| Project/Area Number |
08556047
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 展開研究 |
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| Research Field |
Basic veterinary science/Basic zootechnical science
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| Research Institution | The University of Tokyo |
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Principal Investigator |
SHIOTA Kunio The University of Tokyo, Graduate School of Agricultural and Life Sciences, Professor, 大学院・農学生命科学研究科, 教授 (80196352)
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| Co-Investigator(Kenkyū-buntansha) |
AONO Fumihito Kyoudoushiryou Co., Resercher, 研究所, 研究員
GOIZUKA Ryou Science University of Tokyo, Research Institute for Biological Science, Associat, 生命科学研究所, 助教授 (60205581)
OGAWA Hiroyuki The University of Tokyo, Graduate School of Agricultural and Life Sciences, Prof, 大学院・農学生命科学研究科, 教授 (30012016)
SASAKI Nobuo The University of Tokyo, Graduate School of Agricultural and Life Sciences, Prof, 大学院・農学生命科学研究科, 教授 (60107414)
MIYAKE Youichi Iwate University, Department of Veterinary Medicine, Associate Professor, 農学部, 助教授 (20002256)
小川 智也 東京大学, 大学院・農学生命科学研究科, 教授 (30087572)
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| Project Period (FY) |
1996 – 1998
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| Project Status |
Completed (Fiscal Year 1998)
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| Budget Amount *help |
¥14,600,000 (Direct Cost: ¥14,600,000)
Fiscal Year 1998: ¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 1997: ¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 1996: ¥8,400,000 (Direct Cost: ¥8,400,000)
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| Keywords | CpG islands / Genomic scanning / Genetic disorders / Tissue-specifically demethylation / DNA methyltransferase / 形態形成 / FISH法 / イソ染色体構造 / ゲノムメチル化 / RLGS法 / 形質遺伝子 |
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| Research Abstract |
Recent advance in the artificial insemination technique by using frozen-preserved semen greatly enhanced a production of economically superior livestock animals. It, however, ironically helped cryptic genetic disorders to spread world wide in an unexpected speed. Thus, it has been needed to establish effective way of genome-wide screening for genetic abnormalities in livestock animals. To this end, it was aimed to develop a system to identify changes in a structure of genomic DNA by a restriction landmark genomic scanning (RLGS) method. In the RLGS, genomic DNA is digested by two or more different kind of restriction enzymes, and separated by the 2-dimensional gel electrophoresis (2D/E). It is, therefore, possible to sensitively identify global genomic changes such as point mutations at the recognition sites of restriction enzymes, deletions, translocations, etc. RLGS should be also useful to establish a linkages between a certain valuable phenotype and a set of multiple genes.
In this study, we analyzed CpG islands of rat genomic DNA by RLGS using NotI, a methylation sensitive enzyme. As a result, we found approximately 1% of the "RLGS spots" show tissue-specific distribution, suggesting that these spots are tissue-specifically methylated/demethylated. Of these spots, we could subsequently clone several genomic fragments which appeared to be demerhylated in placenta but not in kidney. Sequence analysis of isolated clones revealed that one of the clones encodes mitochondrial C3 transporter gene which appeared to be relatively highly expressed in the placenta but low in kidney in further analysis. These results showed that the RLGS is an effective way of identification and isolation of genomic DNA fragments by genome-wide scanning for the genetic changes.
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