Journal article
C19ORF84 connects piRNA and DNA methylation machineries to defend the mammalian germ line
- Abstract:
- In the male mouse germ line, PIWI-interacting RNAs (piRNAs), bound by the PIWI protein MIWI2 (PIWIL4), guide DNA methylation of young active transposons through SPOCD1. However, the underlying mechanisms of SPOCD1-mediated piRNA-directed transposon methylation and whether this pathway functions to protect the human germ line remain unknown. We identified loss-of-function variants in human SPOCD1 that cause defective transposon silencing and male infertility. Through the analysis of these pathogenic alleles, we discovered that the uncharacterized protein C19ORF84 interacts with SPOCD1. DNMT3C, the DNA methyltransferase responsible for transposon methylation, associates with SPOCD1 and C19ORF84 in fetal gonocytes. Furthermore, C19ORF84 is essential for piRNA-directed DNA methylation and male mouse fertility. Finally, C19ORF84 mediates the in vivo association of SPOCD1 with the de novo methylation machinery. In summary, we have discovered a conserved role for the human piRNA pathway in transposon silencing and C19ORF84, an uncharacterized protein essential for orchestrating piRNA-directed DNA methylation.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Access Document
- Files:
-
-
(Preview, Version of record, pdf, 6.0MB, Terms of use)
-
- Publisher copy:
- 10.1016/j.molcel.2024.01.014
Authors
- Publisher:
- Cell Press
- Journal:
- Molecular Cell More from this journal
- Volume:
- 84
- Issue:
- 6
- Pages:
- 1021-1035.e11
- Place of publication:
- United States
- Publication date:
- 2024-02-14
- Acceptance date:
- 2024-01-17
- DOI:
- EISSN:
-
1097-4164
- ISSN:
-
1097-2765
- Pmid:
-
38359823
- Language:
-
English
- Keywords:
- Pubs id:
-
1620391
- Local pid:
-
pubs:1620391
- Deposit date:
-
2025-05-27
- ARK identifier:
Terms of use
- Copyright holder:
- Zoch et al
- Copyright date:
- 2024
- Rights statement:
- © 2024 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
- Licence:
- CC Attribution (CC BY)
If you are the owner of this record, you can report an update to it here: Report update to this record