Abstract

Previous studies have found that fecundity is a multigenic trait regulated, in part, by mitochondrial-nuclear (mit-n) genetic interactions. However, the identification of specific nuclear genetic loci or genes interacting with the mitochondrial genome and contributing to the quantitative trait fecundity is an unsolved issue. Here, a panel of recombinant inbred advanced intercrossed lines (RIAILs), established from a cross between the N2 and CB4856 strains of C. elegans, were used to characterize the underlying genetic basis of mit-n genetic interactions related to fecundity. Sixty-seven single nucleotide polymorphisms (SNPs) were identified by association mapping to be linked with fecundity among 115 SNPs linked to mitotype. This indicated significant epistatic effects between nuclear and mitochondria genetics on fecundity. In addition, two specific nuclear genetic loci interacting with the mitochondrial genome and contributing to fecundity were identified. A significant reduction in fecundity was observed in the RIAILs that carried CB4856 mitochondria and a N2 genotype at locus 1 or a CB4856 genotype at locus 2 relative to the wild-type strains. Then, a hybrid strain (CNC10) was established, which was bred as homoplasmic for the CB4856 mtDNA genome and N2 genotype at locus 1 in the CB4856 nuclear background. The mean fecundity of CNC10 was half the fecundity of the control strain. Several functional characteristics of the mitochondria in CNC10 were also influenced by mit-n interactions. Overall, experimental evidence was presented that specific nuclear genetic loci or genes have interactions with the mitochondrial genome and are associated with fecundity. In total, 18 genes were identified using integrative approaches to have interactions with the mitochondrial genome and to contribute to fecundity.

Highlights

  • Fecundity is a complex trait that determines the potential of a species or population to reproduce

  • Two ‘mito-nuclear’ strains of C. elegans were generated by placing mtDNA from strains of CB4856 onto controlled nuclear backgrounds of N2 (CN30) and by placing mtDNA from strains of N2 onto controlled nuclear backgrounds of CB4856 (NC30) to examine whether a reduction in fecundity was caused by variations in mitochondrial genetics

  • Both hybrid strains (CN30 and NC30) had significantly lower fecundity than the wildtype strains. These results indicated that the reduction in fecundity was mainly caused by the incompatibility of mitochondrial and nuclear single nucleotide polymorphisms (SNPs) in the nematodes

Read more

Summary

Introduction

Fecundity is a complex trait that determines the potential of a species or population to reproduce. There is an accumulation of evidence that suggests a link between mitochondrial genetic variants or mitochondrial dysfunction and fecundity. Mitochondria dysfunction, on the other hand, is known to lead to low sperm quality (Amaral et al, 2013), egg maturation or fertilization abnormalities, embryo loss (Seli, 2016; Tsai and St, 2018) and premature ovarian failure (Pagnamenta et al, 2006). This indicates that multiple elements of mitochondria function/dysfunction influence fecundity

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call