Imprinted genes and the manipulation of parenting in mammals.
Rosalind M JohnMatthew J HiggsAnthony R IslesPublished in: Nature reviews. Genetics (2023)
Genomic imprinting refers to the parent-of-origin expression of genes, which originates from epigenetic events in the mammalian germ line. The evolution of imprinting may reflect a conflict over resource allocation early in life, with silencing of paternal genes in offspring soliciting increased maternal provision and silencing of maternal genes limiting demands on the mother. Parental caregiving has been identified as an area of potential conflict, with several imprinted genes serendipitously found to directly influence the quality of maternal care. Recent systems biology approaches, based on single-cell RNA sequencing data, support a more deliberate relationship, which is reinforced by the finding that imprinted genes expressed in the offspring influence the quality of maternal caregiving. These bidirectional, reiterative relationships between parents and their offspring are critical both for short-term survival and for lifelong wellbeing, with clear implications for human health.
Keyphrases
- genome wide
- single cell
- human health
- bioinformatics analysis
- genome wide identification
- birth weight
- risk assessment
- healthcare
- high fat diet
- dna methylation
- palliative care
- gene expression
- pregnancy outcomes
- quality improvement
- type diabetes
- genome wide analysis
- high resolution
- rna seq
- climate change
- insulin resistance
- body mass index
- adipose tissue
- physical activity
- metabolic syndrome
- high throughput
- electronic health record
- deep learning
- chronic pain
- gestational age
- transcription factor
- binding protein