2001 Fiscal Year Final Research Report Summary
Functional analyses of ATF-2 gene family members by using knockout-mouse
Project/Area Number |
12670126
|
Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
General medical chemistry
|
Research Institution | The Institute of Physical and Chemical Research |
Principal Investigator |
MAEKAWA Toshio RIKEN, Molecular Genetics Laboratory, Senior Scientist, 分子遺伝学研究室, 副主任研究員 (90201764)
|
Project Period (FY) |
2000 – 2001
|
Keywords | Transcription factor / ATF-2 / Mammary tumour / GADD45 / APC / c-jun / Anisomycin / Knockoutmouse |
Research Abstract |
We have generated and anaiyzed the mutant mouse lacking transcription factor ATF-2 gene far members. 1.ATF-2 heterozygously knockout female mouse developed mammary tumours at very high ratio 18/ : Most of these tumours were adenocarcinoma scirrhus. 2, By using Tip-Technology, we have found that the expressions of APC and c-jun are reduced sev folds in ATF-2 deficient MEF. 3, We have found that the induction of GADD45 gene by anisomycin is inhibited in the ATF-2 defic cell line. 4, The expression levels of GADD45 gene were much reduced in the tumours than in normal mammal 5, ATF-2 homozygously and heterozygously knockout MEFs that express activated RAS develo tumours in nude-mouse at 100%, but wild type MEF that express activated RAS couldn't develop tumours. 6, From these results we can say that ATF-2 heterozygously knockout femaie mouse have high potent to develop tumours.
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Research Products
(4 results)