TY - JOUR
T1 - Retrotransposons in the Mammalian Male Germline
AU - Zhou, Shumin
AU - Sakashita, Akihiko
AU - Yuan, Shuiqiao
AU - Namekawa, Satoshi H.
N1 - Funding Information:
This study was supported by the National Natural Science Foundation of China (81971444 to S.Y), the Science Technology and Innovation Commission of Shenzhen Municipality (JCYJ20170818160910316 to S.Y.), and National Institute of Health grants (R01GM098605, R01GM122776, R35GM141085 to S.H.N.)..
Publisher Copyright:
© 2023 S. Karger AG. All rights reserved.
PY - 2023/7/1
Y1 - 2023/7/1
N2 - Retrotransposons are a subset of DNA sequences that constitute a large part of the mammalian genome. They can translocate autonomously or non-autonomously, potentially jeopardizing the heritable germline genome. Retrotransposons coevolved with the host genome, and the germline is the prominent battlefield between retrotransposons and the host genome to maximize their mutual fitness. Host genomes have developed various mechanisms to suppress and control retrotransposons, including DNA methylation, histone modifications, and Piwi-interacting RNA (piRNA), for their own benefit. Thus, rapidly evolved retrotransposons often acquire positive functions, including gene regulation within the germline, conferring reproductive fitness in a species over the course of evolution. The male germline serves as an ideal model to examine the regulation and evolution of retrotransposons, resulting in genomic co-evolution with the host genome. In this review, we summarize and discuss the regulatory mechanisms of retrotransposons, stage-by-stage, during male germ cell development, with a particular focus on mice as an extensively studied mammalian model, highlighting suppression mechanisms and emerging functions of retrotransposons in the male germline.
AB - Retrotransposons are a subset of DNA sequences that constitute a large part of the mammalian genome. They can translocate autonomously or non-autonomously, potentially jeopardizing the heritable germline genome. Retrotransposons coevolved with the host genome, and the germline is the prominent battlefield between retrotransposons and the host genome to maximize their mutual fitness. Host genomes have developed various mechanisms to suppress and control retrotransposons, including DNA methylation, histone modifications, and Piwi-interacting RNA (piRNA), for their own benefit. Thus, rapidly evolved retrotransposons often acquire positive functions, including gene regulation within the germline, conferring reproductive fitness in a species over the course of evolution. The male germline serves as an ideal model to examine the regulation and evolution of retrotransposons, resulting in genomic co-evolution with the host genome. In this review, we summarize and discuss the regulatory mechanisms of retrotransposons, stage-by-stage, during male germ cell development, with a particular focus on mice as an extensively studied mammalian model, highlighting suppression mechanisms and emerging functions of retrotransposons in the male germline.
KW - DNA methylation
KW - Histone modifications
KW - Meiosis
KW - Retrotransposons
KW - Spermatogenesis
KW - Transposable elements
KW - piRNA
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U2 - 10.1159/000520683
DO - 10.1159/000520683
M3 - Review article
C2 - 35231923
AN - SCOPUS:85126484544
SN - 1661-5425
VL - 16
SP - 404
EP - 422
JO - Sexual Development
JF - Sexual Development
IS - 5-6
ER -