TY - JOUR
T1 - Meiosis-specific ZFP541 repressor complex promotes developmental progression of meiotic prophase towards completion during mouse spermatogenesis
AU - Horisawa-Takada, Yuki
AU - Kodera, Chisato
AU - Takemoto, Kazumasa
AU - Sakashita, Akihiko
AU - Horisawa, Kenichi
AU - Maeda, Ryo
AU - Shimada, Ryuki
AU - Usuki, Shingo
AU - Fujimura, Sayoko
AU - Tani, Naoki
AU - Matsuura, Kumi
AU - Akiyama, Tomohiko
AU - Suzuki, Atsushi
AU - Niwa, Hitoshi
AU - Tachibana, Makoto
AU - Ohba, Takashi
AU - Katabuchi, Hidetaka
AU - Namekawa, Satoshi H.
AU - Araki, Kimi
AU - Ishiguro, Kei Ichiro
N1 - Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12/1
Y1 - 2021/12/1
N2 - During spermatogenesis, meiosis is accompanied by a robust alteration in gene expression and chromatin status. However, it remains elusive how the meiotic transcriptional program is established to ensure completion of meiotic prophase. Here, we identify a protein complex that consists of germ-cell-specific zinc-finger protein ZFP541 and its interactor KCTD19 as the key transcriptional regulators in mouse meiotic prophase progression. Our genetic study shows that ZFP541 and KCTD19 are co-expressed from pachytene onward and play an essential role in the completion of the meiotic prophase program in the testis. Furthermore, our ChIP-seq and transcriptome analyses identify that ZFP541 binds to and suppresses a broad range of genes whose function is associated with biological processes of transcriptional regulation and covalent chromatin modification. The present study demonstrates that a germ-cell specific complex that contains ZFP541 and KCTD19 promotes the progression of meiotic prophase towards completion in male mice, and triggers the reconstruction of the transcriptional network and chromatin organization leading to post-meiotic development.
AB - During spermatogenesis, meiosis is accompanied by a robust alteration in gene expression and chromatin status. However, it remains elusive how the meiotic transcriptional program is established to ensure completion of meiotic prophase. Here, we identify a protein complex that consists of germ-cell-specific zinc-finger protein ZFP541 and its interactor KCTD19 as the key transcriptional regulators in mouse meiotic prophase progression. Our genetic study shows that ZFP541 and KCTD19 are co-expressed from pachytene onward and play an essential role in the completion of the meiotic prophase program in the testis. Furthermore, our ChIP-seq and transcriptome analyses identify that ZFP541 binds to and suppresses a broad range of genes whose function is associated with biological processes of transcriptional regulation and covalent chromatin modification. The present study demonstrates that a germ-cell specific complex that contains ZFP541 and KCTD19 promotes the progression of meiotic prophase towards completion in male mice, and triggers the reconstruction of the transcriptional network and chromatin organization leading to post-meiotic development.
UR - http://www.scopus.com/inward/record.url?scp=85107427610&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85107427610&partnerID=8YFLogxK
U2 - 10.1038/s41467-021-23378-4
DO - 10.1038/s41467-021-23378-4
M3 - Article
C2 - 34075040
AN - SCOPUS:85107427610
SN - 2041-1723
VL - 12
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 3184
ER -