Evidence map›Paper›PMID 27188709›Full record

ArticleBMC genetics2016

The relationship between mitochondrial DNA haplotype and the reproductive capacity of domestic pigs (Sus scrofa domesticus).

Te-Sha Tsai, Sriram Rajasekar, Justin C St John

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Article in BMC genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

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0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

  1. Review
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  7. The role of mtDNA in oocyte quality and embryo development.Molecular reproduction and development · 2023
    Review
  8. Article
  9. Article
  10. Observational
  11. Mitochondrial DNA Diversity in Large White Pigs in Russia.Animals : an open access journal from MDPI · 2020
    Article
  12. Article
  13. Article
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  16. Article
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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Te-Sha TsaiCentre for Genetic Diseases, Hudson Institute of Medical Research, 27-31 Wright Street, Clayton, Vic, 3168, Australia.
Sriram RajasekarCentre for Genetic Diseases, Hudson Institute of Medical Research, 27-31 Wright Street, Clayton, Vic, 3168, Australia.
Justin C St JohnCentre for Genetic Diseases, Hudson Institute of Medical Research, 27-31 Wright Street, Clayton, Vic, 3168, Australia. justin.stjohn@hudson.org.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe maternally inherited mitochondrial genome encodes key proteins of the electron transfer chain, which produces the vast majority of cellular ATP. Mitochondrial DNA (mtDNA) present in the mature oocyte acts as a template for all mtDNA that is replicated during development to meet the specific energy requirements of each tissue. Individuals that share a maternal lineage cluster into groupings known as mtDNA haplotypes. MtDNA haplotypes confer advantages and disadvantages to an organism and this affects its phenotype. In livestock, certain mtDNA haplotypes are associated with improved milk and meat quality, whilst, other species, mtDNA haplotypes have shown increased longevity, growth and susceptibility to diseases. In this work, we have set out to determine whether mtDNA haplotypes influence reproductive capacity. This has been undertaken using a pig model.

resultsTo determine the genetic diversity of domestic pigs in Australia, we have sequenced the D-loop region of 368 pigs, and identified five mtDNA haplotypes (A to E). To assess reproductive capacity, we compared oocyte maturation, fertilization and development to blastocyst, and found that there were significant differences for maturation and fertilization amongst the haplotypes. We then determined that haplotypes C, D and E produced significantly larger litters. When we assessed the conversion of developmentally competent oocytes and their subsequent developmental stages to offspring, we found that haplotypes A and B had the lowest reproductive efficiencies. Amongst the mtDNA haplotypes, the number of mtDNA variants harbored at >25 % correlated with oocyte quality. MtDNA copy number for developmentally competent oocytes positively correlated with the level of the 16383delC variant. This variant is located in the conserved sequence box II, which is a regulatory region for mtDNA transcription and replication.

conclusionsWe have identified five mtDNA haplotypes in Australian domestic pigs indicating that genetic diversity is restricted. We have also shown that there are differences in reproductive capacity amongst the mtDNA haplotypes. We conclude that mtDNA haplotypes affect pig reproductive capacity and can be used as a marker to complement current selection methods to identify productive pigs.

Indexed as

HaplotypesAnimalsDNA, MitochondrialEmbryonic DevelopmentFemaleLitter SizeOocytesReproductionSus scrofaDNA, Mitochondrial

Identifiers

PMID27188709
PMCPMC4870755

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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.