• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Molecular epidemiological study ovalocytosis in Indonesia

Research Project

Project/Area Number 06041076
Research Category

Grant-in-Aid for international Scientific Research

Allocation TypeSingle-year Grants
SectionField Research
Research InstitutionKobe University

Principal Investigator

MATSUO Masafumi  Kobe University, School of Medicine, 医学部, 教授 (10157266)

Co-Investigator(Kenkyū-buntansha) SUMADIONO  Gadjah Mada University, Faculty of Medicine, 医学部, 講師
SEOATOMADJI  Airlangga University, Faculty of Medicine, 医学部, 教授
ABDUL Sofro  Gadjah Mada University, Faculty of Medicine, 医学部, 教授
NISHIO Hiashide  Kobe University, School of Medicine, 医学部, 助教授 (80189258)
ISHIDA Takafumi  University of Tokyo, Faculty of Science, 理学部, 助手 (20184533)
SHIRAKAWA Taku  Kobe University, School of Medicine, 医学部, 助手 (30171044)
NISHIYAMA Kaoru  Kobe University, School of Medicine, 医学部, 教授 (00150061)
ハルヂオノ  インドネシア大学, 医学部, 講師
スアトマジ  アイルランガ大学, 医学部, 教授
アブヅルソフロ  ガジャマダ大学, 医学部, 教授
Project Period (FY) 1994 – 1995
Project Status Completed (Fiscal Year 1995)
Budget Amount *help
¥5,900,000 (Direct Cost: ¥5,900,000)
Fiscal Year 1995: ¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 1994: ¥2,700,000 (Direct Cost: ¥2,700,000)
KeywordsOvalocytosis / Erythrocyte / Band 3 protein / Deletion mutation / Indonesia / 遺伝性楕円赤血球症 / バンド3蛋白遺伝子
Research Abstract

Southeast Asian ovalocytosis (SAO) is a hereditaty from of elliptocytosis resulting in rigid, oval-shaped erythrocytes resistant to invasion by malaria parasites. The molecular basis for SAO was recently identified as a heterogeneous presence of an altered erythrocyte band 3 protein, which lacked nine amino acids at the boundary between cytoplasmic and membrane domains. In order to clarify the mutation responsible for Indonesian ovalocytosis, we analyzed the erythrocyte band 3 protein gene of hereditary ovalocytosis in Rombok, Indonesia.
The Indonesian case was diagnosed to be ovalocytosis, because examination of his peripheral blood smear disclosed 75% of red blood cells were ovalocytic. DNA sample was extracted from blood cells and used as a template for PCR amplification. To determine a mutation in the band 3 gene, 175 bp long region spreading from nt. 1098 to 1272 of band 3 protein cDNA was amplified. From normal DNA only one band was visualized. In contrast, two narrowly separated bands were obtained from Indonesian ovalocytosis case i. e. ; the one slightly smaller than a control, the other comigrating with the control. These results showed that the index case is heterogeneous for the band 3 gene.
The amplified products were sequenced. Normal size product disclosed the sequence completely matched with that of wild type. The smaller amplified product had a 27 nucleotides deletion. These findings confirmed that the Indonesian ovalocyte is also heterozygous for the abnormal band 3 protein that has nine amino acids deletion.

Report

(2 results)
  • 1995 Final Research Report Summary
  • 1994 Annual Research Report
  • Research Products

    (9 results)

All Other

All Publications (9 results)

  • [Publications] Cutiongco,E.M.: "More deletions in the 5'region than in the central region of the dystrophin gene were identified among Filipino Duchenne and Becker muscular dystrophy patients." Am.J.Med.Genet.59. 266-267 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Shirakawa,T.: "Comparison of insertion rate of L1 retroposon into intron 30 of the neurofibromatosis type 1 gene in seven asian and pacific populations." (in press). (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Suryantoro,P.: "C to T transition at the first nucleotide of codon 63 of the b-globin gene corresponding to hemoglobin M-Saskatoon in an Indonesian boy." Jpn.J.Human Genet.40. 195-201 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Cutiongco, E.M.: "More deletions in the 5' region than in the central region of the dystrophin gene were identified among Filipino Duchenne and Becker muscular dystrophy patients." Am. J.Med. Genet.59. 266-267 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Shirakawa, T.: "Comparison of insertion rate of L1 retroposon into intron 30 of the neurofibromatosis type 1 gene in seven asian and pacific populations." Jpn. J.Hum. Genet.(in press.). (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Suryantoro, P.: "C to T transition at the first nucleotide of codon 63 of the b-globin gene corresponding to hemoglobin M-Saskatoon in an Indonesian boy." Jpn. J.Human Genet.40. 195-201 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Hagiwara,Y.: "A novel point mutation (G-1 to T)in a 5'splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy." Am.J.Hum.Genet.54. 53-61 (1994)

    • Related Report
      1994 Annual Research Report
  • [Publications] Nishio,H.: "Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter." J.Clin.Invest.94. 1037-1042 (1994)

    • Related Report
      1994 Annual Research Report
  • [Publications] Takeshima,Y.: "Twenty seven nucleotide deletion within exon 11 of the erythrocyte Band 3 gene in lndonesian ovalocytosis." Jpn.J.Hum.Genet.39. 181-185 (1994)

    • Related Report
      1994 Annual Research Report

URL: 

Published: 1994-04-01   Modified: 2016-04-21  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi