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Next-generation genotyping of hypervariable loci in many individuals of a non-model species: technical and theoretical implications.
Grogan, Kathleen E; McGinnis, Gwendolyn J; Sauther, Michelle L; Cuozzo, Frank P; Drea, Christine M.
Afiliação
  • Grogan KE; University Program in Ecology, Duke University, Durham, NC, USA. kathleen.e.grogan@gmail.com.
  • McGinnis GJ; Department of Evolutionary Anthropology, Duke University, Durham, NC, USA. kathleen.e.grogan@gmail.com.
  • Sauther ML; Emory University, Room 2006 O. Wayne Rollins Research Center, 1510 Clifton Rd NE, Atlanta, GA, 30322, USA. kathleen.e.grogan@gmail.com.
  • Cuozzo FP; Department of Evolutionary Anthropology, Duke University, Durham, NC, USA.
  • Drea CM; Department of Anthropology, University of Colorado-Boulder, Boulder, CO, USA.
BMC Genomics ; 17: 204, 2016 Mar 08.
Article em En | MEDLINE | ID: mdl-26957424
ABSTRACT

BACKGROUND:

Across species, diversity at the Major Histocompatibility Complex (MHC) is critical to disease resistance and population health; however, use of MHC diversity to quantify the genetic health of populations has been hampered by the extreme variation found in MHC genes. Next generation sequencing (NGS) technology generates sufficient data to genotype even the most diverse species, but workflows for distinguishing artifacts from alleles are still under development. We used NGS to evaluate the MHC diversity of over 300 captive and wild ring-tailed lemurs (Lemur catta Primates Mammalia). We modified a published workflow to address errors that arise from deep sequencing individuals and tested for evidence of selection at the most diverse MHC genes.

RESULTS:

In addition to evaluating the accuracy of 454 Titanium and Ion Torrent PGM for genotyping large populations at hypervariable genes, we suggested modifications to improve current methods of allele calling. Using these modifications, we genotyped 302 out of 319 individuals, obtaining an average sequencing depth of over 1000 reads per amplicon. We identified 55 MHC-DRB alleles, 51 of which were previously undescribed, and provide the first sequences of five additional MHC genes DOA, DOB, DPA, DQA, and DRA. The additional five MHC genes had one or two alleles each with little sequence variation; however, the 55 MHC-DRB alleles showed a high dN/dS ratio and trans-species polymorphism, indicating a history of positive selection. Because each individual possessed 1-7 MHC-DRB alleles, we suggest that ring-tailed lemurs have four, putatively functional, MHC-DRB copies.

CONCLUSIONS:

In the future, accurate genotyping methods for NGS data will be critical to assessing genetic variation in non-model species. We recommend that future NGS studies increase the proportion of replicated samples, both within and across platforms, particularly for hypervariable genes like the MHC. Quantifying MHC diversity within non-model species is the first step to assessing the relationship of genetic diversity at functional loci to individual fitness and population viability. Owing to MHC-DRB diversity and copy number, ring-tailed lemurs may serve as an ideal model for estimating the interaction between genetic diversity, fitness, and environment, especially regarding endangered species.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnicas de Genotipagem / Lemur / Complexo Principal de Histocompatibilidade Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnicas de Genotipagem / Lemur / Complexo Principal de Histocompatibilidade Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article