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Identification of Genes Involved in the Severity of Alport Syndrome and Elucidation of the Mechanism of its Severity

Research Project

Project/Area Number 17H04189
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Kidney internal medicine
Research InstitutionKobe University

Principal Investigator

Iijima Kazumoto  神戸大学, 医学研究科, 教授 (00240854)

Co-Investigator(Kenkyū-buntansha) 高岡 裕  神戸大学, 医学部附属病院, 准教授 (20332281)
野津 寛大  神戸大学, 医学研究科, 特命教授 (70362796)
Project Period (FY) 2017-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥16,770,000 (Direct Cost: ¥12,900,000、Indirect Cost: ¥3,870,000)
Fiscal Year 2019: ¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2018: ¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2017: ¥7,150,000 (Direct Cost: ¥5,500,000、Indirect Cost: ¥1,650,000)
Keywordsアルポート症候群 / 重症化機序 / エクソンスキッピング / 腎臓学
Outline of Final Research Achievements

It was confirmed that there was no correlation in clinical feature and genotype in the X-linked Alport syndrome (XLAS) female patients. Furthermore, since no disease-modifying gene mutations were identified in most severely ill patients, the severity of female XLAS patients was considered to be multifactorial. Molecular simulation analysis of the α3,4,5 (IV) chain revealed that when the exon with the stop codon was skipped, the α3,4,5 (IV) chain with COL4A5 truncating mutations showed three-dimensional structure similar to that of the normal α3,4,5 (IV) chain. These results strongly suggest that the modification of the truncating mutation to the non-truncating mutation by exon skipping therapy may attenuate XLAS. We also found that the severity of patients with COL4A5 missense mutations was correlated to the ability of the α3,4,5 (IV) chain to form trimers.

Academic Significance and Societal Importance of the Research Achievements

我々は、今回の研究結果をもとに、XLASのエソンスキッピング療法の開発に着手しており、XLASモデルマウスを用いた治療研究で、エクソンスキッピング療法が非常に有効であることを世界で初めて明らかにしており(Nat Commun. in press)、近々に臨床試験を開始する予定である。

Report

(4 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Annual Research Report
  • 2017 Annual Research Report
  • Research Products

    (29 results)

All 2019 2018 2017 2016

All Journal Article (14 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 12 results,  Open Access: 7 results) Presentation (15 results) (of which Int'l Joint Research: 4 results,  Invited: 2 results)

  • [Journal Article] アルポート症候群2019

    • Author(s)
      野津寛大、飯島一誠
    • Journal Title

      指定難病ペディア,日本医師会雑誌

      Volume: 148 Pages: 249-249

    • Related Report
      2019 Annual Research Report
  • [Journal Article] Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome.2019

    • Author(s)
      Yamamura T, Nozu K, Minamikawa S, Horinouchi T, Sakakibara N, Nagano C, Aoto Y, Ishiko S, Nakanishi K, Shima Y, Nagase H, Rossanti R, Ye MJ, Nozu Y, Ishimori S, Morisada N, Kaito H, Iijima K.
    • Journal Title

      Mol Genet Genomic Med.

      Volume: 7(9) Issue: 9

    • DOI

      10.1002/mgg3.883

    • NAID

      120006733124

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay.2019

    • Author(s)
      Horinouchi T, Nozu K, Yamamura T, Minamikawa S, Nagano C, Sakakibara N, Nakanishi K, Shima Y, Morisada N, Ishiko S, Aoto Y, Nagase H, Takeda H, Rossanti R, Kaito H, Matsuo M, Iijima K.
    • Journal Title

      Sci Rep.

      Volume: 9(1) Issue: 1 Pages: 12696-12696

    • DOI

      10.1038/s41598-019-48990-9

    • NAID

      120006825910

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Establishment of X-linked Alport syndrome model mice with a Col4a5 R471X mutation2019

    • Author(s)
      Hashikami Kentarou、Asahina Makoto、Nozu Kandai、Iijima Kazumoto、Nagata Michio、Takeyama Michiyasu
    • Journal Title

      Biochemistry and Biophysics Reports

      Volume: 17 Pages: 81-86

    • DOI

      10.1016/j.bbrep.2018.12.003

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] A review of clinical characteristics and genetic backgrounds in Alport syndrome2018

    • Author(s)
      Nozu K, Nakanishi K, Abe Y, Udagawa T, Okada S, Okamoto T, Kaito H, Kanemoto K, Kobayashi A, Tanaka E, Tanaka K, Hama T, Fujimaru R, Miwa S, Yamamura T, Yamamura N, Horinouchi T, Minamikawa S, Nagata M, Iijima K
    • Journal Title

      Clinical and Experimental Nephrology

      Volume: 23 Issue: 2 Pages: 158-168

    • DOI

      10.1007/s10157-018-1629-4

    • NAID

      120006557458

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Germline mosaicism is a pitfall in the diagnosis of “sporadic” X-linked Alport syndrome2018

    • Author(s)
      Okamoto Takayuki、Nozu Kandai、Iijima Kazumoto、Ariga Tadashi
    • Journal Title

      Journal of Nephrology

      Volume: 32 Issue: 1 Pages: 155-159

    • DOI

      10.1007/s40620-018-0518-y

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome.2018

    • Author(s)
      Horinouchi T, Nozu K, Yamamura T, Minamikawa S, Omori T, Nakanishi K, Fujimura J, Ashida A, Kitamura M, Kawano M, Shimabukuro W, Kitabayashi C, Imafuku A, Tamagaki K, Kamei K, Okamoto K, Fujinaga S, Oka M, Igarashi T, Miyazono A, Sawanobori E, Fujimaru R, Nakanishi K, Shima Y et al
    • Journal Title

      J Am Soc Nephrol.

      Volume: 29 Issue: 8 Pages: 2244-2254

    • DOI

      10.1681/asn.2018030228

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] 【腎臓学 この一年の進歩】 遺伝性腎疾患2018

    • Author(s)
      野津 寛大, 飯島 一誠
    • Journal Title

      日本腎臓学会誌

      Volume: 61巻1号 Pages: 18-22

    • Related Report
      2018 Annual Research Report
  • [Journal Article] Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases2018

    • Author(s)
      Nagano C, Nozu K, Morisada N, Yazawa M, Ichikawa D, Numasawa K, Kourakata H, Matsumura C, Tazoe S, Tanaka R, Yamamura T, Minamikawa S, Horinouchi T, Nakanishi K, Fujimura J, Sakakibara N, Nozu Y, Ye MJ, Kaito H, Iijima K
    • Journal Title

      Clinical and Experimental Nephrology

      Volume: 印刷中 Issue: 4 Pages: 881-888

    • DOI

      10.1007/s10157-018-1534-x

    • NAID

      120006624236

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Natural History and Genotype?Phenotype Correlation in Female X-Linked Alport Syndrome2017

    • Author(s)
      Yamamura Tomohiko、Nozu Kandai、Fu Xue Jun、Nozu Yoshimi、Ye Ming Juan、Shono Akemi、Yamanouchi Satoko、Minamikawa Shogo、Morisada Naoya、Nakanishi Koichi、Shima Yuko、Yoshikawa Norishige、Ninchoji Takeshi、Morioka Ichiro、Kaito Hiroshi、Iijima Kazumoto
    • Journal Title

      Kidney Int Rep.

      Volume: 2 Issue: 5 Pages: 850-855

    • DOI

      10.1016/j.ekir.2017.04.011

    • NAID

      120006373817

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] A case of mild phenotype Alport syndrome caused by COL4A3 mutations2017

    • Author(s)
      Kamijo Masafumi、Kitamura Mineaki、Muta Kumiko、Uramatsu Tadashi、Obata Yoko、Nozu Kandai、Kaito Hiroshi、Iijima Kazumoto、Mukae Hiroshi、Nishino Tomoya
    • Journal Title

      CEN Case Reports

      Volume: 6 Issue: 2 Pages: 189-193

    • DOI

      10.1007/s13730-017-0273-2

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically2017

    • Author(s)
      Imafuku Aya、Nozu Kandai、Sawa Naoki、Hasegawa Eiko、Hiramatsu Rikako、Kawada Masahiro、Hoshino Junichi、Tanaka Kiho、Ishii Yasuo、Takaichi Kenmei、Fujii Takeshi、Ohashi Kenichi、Iijima Kazumoto、Ubara Yoshifumi
    • Journal Title

      Nephrology

      Volume: 印刷中 Issue: 10 Pages: 940-947

    • DOI

      10.1111/nep.13115

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis.2017

    • Author(s)
      Nozu K, Minamikawa S, Yamada S, Oka M, Yanagita M, Morisada N, Fujinaga S, Nagano C, Gotoh Y, Takahashi E, Morishita T, Yamamura T, Ninchoji T, Kaito H, Morioka I, Nakanishi K, Vorechovsky I, Iijima K
    • Journal Title

      J Hum Genet.

      Volume: Epub 2017 Mar 9. Issue: 7 Pages: 733-735

    • DOI

      10.1038/jhg.2017.28

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Int'l Joint Research
  • [Journal Article] Female X-linked Alport syndrome with somatic mosaicism2016

    • Author(s)
      Yokota K, Nozu K, Minamikawa S, Yamamura T, Nakanishi K, Kaneda H, Hamada R, Nozu Y, Shono A, Ninchoji T, Morisada N, Ishimori S, Fujimura J, Horinouchi T, Kaito H, Nakanishi K, Morioka I, Taniguchi-Ikeda M, Iijima K.
    • Journal Title

      Clin Exp Nephrol.

      Volume: 印刷中 Issue: 5 Pages: 877-883

    • DOI

      10.1007/s10157-016-1352-y

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Open Access
  • [Presentation] 遺伝性腎疾患に対するプレシジョンメディスン アルポート症候群に対する遺伝子標的療法の開発2019

    • Author(s)
      野津寛大、山村智彦、飯島一誠
    • Organizer
      第54回日本小児腎臓病学会学術集会
    • Related Report
      2019 Annual Research Report
    • Invited
  • [Presentation] 常染色体劣性Alport症候群39家系46人の臨床遺伝学的検討2019

    • Author(s)
      堀之内智子、野津寛大、石河慎也、青砥悠哉、 榊原菜々、長野智那、南川将吾、山村智彦、 貝藤裕史、森貞直哉、飯島一誠
    • Organizer
      第54回日本小児腎臓病学会学術集会
    • Related Report
      2019 Annual Research Report
  • [Presentation] Alport症候群モデルマウスにおけるエクソンスキッピング療法の有効性の検討2019

    • Author(s)
      山村智彦、野津寛大、堀之内智子、南川将吾、 足立朝美、寺川真紀、永瀬弘之、高石巨澄、 大西朗之、小路貴生、小泉誠、神田祥一郎、 張田豊、嘉村美里、甲斐広文、飯島一誠
    • Organizer
      第54回日本小児腎臓病学会学術集会
    • Related Report
      2019 Annual Research Report
  • [Presentation] 常染色体劣性Alport症候群39家系46人の臨床遺伝学的検討2019

    • Author(s)
      堀之内智子、野津寛大、榊原菜々、長野智那、南川将吾、山村智彦、飯島一誠
    • Organizer
      第62回日本腎臓学会学術集会
    • Related Report
      2019 Annual Research Report
  • [Presentation] Exon skipping therapy for COL4A5 gene truncating variant rescued progression of kidney failure in X-linked Alport syndrome2019

    • Author(s)
      Tomohiko Yamamura, Kandai Nozu, Kazumoto Iijima
    • Organizer
      American Society of Nephrology Kidney week 2019
    • Related Report
      2019 Annual Research Report
    • Int'l Joint Research
  • [Presentation] Splicing assay with hybrid minigene: assessing pathogenicities in COL4A5 intronic mutations2018

    • Author(s)
      Horinouchi T, Nozu K, Yamamura T, Sakakibara N, Nagano C, Nakanishi K, Fujimura J, Minamikawa S, Ninchoji T, Kaito H, Shima Y, Nakanishi K, Iijima K
    • Organizer
      52st Annual Meeting of the American Society of Nephrology
    • Related Report
      2018 Annual Research Report
    • Int'l Joint Research
  • [Presentation] Factors regulating the severity in male X-linked Alport syndrome: study of 367 cases2018

    • Author(s)
      Yamamura T, Nozu K, Sakakibara N, Nagano C, Fujimura J, Horinouchi T, Nakanishi K, Minamikawa S, Kaito H, Shima Y, Nakanishi K, Iijima K
    • Organizer
      52st Annual Meeting of the American Society of Nephrology
    • Related Report
      2018 Annual Research Report
    • Int'l Joint Research
  • [Presentation] 次世代シークエンサーを用いたAlport症候群の網羅的診断法の確立2018

    • Author(s)
      山村 智彦、野津 寛大、長野 智那、榊原 菜々、藤村 順也、堀之内 智子、中西 啓太、南川 将吾、貝藤 裕史、飯島 一誠
    • Organizer
      第121回日本小児科学会学術集会
    • Related Report
      2018 Annual Research Report
  • [Presentation] X染色体連鎖型Alport症候群男性患者341名の臨床遺伝学的検討2018

    • Author(s)
      山村 智彦、野津 寛大、榊原 菜々、長野 智那、藤村 順也、堀之内 智子、中西 啓太、南川 将吾、貝藤 裕史、中西 浩一、飯島 一誠
    • Organizer
      第61回日本腎臓学会学術総会
    • Related Report
      2018 Annual Research Report
  • [Presentation] Genotype-phenotype correlation in male X-linked Alport syndrome: 341 cases study2018

    • Author(s)
      Yamamura T, Sakakibara N, Nagano C, Nozu K, Fujimura J, Horinouchi T, Nakanishi K, Minamikawa S, Kaito H, Iijima K
    • Organizer
      第53回小児腎臓病学会学術集会
    • Related Report
      2018 Annual Research Report
  • [Presentation] カレント・トピック4 小児腎疾患における遺伝医学のトピックス2018

    • Author(s)
      飯島一誠
    • Organizer
      日本人類遺伝学会第63回大会
    • Related Report
      2018 Annual Research Report
    • Invited
  • [Presentation] A comprehensive diagnosis by targeted sequencing for clinically suspectsd alport syndrome patients in Japan2017

    • Author(s)
      Yamamura T, Nozu K, Fujimura J, Horinouchi T, Nakanishi K, Minamikawa S, Shono A, Ninchoji T, Kaito H, Shima Y, Nakanishi K, Iijima K.
    • Organizer
      Asian Congress of Pediatric Nephrology 2017 & 39th Malaysian Pediatric Association Annual Congress, Kuala Lumpur, Malaysia
    • Related Report
      2017 Annual Research Report
    • Int'l Joint Research
  • [Presentation] 次世代シークエンサーを用いたAlport症候群の網羅的診断法の確立2017

    • Author(s)
      山村智彦、野津寛大、藤村順也、堀之内智子、中西啓太、南川将吾、庄野朱美、忍頂寺毅史、貝藤裕史、中西浩一、飯島一誠
    • Organizer
      第60回日本腎臓学会 仙台
    • Related Report
      2017 Annual Research Report
  • [Presentation] エクソンスキッピング療法によるアルポート症候群特異的療法治療法の開発2017

    • Author(s)
      庄野朱美、野津寛大、小泉 誠、大西朗之、高石巨澄、山村智彦、南川将吾、飯島一誠
    • Organizer
      第52回日本小児腎臓病学会 東京
    • Related Report
      2017 Annual Research Report
  • [Presentation] Establishment of a comprehensive diagnostic method using next generation sequencer for the Alport syndrome2017

    • Author(s)
      Yamamura T, Nozu K, Fujimura J, Horinouchi T, Nakanishi K, Manamikawa S, Shono A, Ninchoji T, Kaito H, Nakanishi K, Iijima K
    • Organizer
      第52回日本小児腎臓病学会 東京
    • Related Report
      2017 Annual Research Report

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Published: 2017-04-28   Modified: 2021-02-19  

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