학술논문

Endogenous retroviruses drive species-specific germline transcriptomes in mammals
Document Type
article
Source
Nature Structural & Molecular Biology. 27(10)
Subject
Biological Sciences
Biomedical and Clinical Sciences
Genetics
Contraception/Reproduction
1.1 Normal biological development and functioning
Underpinning research
Animals
Chromatin
Endogenous Retroviruses
Enhancer Elements
Genetic
Gene Expression Regulation
Viral
Humans
Long Interspersed Nucleotide Elements
Male
Mammals
Meiosis
Mice
Inbred C57BL
Mice
Transgenic
Mitosis
Mutation
Proto-Oncogene Proteins c-myb
Repetitive Sequences
Nucleic Acid
Rodentia
Spermatogenesis
Spermatozoa
Trans-Activators
Transcriptome
Chemical Sciences
Medical and Health Sciences
Biophysics
Developmental Biology
Biological sciences
Biomedical and clinical sciences
Chemical sciences
Language
Abstract
Gene regulation in the germline ensures the production of high-quality gametes, long-term maintenance of the species and speciation. Male germline transcriptomes undergo dynamic changes after the mitosis-to-meiosis transition and have been subject to evolutionary divergence among mammals. However, the mechanisms underlying germline regulatory divergence remain undetermined. Here, we show that endogenous retroviruses (ERVs) influence species-specific germline transcriptomes. After the mitosis-to-meiosis transition in male mice, specific ERVs function as active enhancers to drive germline genes, including a mouse-specific gene set, and bear binding motifs for critical regulators of spermatogenesis, such as A-MYB. This raises the possibility that a genome-wide transposition of ERVs rewired germline gene expression in a species-specific manner. Of note, independently evolved ERVs are associated with the expression of human-specific germline genes, demonstrating the prevalence of ERV-driven mechanisms in mammals. Together, we propose that ERVs fine-tune species-specific transcriptomes in the mammalian germline.