Evidence map›Paper›PMID 22768134›Full record

ArticlePloS one2012

Oligonucleotide primers for targeted amplification of single-copy nuclear genes in apocritan Hymenoptera.

Gerrit Hartig, Ralph S Peters, Janus Borner, Claudia Etzbauer, Bernhard Misof, Oliver Niehuis

Abstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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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.

Gerrit HartigZoologisches Forschungsmuseum Alexander Koenig, Zentrum für Molekulare Biodiversitätsforschung, Bonn, Germany.
Ralph S Peters
Janus Borner
Claudia Etzbauer
Bernhard Misof
Oliver Niehuis

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPublished nucleotide sequence data from the mega-diverse insect order Hymenoptera (sawflies, bees, wasps, and ants) are taxonomically scattered and still inadequate for reconstructing a well-supported phylogenetic tree for the order. The analysis of comprehensive multiple gene data sets obtained via targeted PCR could provide a cost-effective solution to this problem. However, oligonucleotide primers for PCR amplification of nuclear genes across a wide range of hymenopteran species are still scarce.

findingsHere we present a suite of degenerate oligonucleotide primer pairs for PCR amplification of 154 single-copy nuclear protein-coding genes from Hymenoptera. These primers were inferred from genome sequence data from nine Hymenoptera (seven species of ants, the honeybee, and the parasitoid wasp Nasonia vitripennis). We empirically tested a randomly chosen subset of these primer pairs for amplifying target genes from six Hymenoptera, representing the families Chrysididae, Crabronidae, Gasteruptiidae, Leucospidae, Pompilidae, and Stephanidae. Based on our results, we estimate that these primers are suitable for studying a large number of nuclear genes across a wide range of apocritan Hymenoptera (i.e., all hymenopterans with a wasp-waist) and of aculeate Hymenoptera in particular (i.e., apocritan wasps with stingers).

conclusionsThe amplified nucleotide sequences are (a) with high probability from single-copy genes, (b) easily generated at low financial costs, especially when compared to phylogenomic approaches, (c) easily sequenced by means of an additionally provided set of sequencing primers, and (d) suitable to address a wide range of phylogenetic questions and to aid rapid species identification via barcoding, as many amplicons contain both exonic and fast-evolving intronic nucleotides.

Indexed as

AnimalsCell NucleusDNA PrimersElectrophoresis, Agar GelGene DosageGenes, InsectHymenopteraMolecular Sequence DataPhylogenyPolymerase Chain ReactionSequence Homology, Nucleic AcidDNA Primers

Identifiers

PMID22768134
PMCPMC3387199

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