Conceptos Básicos
Transgenerational genetic effects, if they exist at all, are extremely rare in mammals under naturally occurring genetic variation and are unlikely to contribute significantly to phenotypic variance.
Resumen
The study aimed to test the hypothesis of transgenerational genetic effects (TGE) via the paternal lineage in mice. The researchers generated 833 isogenic C57BL/6J (B6) mice that differed only by the presence of one copy of four A/J chromosomes (MMU 15, 17, 19 or X) in the genome of their sire. They measured 25 anatomical traits and performed RNA-Seq on five distinct tissues (heart, liver, pituitary, whole embryo, and placenta) to assess the effect of the non-transmitted paternal A/J chromosomes.
The key findings are:
- There was no evidence of a significant effect from untransmitted A/J sire chromosome alleles, whether on anatomical traits or gene expression level.
- The initial suggestion of differential expression of three genes (Mid1, Crem, and Gm26448) was not replicated in subsequent validation experiments.
- The differential expression of Mid1 in the B6.A-19 consomic-derived isogenic mice was found to be due to a duplication event at the pseudoautosomal region, rather than a TGE.
- The researchers conclude that transgenerational epigenetic memory of non-transmitted paternal alleles, if it exists, is uncommon in mice and likely other mammals.
Estadísticas
There was suggestive evidence (p = 0.0025) for a 6.7% reduction in heart weight in the B6.A-17 N2 consomic-derived line relative to B6.C purebred mice.