First case of aplastic anemia in a Japanese child with a homozygous missense mutation in the NBS1 gene (I171V) associated with genomic instability

Hiroyuki Shimada, Kimiko Shimizu, Sachiyo Mimaki, Tokuki Sakiyama, Tetsuya Mori, Noriko Shimasaki, Jun Yokota, Kei Nakachi, Tsutomu Ohta, Misao Ohki

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The NBS1 gene is strongly linked to several factors involved in genome integrity. Functional disruption of NBS1 could therefore induce genomic instability and carcinogenesis. Four children with acute lymphoblastic leukemia have been reported to be heterozygous for a germline and/or somatic missense mutation in NBS1, leading to the I171V substitution. We screened healthy controls and pediatric patients with hematological malignancies and aplastic anemia (AA) for the presence of I171V. Of the 62 patients, one individual with AA was confirmed to harbor a homozygous I171V mutation. Genetic analysis of NBS1 in this patient and her healthy parents indicated that she inherited the germline I171V mutation from her father and the wild-type allele from her mother, and that the second I171V hit occurred on the wild-type allele early in embryonic development. Furthermore, cytogenetic analysis of lymphoblastic cell lines from the patient indicated a remarkable increase in numerical and structural chromosomal aberrations in the absence of clastogens, suggesting that she potentially carried genomic instability. This is the first report of AA with a homozygous I171V mutation. We hypothesize that NBS1 may play an important role in the pathogenesis of AA.

Original languageEnglish
Pages (from-to)372-376
Number of pages5
JournalHuman Genetics
Issue number5
Publication statusPublished - 2004 Oct 1


ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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