a molecular biology study of Autosomal dominant tubulointerstitial kidney disease by using mutated MUC1 cDNA sequence identified in our own patient family.
| Project/Area Number |
16K09615
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Kidney internal medicine
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| Research Institution | Osaka University |
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Principal Investigator |
Kaimori Junya 大阪大学, 医学系研究科, 寄附講座准教授 (70527697)
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| Co-Investigator(Kenkyū-buntansha) |
猪阪 善隆 大阪大学, 医学系研究科, 教授 (00379166)
高原 史郎 大阪大学, 医学系研究科, 招へい教授 (70179547)
市丸 直嗣 大阪大学, 医学系研究科, 寄附講座准教授 (70346211)
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| Project Period (FY) |
2016-04-01 – 2019-03-31
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| Project Status |
Completed (Fiscal Year 2018)
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| Budget Amount *help |
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2018: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2017: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2016: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
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| Keywords | ADTKD / MUC1 / VNTR / 小胞体ストレス / 細胞内凝集 / transgenic mouse / ER stress / 家族性尿細管間質腎炎 / 次世代シークエンサー / 全エクソーム解析 / 腎臓内科 / 家族性疾患 / 尿細管間質腎炎 / 腎臓学 |
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| Outline of Final Research Achievements |
Autosomal dominant tublointerstitial kidney disease (ADTKD) is an inherited kidney disease characterized by the progressive renal function loss almost without no urine sedimentation findings. Almost all previous gene mutation sites in ADTKD-MUC1 were placed within variable number tandem repeats (VNTRs). We discovered ADTKD-MUC1 family whose mutation site was before VNTRs. We also discovered that mutant MUC1 protein was resulted in cytoplasmic aggregation. Furtherly, we made mutant human MUC1 transgenic mouse and found that these mice demonstrated systemic inflammatory disease. In the response to these transgenic mouse findings, re-examination in our patients revealed that they also had interstitial pneumonia, inflammatory bowel disease, and skin lesion, which had not been described as symptoms of ADTKD-MUC1.
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| Academic Significance and Societal Importance of the Research Achievements |
従来、ADTKD-MUC1の遺伝子異常部位は、VNTRに限られており、世界的にもVNTR以外のMUC1異常は報告されてこなかった。今症例は、VNTR以前に異常のある症例であり、症例的な意義は高い。また、ADTKD-MUC1の腎外病変については、今まで世界でも報告された事は無く、ADTKD-MUC1には、腎外病変はないとされてきた。申請者らの、transgenic mouse及び患者家系における、腎外病変の発見は、ADTKD-MUC1の病態像を根底から書き換えるもので、臨床的な意義は極めて高い。
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Report
(4 results)
Research Products
(11 results)
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[Journal Article] Analysis of an ADTKD family with a novel frameshift mutation in MUC1 reveals characteristic features of mutant MUC1 protein2017
Author(s)
Yamamoto S, Kaimori J, Yoshimura T, Namba T, Imai A, Kobayashi K, Imamura R, Ichimaru N, Kato K, Nakaya A, Takahara S, & Isaka Y
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Journal Title
Nephrology Dialysis Transplantation
Volume: 32
Issue: 12
Pages: 2010-2007
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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[Journal Article] Analysis of an ADTKD family with a novel frameshift mutation in MUC1 reveals characteristic features of mutant MUC1 protein2017
Author(s)
Satoko Yamamoto, Jun-Ya Kaimori, Takuji Yoshimura, Tomoko Namba, Atsuko Imai, Kaori Kobayashi, Ryoichi Imamura, Naotsugu Ichimaru, Kazuto Kato, Akihiro Nakaya, Shiro Takahara, Yoshitaka Isaka
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Journal Title
Ｎｅｐｈｒｏｌｏｇｙ Ｄｉａｌｙｓｉｓ Ｔｒａｎｓｐｌａｎｔａｔｉｏｎ
Volume: ｉｎ ｐｒｅｓｓ
Related Report
Peer Reviewed / Int'l Joint Research / Acknowledgement Compliant
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