2002 Fiscal Year Final Research Report Summary
POSITIONAL CLONING OF HEREDITARY CATARACTS IN MICE
| Project/Area Number |
13480281
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Laboratory animal science
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| Research Institution | KYOTO UNIVERSITY |
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Principal Investigator |
HIRAI Hiroshi Kyoto University Graduate School of Medicine, Dept. Pathology & Biology of Diseases, Professor, 医学研究科, 教授 (10073131)
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| Co-Investigator(Kenkyū-buntansha) |
TACHIBANA Masayoshi Saitama Cancer Center, Research Laboratory, Chief, 研究主幹 (10128712)
YAMADA Yoshihiro Kyoto University Graduate School of Medicine, Dept. Pathology & Biology of Diseases, Lecturer, 医学研究科, 講師 (30252464)
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| Project Period (FY) |
2001 – 2002
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| Keywords | Hereditary cataract / Mouse / Lens / Positional cloning / Modifier gene |
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| Research Abstract |
We performed positional cloning of the genes responsible for two mouse hereditary cataracts found in Japan. These genes are supposedly involved in organogenesis and maintenance of transparency of the lens. According to the results of fine mapping of Rupture of lens cataract (RLC), we sequenced a number of the cDNA clones at the map positions obtained from the mouse full-length cDNA encyclopedia developed by RIKEN. One of cDNA clones, rlcl, was found to have deletion of 27 bp, when compared with the normal cDNA sequence. This deletion was specific to RLC mutant. Rabbit antiserum to the C-terminus peptide of rlcl product detected a 110 kDa polypeptide in the lens. Immunohistochemistry with this antiseum revealed unique distribution in lens epithelium, nervous system and other tissues. Mechanism of cataractgenesis is now under investigation. On the other hand, the same positional approach in Nakano cataract (NCT) demonstrated a 13 bp deletion in nctl cDNA. This deletion was conserved in NK11, an established cell line of lens epithelium provided from NEL Careful examination of the lenses in N2 cross to MSM revealed two distinct forms of lens opacity in respect to distribution of cloudiness and latent period. We could map two modifier loci determining the subtypes of NCT cataract on Chr. 3 and 10.
To further confirm that these deletions are indeed causative mutation, rescue with normal full size cDNA and targeting experiments are now in progress in this laboratory.
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Research Products
(12 results)
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[Publications] Tachibana, M., Adachi, W., Kinoshita, S., Kobayashi, K., Honma, Y., Hiai, H., Matsushima, Y.: "Androgen-dependent mouse keratoconus links to a MHC region including the sex-limited protein gene"Inv. Ophthal. Vis. Sci.. 43. 51-57 (2002)
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「研究成果報告書概要(欧文)」より
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[Publications] Tsuruyama, T., Nakamura, T., Jin, G., Ozeki, M, Yamada, Y., Hiai, H.: "Constitutive activation of Stat5a by retrovirus integration in early pre-B lymphomas of SL/Kh strain mice"Proc. Natl. Acd. Sci. USA. 99. 8253-8258 (2002)
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「研究成果報告書概要(欧文)」より
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[Publications] Narita, M., Wang, Y., Kita, A., Omi, N., Yamada, Y., Hiai, H.: "Genetic analysis of Nakano cataract and its modifier genes in mice"Exp. Eye Res.. 75. 745-751 (2002)
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[Publications] Kayahara, T., Sawada, M., Takaishi, S., Fukui, H., Seno, H, Fukuzawa, H., Suzuki, K., Hiai, H., Kageyama, R., Okano, H., Chiba, T.: "Candidate markers for stem and early progehitor cells, Musashi-1 and Hesl, are expressed in crypt base columnar cells of mouse small intestine"FEBS Lett.. 535. 131-135 (2003)
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「研究成果報告書概要(欧文)」より
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