Setdb1 is required for germline development and silencing of H3K9me3-marked endogenous retroviruses in primordial germ cells

Sheng Liu, Julie Brind’Amour, Mohammad M. Karimi, Kenjiro Shirane, Aaron Bogutz, Louis Lefebvre, Hiroyuki Sasaki, Yoichi Shinkai, Matthew C. Lorincz

Research output: Contribution to journalArticle

94 Citations (Scopus)

Abstract

Transcription of endogenous retroviruses (ERVs) is inhibited by de novo DNA methylation during gametogenesis, a process initiated after birth in oocytes and at approximately embryonic day 15.5 (E15.5) in prospermatogonia. Earlier in germline development, the genome, including most retrotransposons, is progressively demethylated. Young ERVK and ERV1 elements, however, retain intermediate methylation levels. As DNA methylation reaches a low point in E13.5 primordial germ cells (PGCs) of both sexes, we determined whether retrotransposons are marked by H3K9me3 and H3K27me3 using a recently developed low-input ChIP-seq (chromatin immunoprecipitation [ChIP] combined with deep sequencing) method. Although these repressive histone modifications are found predominantly on distinct genomic regions in E13.5 PGCs, they concurrently mark partially methylated long terminal repeats (LTRs) and LINE1 elements. Germline-specific conditional knockout of the H3K9 methyltransferase SETDB1 yields a decrease of both marks and DNA methylation at H3K9me3-enriched retrotransposon families. Strikingly, Setdb1 knockout E13.5 PGCs show concomitant derepression of many marked ERVs, including intracisternal A particle (IAP), ETn, and ERVK10C elements, and ERV-proximal genes, a subset in a sex-dependent manner. Furthermore, Setdb1 deficiency is associated with a reduced number of male E13.5 PGCs and postnatal hypogonadism in both sexes. Taken together, these observations reveal that SETDB1 is an essential guardian against proviral expression prior to the onset of de novo DNA methylation in the germline.

Original languageEnglish
Pages (from-to)2041-2055
Number of pages15
JournalGenes and Development
Volume28
Issue number18
DOIs
Publication statusPublished - 15 Sep 2014
Externally publishedYes

Fingerprint

Endogenous Retroviruses
DNA Methylation
Germ Cells
Retroelements
Chromatin Immunoprecipitation
Histone Code
Gametogenesis
High-Throughput Nucleotide Sequencing
Hypogonadism
Terminal Repeat Sequences
Methyltransferases
Methylation
Oocytes
Parturition
Genome
Genes

Keywords

  • DNA methylation
  • Endogenous retroviruses
  • Germ cell development
  • H3K27me3
  • H3K9me3
  • Setdb1

ASJC Scopus subject areas

  • Genetics
  • Developmental Biology

Cite this

Setdb1 is required for germline development and silencing of H3K9me3-marked endogenous retroviruses in primordial germ cells. / Liu, Sheng; Brind’Amour, Julie; Karimi, Mohammad M.; Shirane, Kenjiro; Bogutz, Aaron; Lefebvre, Louis; Sasaki, Hiroyuki; Shinkai, Yoichi; Lorincz, Matthew C.

In: Genes and Development, Vol. 28, No. 18, 15.09.2014, p. 2041-2055.

Research output: Contribution to journalArticle

Liu, S, Brind’Amour, J, Karimi, MM, Shirane, K, Bogutz, A, Lefebvre, L, Sasaki, H, Shinkai, Y & Lorincz, MC 2014, 'Setdb1 is required for germline development and silencing of H3K9me3-marked endogenous retroviruses in primordial germ cells', Genes and Development, vol. 28, no. 18, pp. 2041-2055. https://doi.org/10.1101/gad.244848.114
Liu, Sheng ; Brind’Amour, Julie ; Karimi, Mohammad M. ; Shirane, Kenjiro ; Bogutz, Aaron ; Lefebvre, Louis ; Sasaki, Hiroyuki ; Shinkai, Yoichi ; Lorincz, Matthew C. / Setdb1 is required for germline development and silencing of H3K9me3-marked endogenous retroviruses in primordial germ cells. In: Genes and Development. 2014 ; Vol. 28, No. 18. pp. 2041-2055.
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AU - Shirane, Kenjiro

AU - Bogutz, Aaron

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