2009 Fiscal Year Final Research Report
Molecular mechanism of synapsis checkpoint in mammalian meiosis
Project/Area Number |
20790169
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
General anatomy (including Histology/Embryology)
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Research Institution | Fujita Health University |
Principal Investigator |
KOGO Hiroshi Fujita Health University, 総合医科学研究所, 助教 (20282387)
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Project Period (FY) |
2008 – 2009
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Keywords | 減数分裂 / 不妊症 / 不育症 |
Research Abstract |
Meiosis is a special type of cell division producing oocytes and sperms. The failure in the process of meiosis causes infertility and miscarriage in human reproduction. To avoid such problems, there is a surveillance mechanism called meiotic checkpoint, although its molecular mechanism has been totally unknown, especially in mammals. In this study, the function of a meiosis-specific gene HORMAD1 was analyzed by generating gene-targeted mice. As a result, HORMAD1 was identified as the first gene required for the meiotic checkpoint in mammals.
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[Journal Article] Screening of genes involved in chromosome segregation during meiosis I: towards the identification of genes responsible for infertility in humans.2010
Author(s)
Kogo, H., Kowa- Sugiyama, H., Yamada, K., Bolor, H., Tsutsumi, M., Ohye, T., Inagaki, H., Taniguchi, M., Toda, T., Kurahashi, H.
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Journal Title
J. Hum. Genet. 55(5)
Pages: 293-299
Peer Reviewed
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[Journal Article] Paternal origin of the de novo constitutional t(11;22)(q23;q11).2010
Author(s)
Ohye, T., Inagaki, H., Kogo, H., Tsutsumi, M., Kato, T., Tong, M., Macville, M.V., Medne, L., Zackai, E.H., Emanuel, B.S. Kurahashi, H.
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Journal Title
Eur. J. Hum. Genet. (in press)
Peer Reviewed
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[Journal Article] Mutations of the SYCP3 gene in women with recurrent pregnancy loss.2009
Author(s)
Bolor, H., Mori, T., Nishiyama, S., Ito, Y., Hosoba, E., Inagaki, H., Kogo, H., 他11名
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Journal Title
Am. J. Hum. Genet. 84
Pages: 14-20
Peer Reviewed
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[Journal Article] Chromosomal instability mediated by non-B DNA: Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans.2009
Author(s)
Inagaki, H., Ohye, T., Kogo, H., Kato, T., Bolor, H., Taniguchi, M., Shaikh, T.H., Emanuel, B.S., Kurahashi, H.
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Journal Title
Genome Res. 19
Pages: 191-198
Peer Reviewed
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[Journal Article] Impaired DNA replication prompts deletions within palindromic sequences, but does not induce translocations in human cells.2009
Author(s)
Kurahashi, H. Inagaki, H., Kato, T., Hosoba, E., Kogo, H., Ohye, T., Tsutsumi, M., Bolor, H., Tong, M., Emanuel, B.S.
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Journal Title
Hum. Mol. Genet. 18
Pages: 3397-3406
Peer Reviewed
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[Journal Article] Recent advance in our understanding of the molecular nature of chromosomal abnormalities.2009
Author(s)
Kurahashi, H., Bolor, H., Kato, T., Kogo, H., Tsutsumi, M., Inagak i, H., Ohye, T.
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Journal Title
J Hum Genet. 54
Pages: 253-260
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[Journal Article] Increased levels of pregnancy-associated plasma protein-A2 in the serum of pre-eclamptic patients.2008
Author(s)
Nishizawa, H., Pryor-Koishi, K., Suzuki, M., Kato, T., Kogo, H., Sekiya, T., Kurahashi, H., Udagawa, Y.
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Journal Title
Mol. Hum. Reprod. 14
Pages: 595-602
Peer Reviewed
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