An age-related homeostasis mechanism is essential for spontaneous amelioration of hemophilia B Leyden

  • Sumiko Kurachi
    Age Dimension Research Center, National Institute of Advanced Industrial Science and Technology, Tsukuba, 305-8566 Japan; and
  • Jeffrey S. Huo
    Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan 48109-5618
  • Afshin Ameri
    Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan 48109-5618
  • Kezhong Zhang
    Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan 48109-5618
  • Akiyasu C. Yoshizawa
    Age Dimension Research Center, National Institute of Advanced Industrial Science and Technology, Tsukuba, 305-8566 Japan; and
  • Kotoku Kurachi
    Age Dimension Research Center, National Institute of Advanced Industrial Science and Technology, Tsukuba, 305-8566 Japan; and

書誌事項

公開日
2009-05-12
DOI
  • 10.1073/pnas.0902191106
公開者
Proceedings of the National Academy of Sciences

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説明

<jats:p>Regulation of age-related changes in gene expression underlies many diseases. We previously discovered the first puberty-onset gene switch, the age-related stability element (ASE)/age-related increase element (AIE)-mediated genetic mechanism for age-related gene regulation. Here, we report that this mechanism underlies the mysterious puberty-onset amelioration of abnormal bleeding seen in hemophilia B Leyden. Transgenic mice robustly mimicking the Leyden phenotype were constructed. Analysis of these animals indicated that ASE plays a central role in the puberty-onset amelioration of the disease. Human factor IX expression in these animals was reproducibly nullified by hypophysectomy, but nearly fully restored by administration of growth hormone, being consistent with the observed sex-independent recovery of factor IX expression. Ets1 was identified as the specific liver nuclear protein binding only to the functional ASE, G/CAGGAAG, and not to other Ets consensus elements. This study demonstrates the clinical relevance of the first discovered puberty-onset gene switch, the ASE/AIE-mediated regulatory mechanism.</jats:p>

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