TY - JOUR
T1 - Sequences in the H19 ICR that are transcribed as small RNA in oocytes are dispensable for methylation imprinting in YAC transgenic mice
AU - Takahashi, Takuya
AU - Matsuzaki, Hitomi
AU - Tomizawa, Shin ichi
AU - Okamura, Eiichi
AU - Ichiyanagi, Tomoko
AU - Fukamizu, Akiyoshi
AU - Sasaki, Hiroyuki
AU - Tanimoto, Keiji
N1 - Funding Information:
We thank Dr. Doug Engel (University of Michigan) for critically reading this manuscript and Y. Tanimoto for outstanding technical assistance. E. O. is a research fellow of the Japan Society for the Promotion of Science. This work was supported by research grants from a Grant-in-Aid for Young Scientists (S) from the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT) to K. T. The work was also supported by a Grant-in-Aid for Scientific Research on Priority Area from the MEXT to H.S.
PY - 2012/10/15
Y1 - 2012/10/15
N2 - Allele-specific methylation of the endogenous H19 imprinting control region (ICR) is established in sperm. We previously showed that the paternal H19 ICR in yeast artificial chromosome (YAC) transgenic mice (TgM) was preferentially methylated in somatic cells, but not in germ cells, suggesting that differential methylation could be established after fertilization. In this report, we discovered small RNA molecules in growing oocytes, the nucleotide sequences of which mapped to the H19 ICR. To test if these small RNA sequences play a role in the establishment of differential methylation, we deleted the sequences from the H19 ICR DNA and generated YAC TgM. In somatic cells of these mice, methylation imprinting of the transgene was normally established. In addition, the mutant fragment was not methylated in sperm and eggs. These data demonstrate that sequences in the H19 ICR that correspond to the small RNA sequences are dispensable for methylation imprinting in YAC TgM.
AB - Allele-specific methylation of the endogenous H19 imprinting control region (ICR) is established in sperm. We previously showed that the paternal H19 ICR in yeast artificial chromosome (YAC) transgenic mice (TgM) was preferentially methylated in somatic cells, but not in germ cells, suggesting that differential methylation could be established after fertilization. In this report, we discovered small RNA molecules in growing oocytes, the nucleotide sequences of which mapped to the H19 ICR. To test if these small RNA sequences play a role in the establishment of differential methylation, we deleted the sequences from the H19 ICR DNA and generated YAC TgM. In somatic cells of these mice, methylation imprinting of the transgene was normally established. In addition, the mutant fragment was not methylated in sperm and eggs. These data demonstrate that sequences in the H19 ICR that correspond to the small RNA sequences are dispensable for methylation imprinting in YAC TgM.
UR - http://www.scopus.com/inward/record.url?scp=84865574325&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84865574325&partnerID=8YFLogxK
U2 - 10.1016/j.gene.2012.07.062
DO - 10.1016/j.gene.2012.07.062
M3 - Article
C2 - 22890135
AN - SCOPUS:84865574325
SN - 0378-1119
VL - 508
SP - 26
EP - 34
JO - Gene
JF - Gene
IS - 1
ER -