Evidence map›Paper›PMID 12181774›Full record

ArticleAmerican journal of human genetics2002

DNA sequence variation in a 3.7-kb noncoding sequence 5' of the CYP1A2 gene: implications for human population history and natural selection.

S P Wooding, W S Watkins, M J Bamshad, D M Dunn, R B Weiss, L B Jorde

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in American journal of human genetics, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

22 citing papers in PubMed, 91 citations in OpenAlex.

  1. Review
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  9. Caffeine, selected metabolic gene variants, and risk for neural tube defects.Birth defects research. Part A, Clinical and molecular teratology · 2010
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Pharmacogenomics and therapeutic prospects in dementia.European archives of psychiatry and clinical neuroscience · 2008
    Review
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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

6 authors at 1 institution in 1 country.

S P WoodingDepartment of Human Genetics, University of Utah, Salt Lake City, UT, 84112, USA.
W S Watkins
M J Bamshad
D M Dunn
R B Weiss
L B Jorde
University of Utah · US

Funding

VIRAL DAMAGE TO BRAIN AND NEUROMUSCULAR SYSTEMM01RR000064 · NCRR · UNIVERSITY OF UTAH · PI SWOBODA, KATHRYN J. · 1985 to 2008
$21.7M
POPULATION GENETICS OF MOBILE ELEMENTSR01GM059290 · NIGMS · UNIVERSITY OF UTAH · PI BATZER, MARK A, FESCHOTTE, CEDRIC · 1999 to 2018
$8.5M
FULL LENGTH SEQUENCING OF CANCER RELATED CDNASR01ES010058 · NIEHS · UNIVERSITY OF UTAH · PI WEISS, ROBERT B · 1999 to 2001
$2.0M
NCRR NIH HHS M01 RR000064NCRR NIH HHS RR-00064NIEHS NIH HHS ES-10058NIGMS NIH HHS GM-59290NIGMS NIH HHS R01 GM059290
6 · The paper itself

Abstract

CYP1A2 is a cytochrome P450 gene that is involved in human physiological responses to a variety of drugs and toxins. To investigate the role of population history and natural selection in shaping genetic diversity in CYP1A2, we sequenced a 3.7-kb region 5' from CYP1A2 in a diverse collection of 113 individuals from three major continental regions of the Old World (Africa, Asia, and Europe). We also examined sequences in the 90-member National Institutes of Health DNA Polymorphism Discovery Resource (PDR). Eighteen single-nucleotide polymorphisms (SNPs) were found. Most of the high-frequency SNPs found in the Old World sample were also found in the PDR sample. However, six SNPs were detected in the Old World sample but not in the PDR sample, and two SNPs found in the PDR sample were not found in the Old World sample. Most pairs of SNPs were in complete linkage disequilibrium with one another, and there was no indication of a decline of disequilibrium with physical distance in this region. The average +/- SD nucleotide diversity in the Old World sample was 0.00043+/-0.00026. The African population had the highest level of nucleotide diversity and the lowest level of linkage disequilibrium. Two distinct haplotype clusters with broadly overlapping geographical distributions were present. Of the 17 haplotypes found in the Old World sample, 12 were found in the African sample, 8 were found in Indians, 5 were found in non-Indian Asians, and 5 were found in Europeans. Haplotypes found outside Africa were mostly a subset of those found within Africa. These patterns are all consistent with an African origin of modern humans. Seven SNPs were singletons, and the site-frequency spectrum showed a significant departure from neutral expectations, suggesting population expansion and/or natural selection. Comparison with outgroup species showed that four derived SNPs have achieved high (>0.90) frequencies in human populations, a trend consistent with the action of positive natural selection. These patterns have a number of implications for disease-association studies in CYP1A2 and other genes.

Indexed as

Selection, Genetic5' Flanking RegionAfricaAllelesAnimalsAsiaBase SequenceBiological EvolutionCytochrome P-450 CYP1A2EuropeGene FrequencyGenetic VariationHaplotypesHominidaeHumansLinkage DisequilibriumCytochrome P-450 CYP1A2

Identifiers

PMID12181774
PMCPMC379190
OpenAlexW2148896102

What OpenQuestion holds

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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.