Evidence map›Paper›PMID 17376234›Full record

ArticleBMC biology2007

Sequence variation in human succinate dehydrogenase genes: evidence for long-term balancing selection on SDHA.

Bora E Baysal, Elizabeth C Lawrence, Robert E Ferrell

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Biochemical, Molecular, and Clinical Characterization of Succinate Dehydrogenase Subunit A Variants of Unknown Significance.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. GWAS: heritability missing in action?European journal of human genetics : EJHG · 2010
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Adaptive evolution of UGT2B17 copy-number variation.American journal of human genetics · 2008
    Article
  16. Article
  17. Article
  18. Article
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

3 authors at 2 institutions in 1 country.

Bora E BaysalDepartment of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA. baysalb@mwri.magee.edu
Elizabeth C Lawrence
Robert E Ferrell
University of Pittsburgh · USMagee-Womens Research Institute · US

Funding

Epigenetic Regulation of Mitochondiral Complex IIR01CA112364 · NCI · YALE UNIVERSITY · PI SHADEL, GERALD · 2005 to 2010
$997k
NCI NIH HHS CA112364NCI NIH HHS R01 CA112364
6 · The paper itself

Abstract

backgroundBalancing selection operating for long evolutionary periods at a locus is characterized by the maintenance of distinct alleles because of a heterozygote or rare-allele advantage. The loci under balancing selection are distinguished by their unusually high polymorphism levels. In this report, we provide statistical and comparative genetic evidence suggesting that the SDHA gene is under long-term balancing selection. SDHA encodes the major catalytical subunit (flavoprotein, Fp) of the succinate dehydrogenase enzyme complex (SDH; mitochondrial complex II). The inhibition of Fp by homozygous SDHA mutations or by 3-nitropropionic acid poisoning causes central nervous system pathologies. In contrast, heterozygous mutations in SDHB, SDHC, and SDHD, the other SDH subunit genes, cause hereditary paraganglioma (PGL) tumors, which show constitutive activation of pathways induced by oxygen deprivation (hypoxia).

resultsWe sequenced the four SDH subunit genes (10.8 kb) in 24 African American and 24 European American samples. We also sequenced the SDHA gene (2.8 kb) in 18 chimpanzees. Increased nucleotide diversity distinguished the human SDHA gene from its chimpanzee ortholog and from the PGL genes. Sequence analysis uncovered two common SDHA missense variants and refuted the previous suggestions that these variants originate from different genetic loci. Two highly dissimilar SDHA haplotype clusters were present in intermediate frequencies in both racial groups. The SDHA variation pattern showed statistically significant deviations from neutrality by the Tajima, Fu and Li, Hudson-Kreitman-Aguadé, and Depaulis haplotype number tests. Empirically, the elevated values of the nucleotide diversity (% pi = 0.231) and the Tajima statistics (D = 1.954) in the SDHA gene were comparable with the most outstanding cases for balancing selection in the African American population.

conclusionThe SDHA gene has a strong signature of balancing selection. The SDHA variants that have increased in frequency during human evolution might, by influencing the regulation of cellular oxygen homeostasis, confer protection against certain environmental toxins or pathogens that are prevalent in Africa.

Indexed as

Polymorphism, Single NucleotideSelection, GeneticAnimalsBase SequenceElectron Transport Complex IIGene FrequencyHaplotypesHumansMolecular Sequence DataPan troglodytesProtein SubunitsRacial GroupsSequence Homology, Nucleic AcidSuccinate DehydrogenaseTime FactorsElectron Transport Complex IIProtein SubunitsSDHA protein, humanSuccinate Dehydrogenase

Identifiers

PMID17376234
PMCPMC1852088
OpenAlexW2059643938

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.