, Teng Huang, Xiaobing Wu, Jian Cui, Michael Q Zhang, San Ming Wang

Open access · goldAbstract read
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Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 39% of its field
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

4 citing papers in PubMed, 6 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Hemant GuptaCancer Centre and Institute of Translational Medicine, Faculty of Health Sciences, University of Macau, Macau, SAR, China.
Khyati ChandratreCancer Centre and Institute of Translational Medicine, Faculty of Health Sciences, University of Macau, Macau, SAR, China.
Siddharth SinhaCancer Centre and Institute of Translational Medicine, Faculty of Health Sciences, University of Macau, Macau, SAR, China.
Teng HuangCancer Centre and Institute of Translational Medicine, Faculty of Health Sciences, University of Macau, Macau, SAR, China.
Xiaobing WuCancer Centre and Institute of Translational Medicine, Faculty of Health Sciences, University of Macau, Macau, SAR, China.
Jian CuiEppley Institute for Cancer Research, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Michael Q ZhangDepartment of Biological Sciences, Center for Systems Biology, University of Texas at Dallas, Richardson, TX, 75080, USA.
San Ming WangCancer Centre and Institute of Translational Medicine, Faculty of Health Sciences, University of Macau, Macau, SAR, China. sanmingwang@um.edu.mo.ORCID http://orcid.org/0000-0002-2172-1320
University of Macau · MOThe University of Texas at Dallas · USUniversity of Nebraska Medical Center · US

Funding

Faculty of Health Sciences, University of Macau FHSIG/SW/0007/2020PMacau Science and Technology Development Fund 085/2017/A2Ministry of Science and Technology of the People's Republic of China 0077/2019/ AMJUniversidade de Macau MYRG2019-00018-FHSUniversidade de Macau (MO) SRG2017-00097-FHS
6 · The paper itself

Abstract

backgroundCore promoter controls transcription initiation. However, little is known for core promoter diversity in the human genome and its relationship with diseases. We hypothesized that as a functional important component in the genome, the core promoter in the human genome could be under evolutionary selection, as reflected by its highly diversification in order to adjust gene expression for better adaptation to the different environment.

resultsApplying the "Exome-based Variant Detection in Core-promoters" method, we analyzed human core-promoter diversity by using the 2682 exome data sets of 25 worldwide human populations sequenced by the 1000 Genome Project. Collectively, we identified 31,996 variants in the core promoter region (- 100 to + 100) of 12,509 human genes ( https://dbhcpd.fhs.um.edu.mo ). Analyzing the rich variation data identified highly ethnic-specific patterns of core promoter variation between different ethnic populations, the genes with highly variable core promoters, the motifs affected by the variants, and their involved functional pathways. eQTL test revealed that 12% of core promoter variants can significantly alter gene expression level. Comparison with GWAS data we located 163 variants as the GWAS identified traits associated with multiple diseases, half of these variants can alter gene expression.

conclusionData from our study reals the highly diversified nature of core promoter in the human genome, and highlights that core promoter variation could play important roles not only in gene expression regulation but also in disease predisposition.

Indexed as

Gene Expression RegulationGenome, HumanBiological EvolutionGene ExpressionHumansPromoter Regions, Genetic1000 genomesCore promotereQTLExomeGWASVariation

Identifiers

PMID33256598
PMCPMC7706239
OpenAlexW3108920433

What OpenQuestion holds

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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.