Investigation of epigenetic therapeutic targets for musculoskeletal diseases
Project/Area Number |
15H04961
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Orthopaedic surgery
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Research Institution | Ehime University |
Principal Investigator |
Yuuki Imai 愛媛大学, プロテオサイエンスセンター, 教授 (10423873)
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Co-Investigator(Renkei-kenkyūsha) |
Inoue Kazuki 愛媛大学, 学術支援センター, 助教 (60623725)
Sakakibara Iori 愛媛大学, プロテオサイエンスセンター, 助教 (50734662)
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Project Period (FY) |
2015-04-01 – 2018-03-31
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Project Status |
Completed (Fiscal Year 2017)
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Budget Amount *help |
¥16,380,000 (Direct Cost: ¥12,600,000、Indirect Cost: ¥3,780,000)
Fiscal Year 2017: ¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2016: ¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2015: ¥5,720,000 (Direct Cost: ¥4,400,000、Indirect Cost: ¥1,320,000)
|
Keywords | エピジェネティクス / 軟骨 / ゲノムワイド解析 / エピジェネティック制御因子 / Uhrf1 / DNAメチル化 / 軟骨細胞 / 運動器 / 分化 / 遺伝子改変マウス |
Outline of Final Research Achievements |
The physiological functions of Uhrf1 in skeletal tissues remain unclear. We show that limb mesenchymal cell-specific Uhrf1 conditional knockout mice (cKO) exhibit remarkably shortened long bones that have morphological deformities due to dysregulated chondrocyte differentiation and proliferation. Especially, Mmp13 expression was significantly increased in both mRNA and protein levels in cKO mice. Integrative analyses using RNA-seq and MBD-seq revealed that Uhrf1 deficiency decreased genome-wide DNA methylation and increased gene expression through reduced DNA methylation in the promoter regions of 28 genes, including Hspb1. Hspb1 knockdown in cKO chondrocytes can normalize abnormal expression of genes involved in chondrocyte differentiation such as Mmp13. These results indicate that Uhrf1 governs cell-type specific transcriptional regulation by controlling the genome-wide DNA methylation status and regulating consequent cell differentiation and skeletal maturation.
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Report
(4 results)
Research Products
(29 results)
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[Journal Article] The HIV co-receptor CCR5 regulates osteoclast function.2017
Author(s)
Lee JW, Hoshino A, Inoue K, Saitou T, Uehara S, Kobayashi Y, Ueha S, Matsushima K, Yamaguchi A, Imai Y, Iimura T.
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Journal Title
Nat Commun
Volume: 8
Issue: 1
Pages: 2226-2226
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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[Journal Article] Genome-wide Association Study of Idiopathic Osteonecrosis of the Femoral Head2017
Author(s)
Sakamoto Y, Yamamoto T, Sugano N, Takahashi D, Watanabe T, Atsumi T, Nakamura J, Hasegawa Y, Akashi K, Narita I, Miyamoto T, Takeuchi T, Ikari K, Amano K, Fujie A, Kubo T, Tada Y, Kaneuji A, Nakamura H, Miyamura T, Kabata T, Yamaji K, Okawa T, Sudo A, Ohzono K, Tanaka Y, Yasunaga Y, Matsuda S, Imai Y
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Journal Title
Sci Rep.
Volume: 7
Issue: 1
Pages: 15035-15035
DOI
NAID
Related Report
Peer Reviewed / Open Access
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[Journal Article] The CUL3-SPOP-DAXX axis is a novel regulator of VEGFR2 expression in vascular endothelial cells2017
Author(s)
Sakaue T, Sakakibara I, Fujisaki A, Uesugi T, Nakashiro K, Hamakawa H, Kubota E, Joh T, Imai Y, Izutani H, Higashiyama S.
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Journal Title
Sci Rep.
Volume: 7
Issue: 1
Pages: 42845-42845
DOI
Related Report
Peer Reviewed / Open Access
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[Journal Article] Identification of Nedd9 as a TGF-β-Smad2/3 Target Gene Involved in RANKL-Induced Osteoclastogenesis by Comprehensive Analysis2016
Author(s)
Omata Y, Nakamura S, Koyama T, Yasui T, Hirose J, Izawa N, Matsumoto T, Imai Y, Seo S, Kurokawa M, Tsutsumi S, Kadono Y, Morimoto C, Aburatani H, Miyamoto T, Tanaka S.
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Journal Title
PLoS One.
Volume: 11
Issue: 6
Pages: e0157992-e0157992
DOI
Related Report
Peer Reviewed / Open Access
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[Presentation] エピゲノム制御因子Uhrf1によるDNAメチル化制御を介した軟骨分化・骨格形成2017
Author(s)
山下美智子,井上和樹,佐伯法学,榊原伊織,李智媛,大塚まき,亀井義明,五十嵐勝秀,高田泰次,飯村忠浩,今井祐記
Organizer
第35回日本骨代謝学会学術集会
Related Report
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