| Project/Area Number |
07044268
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| Research Category |
Grant-in-Aid for international Scientific Research
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| Allocation Type | Single-year Grants |
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| Section | Joint Research |
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| Research Institution | Okayama University Medical School |
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Principal Investigator |
NINOMIYA Yoshifumi Okayama University Medical School, 医学部, 教授 (70126241)
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| Co-Investigator(Kenkyū-buntansha) |
オウ スーク・ポール ハーバード大学, 医学部, 研究員
ウオルマン マット ハーバード大学, 医学部, 研究員
アプラ スニール ハーバード大学, 医学部, 研究員
MOMOTA Ryusuke Okayama University Medical School, 医学部, 助手 (80263557)
OOHASHI Toshitaka Okayama University Medical School, 医学部, 助手 (50194262)
オルセン ビヨン ハーバード大学, 医学部, 教授
APTA Suneel Harvard Medical School
OLSEN Bjorn Harvard Medical School
OH Suk Paul Harvard Medical School
WARMAN Matt Harvard Medical School
スーク ポール・オウ ハーバード大学, 医学部, 研究員
マット ウォルマン ハーバード大学, 医学部, 研究員
スニール アプラ ハーバード大学, 医学部, 研究員
ビヨン オルセン ハーバード大学, 医学部, 教授
マット ウオルマン ハーバード大学, 医学部, 研究員
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| Project Period (FY) |
1995 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥4,000,000 (Direct Cost: ¥4,000,000)
Fiscal Year 1996: ¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1995: ¥2,000,000 (Direct Cost: ¥2,000,000)
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| Keywords | genomic library / monoclonal antibodies / homologous recombination / collagen genes / phynotypic change / knockout mouse / 遺伝子ライブラリ / cDNAライブラリー / IV型コラーゲン |
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| Research Abstract |
1) We have cloned many overlapping cDNAs coding for the mouse alpha6 (IV) collagen chain and determined primary structure of the alpha6 (IV) chain polypeptide.
2) We raised monoclonal antibodies against amino acid sequences from various parts of the mouse alpha6 (IV) collagen polypeptide chain and used them for the tissue distribution. The results indicated that the tissue distribution for the chain was similar to that of the human alpha6 (IV) collagen chain. Interestingly, the distribution of the paired genes ; col4a1/col4a2, col4a3/col4a4, and col4a5/col4a6 is quite synchronous except for the glomerular basement membranes.
3) We have some indication that shows alternative splicing in exon 31. Currently, we are characterizing this atypical splicing event in terms of tissue specific expression.
4) In order to create a knockout mice for col4a6, we made several constructs including the one where the exon 2 was taken out and the foreign gene, Neo^R gene was inserted instead. The construct was transfected into Stem cells by homologous recombination. Currently, we are characterizing knockout mice to detect any phenotypic changes in heterozygotes and homozygotes.
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