Mechanisms of male-type differentiation in mouse primordial germ cells
Project/Area Number |
26440120
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Developmental biology
|
Research Institution | Yokohama National University |
Principal Investigator |
Suzuki Atsushi 横浜国立大学, 大学院工学研究院, 准教授 (60467058)
|
Research Collaborator |
NIIMI Yuki
|
Project Period (FY) |
2014-04-01 – 2017-03-31
|
Project Status |
Completed (Fiscal Year 2016)
|
Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2016: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
|
Keywords | 生殖細胞 / Nanos / Dead end / 精巣テラトーマ / 潜在的な分化多能性 / 精巣性テラトーマ / 始原生殖細胞 / テラトーマ / RNA結合タンパク質 |
Outline of Final Research Achievements |
Mouse NANOS2 suppresses ectopic meiosis and promotes male-type gene expression, playing a critical role in sexual differentiation of primordial germ cells. However, the mechanisms involved in target specificity remain elusive. We show that another RBP, Dead end1 (DND1), directly interacts with NANOS2 to load unique RNAs into the CNOT complex. Thus, DND1 is an essential partner for NANOS2 that leads to the degradation of specific RNAs.
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Report
(4 results)
Research Products
(7 results)