Studies on novel epigenetic regulator of the sex-determine in mammal
Project/Area Number |
16K18492
|
Research Category |
Grant-in-Aid for Young Scientists (B)
|
Allocation Type | Multi-year Fund |
Research Field |
Molecular biology
|
Research Institution | The University of Tokushima |
Principal Investigator |
OKASHITA Naoki 徳島大学, 先端酵素学研究所(次世代), 助教 (10757933)
|
Research Collaborator |
TACHIBANA Makoto 徳島大学, 先端酵素学研究所, 教授 (80303915)
|
Project Period (FY) |
2016-04-01 – 2018-03-31
|
Project Status |
Completed (Fiscal Year 2017)
|
Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2017: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2016: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
|
Keywords | 性決定 / エピジェネティクス / Sry |
Outline of Final Research Achievements |
In mammals, the sex-determining gene Sry on the Y chromosome initiates testis differentiation in embryonic gonads. Sry expression in gonads is fine-tuned in both space and time. We previously demonstrated that Histone H3 lysine 9 (H3K9) demethylation Jmjd1a plays an indispensable role in mouse sex development. However, little is known about epigenetic regulators other than Jmjd1a responsible for regulation of Sry expression. As a result of our analysis, methylcytosine dioxygenases (Tets), H3K9 methylases (Suv39h) and H3K9 methyl binders (HP1 family) played an important role in regulation of Sry expression.
|
Report
(3 results)
Research Products
(1 results)
-
[Journal Article] Rescuing the aberrant sex development of H3K9 demethylase Jmjd1a-deficient mice by modulating H3K9 methylation balance2017
Author(s)
Shunsuke Kuroki, Naoki Okashita, Baba Shoko, Maeda Ryo, Shingo Miyawaki, Masashi Yano, Yamaguchi Miyoko, Kitano Satsuki, Miyachi Hitoshi, Itoh Akihiro, Yoshida Minoru and Makoto Tachibana
-
Journal Title
PLoS Genetics
Volume: 13(9)
Issue: 9
Pages: 1-22
DOI
NAID
Related Report
Peer Reviewed / Open Access