Parental genetic effects on the offspring`s phenotype without direct transmission of the parental gene itself - pathophysiology and clinical evidence.

Fetal Programming Gene Transmission Gene-Environment Interaction Offspring Phenotype Parental Genes

Journal

American journal of physiology. Cell physiology
ISSN: 1522-1563
Titre abrégé: Am J Physiol Cell Physiol
Pays: United States
ID NLM: 100901225

Informations de publication

Date de publication:
16 Jul 2024
Historique:
medline: 16 7 2024
pubmed: 16 7 2024
entrez: 16 7 2024
Statut: aheadofprint

Résumé

Parental genes can influence the phenotype of their offspring through genomic-epigenomic interactions even without the direct inheritance of specific parental genotypes. Maternal genetic variations can affect the ovarian and intrauterine environments and potentially alter lactation behaviors, impacting offspring nutrition and health outcomes independently of the fetal genome. Similarly, paternal genetic changes can affect the endocrine system and vascular functions in the testes, influencing sperm quality and seminal fluid composition. These changes can initiate early epigenetic modifications in sperm, including alterations in microRNAs, tRNA-derived small RNAs, and DNA methylation patterns. These epigenetic modifications might induce further changes in target organs of the offspring, leading to modified gene expression and phenotypic outcomes without transmitting the original parental genetic alterations. This review presents clinical evidence supporting this hypothesis and discusses the potential underlying molecular mechanisms. Parental gene-offspring epigenome-offspring phenotype interactions have been observed in neurocognitive disorders as well as cardio-renal diseases.

Identifiants

pubmed: 39010843
doi: 10.1152/ajpcell.00359.2024
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : China Scholarship Council (CSC)
ID : 202008430176
Organisme : Hunan High-Level Talent Aggregation Project(2022RC4007.
ID : 2022RC4007

Auteurs

Xiaoli Zhang (X)

Nephrology, Heidelberg University, Mannheim, Baden-Würthemberg, Germany.

Berthold Hocher (B)

Nephrology, Heidelberg University, Mannheim, Baden-Würthemberg, Germany.

Classifications MeSH