4.3 Article

Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR

Journal

EPIGENETICS & CHROMATIN
Volume 11, Issue -, Pages -

Publisher

BIOMED CENTRAL LTD
DOI: 10.1186/s13072-018-0200-6

Keywords

DMR; DNA methylation; Genomic imprinting

Funding

  1. Japan Society for the Promotion of Science [16K09970, 17K08687]
  2. Japan Agency for Medical Research and Development (AMED) [17ek0109280h0001, 17ek0109234h0001, 17ek0109205h0001]
  3. National Center for Child Health and Development [26-13]
  4. Ministry of Health, Labor, and Welfare [H29-nanchitou(nan)-ippan-025]
  5. joint research program of the Institute for Molecular and Cellular Regulation, Gunma University [16029]
  6. Grants-in-Aid for Scientific Research [17K08687, 16K09970] Funding Source: KAKEN

Ask authors/readers for more resources

Background: Zrsr1 is a paternally expressed imprinted gene located in the first intron of Commdl, and the Zrsr1 promoter resides in a differentially methylated region (DMR) that is maternally methylated in the oocyte. However, a mechanism for the establishment of the methylation has remained obscure. Commdl is transcribed in the opposite direction to Zrsr1 with predominant maternal expression, especially in the adult brain. Results: We found Commedl transcribed through the DMR in the growing oocyte. Zrsr1-DMR methylation was abolished by the prevention of Commdl transcription. Furthermore, methylation did not occur at the artificially unmethylated maternal Zrsr1-DMR during embryonic development when transcription through the DMR was restored in the zygote. Loss of methylation at the maternal Zrsr1-DMR resulted in biallelic Zrsr1 expression and reduced the extent of the predominant maternal expression of Commdl. Conclusions: These results indicate that the establishment of methylation at Zrsr1-DMR occurs in a transcriptiondependent and oocyte-specific manner and caused Zrsr1 imprinting by repressing maternal expression. The predominant maternal expression of Commdl is likely caused by transcriptional interference by paternal Zrsr1 expression.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available