Suppr超能文献

在尼古丁成瘾研究中寻找基因关联的基因组功能:ENCODE计划在未来药物基因组学分析中的作用。

Finding genomic function for genetic associations in nicotine addiction research: the ENCODE project's role in future pharmacogenomic analysis.

作者信息

Vandenbergh David J, Schlomer Gabriel L

机构信息

Department of Biobehavioral Health, The Pennsylvania State University, 219 Biobehavioral Health Building, University Park, PA 16802, USA; Penn State Institute of the Neurosciences, 101 Life Sciences Building, University Park, PA 16802, USA.

Department of Human Development and Family Studies, The Pennsylvania State University, 315 Health and Human Development, East, University Park, PA 16802, USA.

出版信息

Pharmacol Biochem Behav. 2014 Aug;123:34-44. doi: 10.1016/j.pbb.2014.01.009. Epub 2014 Jan 31.

Abstract

Tobacco-related behaviors and the underlying addiction to nicotine are complex tangles of genetic and environmental factors. Efforts to understand the genetic component of these traits have identified sites in the genome (single nucleotide polymorphisms, or SNPs) that might account for some part of the role of genetics in nicotine addiction. Encouragingly, some of these candidate SNPs remain significant in meta-analyses. However, genetic associations cannot be fully assessed, regardless of statistical significance, without an understanding of the functional consequences of the alleles present at these SNPs. The proper experimental test for allelic function can be very difficult to define, representing a roadblock in translating genetic results into treatment to prevent smoking and other nicotine-related behaviors. This roadblock can be navigated in part with a new web-based tool, the Encyclopedia of DNA Elements (ENCODE). ENCODE is a compilation of searchable data on several types of biochemical functions or "marks" across the genome. These data can be queried for the co-localization of a candidate SNP and a biochemical mark. The presence of a SNP within a marked region of DNA enables the generation of better-informed hypotheses to test possible functional roles of alleles at a candidate SNP. Two examples of such co-localizations are presented. One example reveals ENCODE's ability to relate a candidate SNP's function with a gene very far from the physical location of the SNP. The second example reveals a new potential function of the SNP, rs4105144, that has been genetically associated with the number of cigarettes smoked per day. Details for accessing the ENCODE data for this SNP are provided to serve as a tutorial. By serving as a bridge between genetic associations and biochemical function, ENCODE has the power to propel progress in untangling the genetic aspects of nicotine addiction - a major public health concern.

摘要

与烟草相关的行为以及对尼古丁的潜在成瘾是遗传和环境因素的复杂交织。了解这些特征的遗传成分的努力已经在基因组中确定了一些位点(单核苷酸多态性,即SNPs),这些位点可能在尼古丁成瘾的遗传作用中占一定比例。令人鼓舞的是,其中一些候选SNPs在荟萃分析中仍然具有显著性。然而,如果不了解这些SNPs处存在的等位基因的功能后果,无论统计显著性如何,遗传关联都无法得到充分评估。确定等位基因功能的适当实验测试可能非常难以定义,这是将遗传结果转化为预防吸烟和其他与尼古丁相关行为的治疗方法的一个障碍。可以通过一种新的基于网络的工具——DNA元件百科全书(ENCODE)在一定程度上克服这个障碍。ENCODE是关于全基因组几种生化功能或“标记”的可搜索数据的汇编。可以查询这些数据以了解候选SNP与生化标记的共定位情况。DNA标记区域内SNP的存在能够产生更有依据的假设,以测试候选SNP处等位基因可能的功能作用。本文给出了两个这样的共定位例子。一个例子揭示了ENCODE将候选SNP的功能与距离该SNP物理位置很远的一个基因联系起来的能力。第二个例子揭示了SNP rs4105144的一种新的潜在功能,该SNP在遗传上与每天吸烟的数量相关。文中提供了访问该SNP的ENCODE数据的详细信息作为教程。通过在遗传关联和生化功能之间架起一座桥梁,ENCODE有能力推动在解开尼古丁成瘾的遗传方面取得进展,而尼古丁成瘾是一个主要的公共卫生问题。

相似文献

2
4
Tobacco addiction and pharmacogenetics of nicotine metabolism.
J Neurogenet. 2009;23(3):262-71. doi: 10.1080/01677060802572903. Epub 2009 Jan 19.
5
Associations of nicotine intake measures with CHRN genes in Finnish smokers.
Nicotine Tob Res. 2011 Aug;13(8):686-90. doi: 10.1093/ntr/ntr059. Epub 2011 Apr 16.
7
Genome-Wide Association of the Laboratory-Based Nicotine Metabolite Ratio in Three Ancestries.
Nicotine Tob Res. 2016 Sep;18(9):1837-1844. doi: 10.1093/ntr/ntw117. Epub 2016 Apr 25.
8
Association of a variant in the muscarinic acetylcholine receptor 2 gene (CHRM2) with nicotine addiction.
Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):684-690. doi: 10.1002/ajmg.b.31011.

引用本文的文献

1
A 5-Factor Framework for Assessing Tobacco Use Disorder.
Tob Use Insights. 2021 Feb 26;14:1179173X21998355. doi: 10.1177/1179173X21998355. eCollection 2021.
2
Translating the Habenula-From Rodents to Humans.
Biol Psychiatry. 2017 Feb 15;81(4):296-305. doi: 10.1016/j.biopsych.2016.06.003. Epub 2016 Jun 7.
4
An Adolescent Substance Prevention Model Blocks the Effect of CHRNA5 Genotype on Smoking During High School.
Nicotine Tob Res. 2016 Feb;18(2):212-20. doi: 10.1093/ntr/ntv095. Epub 2015 May 4.
5
Contribution of Variants in CHRNA5/A3/B4 Gene Cluster on Chromosome 15 to Tobacco Smoking: From Genetic Association to Mechanism.
Mol Neurobiol. 2016 Jan;53(1):472-484. doi: 10.1007/s12035-014-8997-x. Epub 2014 Dec 5.
6
Gene-environment interaction research in psychiatric epidemiology: a framework and implications for study design.
Soc Psychiatry Psychiatr Epidemiol. 2014 Oct;49(10):1525-9. doi: 10.1007/s00127-014-0954-5. Epub 2014 Sep 13.

本文引用的文献

1
Next Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data.
Annu Rev Stat Appl. 2014 Jan 1;1(1):279-300. doi: 10.1146/annurev-statistics-022513-115638.
2
Cis-regulatory variants affect CHRNA5 mRNA expression in populations of African and European ancestry.
PLoS One. 2013 Nov 26;8(11):e80204. doi: 10.1371/journal.pone.0080204. eCollection 2013.
3
Impact of nicotine metabolism on nicotine's pharmacological effects and behavioral responses: insights from a Cyp2a(4/5)bgs-null mouse.
J Pharmacol Exp Ther. 2013 Dec;347(3):746-54. doi: 10.1124/jpet.113.208256. Epub 2013 Sep 17.
4
Functional characterization of SNPs in CHRNA3/B4 intergenic region associated with drug behaviors.
Brain Res. 2013 Sep 5;1529:1-15. doi: 10.1016/j.brainres.2013.07.017. Epub 2013 Jul 18.
5
Meta-analysis methods for genome-wide association studies and beyond.
Nat Rev Genet. 2013 Jun;14(6):379-89. doi: 10.1038/nrg3472. Epub 2013 May 9.
6
The ENCODE project: missteps overshadowing a success.
Curr Biol. 2013 Apr 8;23(7):R259-61. doi: 10.1016/j.cub.2013.03.023.
7
Unraveling the neurobiology of nicotine dependence using genetically engineered mice.
Curr Opin Neurobiol. 2013 Aug;23(4):493-9. doi: 10.1016/j.conb.2013.02.013. Epub 2013 Mar 29.
9
Is junk DNA bunk? A critique of ENCODE.
Proc Natl Acad Sci U S A. 2013 Apr 2;110(14):5294-300. doi: 10.1073/pnas.1221376110. Epub 2013 Mar 11.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验