Screening of no-coding RNA that can control transcription and chromatin
Project/Area Number |
16K14638
|
Research Category |
Grant-in-Aid for Challenging Exploratory Research
|
Allocation Type | Multi-year Fund |
Research Field |
Genome biology
|
Research Institution | Hokkaido University |
Principal Investigator |
Murakami Yota 北海道大学, 理学研究院, 教授 (20260622)
|
Co-Investigator(Renkei-kenkyūsha) |
TAKAHATA Shinya 北海道大学, 理学研究院, 助教 (50381588)
|
Project Period (FY) |
2016-04-01 – 2018-03-31
|
Project Status |
Completed (Fiscal Year 2017)
|
Budget Amount *help |
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2017: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2016: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
|
Keywords | non-coding RNA / 転写制御 / 分裂酵母 / スクリーニング / 遺伝子発現 / エピジェネティクス / 分裂区公募 |
Outline of Final Research Achievements |
To screen non-coding RNAs that have an ability to control transcription in fission yeast, we tried to construct a screening system using structure-specific RNA binding protein MS12 that enable tether non-coding RNAs to the promoter of reporter genes. However, we gave up to use MS12, because MS2 itself shows transcription stimulation activity. We next try to utilize CRISPR-dCAS9 to tether RNAs onto the promoter. We succeeded to recruit CRISPR-dCAS9 to the target region of fission yeast genome, but its efficiency is still low. We are trying to improve the efficiency.
|
Report
(3 results)
Research Products
(3 results)
-
-
-
[Journal Article] Inner nuclear membrane protein Lem2 augments heterochromatin formation in response to nutritional conditions.2016
Author(s)
Tange Y, Chikashige Y, Takahata S, Kawakami K, Higashi M, Mori C, Kojidani T, Hirano Y, Asakawa H, Murakami Y, Haraguchi T, Hiraoka Y.
-
Journal Title
Genes to Cells
Volume: 21
Issue: 8
Pages: 812-832
DOI
NAID
Related Report
Peer Reviewed / Open Access