Project/Area Number |
08680739
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Molecular biology
|
Research Institution | KYOTO UNIVERSITY |
Principal Investigator |
MESHI Tetsuo Kyoto University, Dept.Bot., Associate Professor, 大学院・理学研究科, 助教授 (40157813)
|
Co-Investigator(Kenkyū-buntansha) |
IWABUCHI Masaki Kyoto University, Dept.Bot., Professor, 大学院・理学研究科, 教授 (30000839)
|
Project Period (FY) |
1996 – 1997
|
Project Status |
Completed (Fiscal Year 1997)
|
Budget Amount *help |
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1997: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 1996: ¥1,000,000 (Direct Cost: ¥1,000,000)
|
Keywords | leghemoglobin / MAR / nuclear matrix / soybean / gene expression / ダイズ / メチル化 / 一本鎖解離領域 |
Research Abstract |
Nodules of leguminous plants contain infected and non-infected cells, which are discriminated in gene expression, ploidy, metabolism, morphology and so on. In this work, we focussed on leghemoglobin(Lb)genes which are expressed exclusively in infected cells, to lead a better understanding of gene regulation at the level of higher-order chromatin structure by comparing the state of the Lb locus between infected and non-infected cells. Followings were carried out and clarified. 1.We have isolated genomic clones covering two Lb loci. 2.We have established the method of the isolation of nuclei from nodules. 3.Most of the Lb loci have high affinity with the nuclear matrix. 4.A large number of BURs(base-unparing regions)were found in an Lb locus, consistent with the observation that it contained many MARs. 5.We have established the method by which protoplasts were isolated from infected and non-infected cells separately. 6.Methylation levels in the Lb loci was found to be rather low. 7.Sensitivity to DNase I is rather high around the Lbc3 gene irrespective of expression. Thus, we have obtained basic data concerning the chromatin structure of the Lb loci. Some findings are not necessarily consistent with previously reported results. Further investigation is necessary to clarify the relationship between gene expression and chromatin structure.
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