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Differentially expressed transcripts in Ikaros-defective lymphomas in irradiated B6C3F1 mice

https://repo.qst.go.jp/records/67451
https://repo.qst.go.jp/records/67451
9af6cb6a-ed5c-42a4-a598-c6c78683b7fb
Item type 会議発表用資料 / Presentation(1)
公開日 2003-09-01
タイトル
タイトル Differentially expressed transcripts in Ikaros-defective lymphomas in irradiated B6C3F1 mice
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Yasumura, Kyoko

× Yasumura, Kyoko

WEKO 663030

Yasumura, Kyoko

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Sugimura, Isamu

× Sugimura, Isamu

WEKO 663031

Sugimura, Isamu

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Kakinuma, Shizuko

× Kakinuma, Shizuko

WEKO 663032

Kakinuma, Shizuko

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Igarashi, Kazuei

× Igarashi, Kazuei

WEKO 663033

Igarashi, Kazuei

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Shimada, Yoshiya

× Shimada, Yoshiya

WEKO 663034

Shimada, Yoshiya

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安村 今日子

× 安村 今日子

WEKO 663035

en 安村 今日子

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柿沼 志津子

× 柿沼 志津子

WEKO 663036

en 柿沼 志津子

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島田 義也

× 島田 義也

WEKO 663037

en 島田 義也

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抄録
内容記述タイプ Abstract
内容記述 Ikaros, a Kruppel type zinc finger protein, is essential for the normal lymphocyte development and differentiation. We have previously shown that Ikaros was frequently altered in radiation-induced T-cell lymphomas and assumed that Ikaros inactivation might have deep connection with developing leukemia. Although inactivation of Ikaros is inferred to be involved in leukemogenesis, little is known about the molecular mechanisms leading to neoplastic transformation. In order to identify the potential genes under the control of Ikaros, we performed differential display on RNAs from 3T3-L1 cells transfected with or without Ikaros. Finally, two cDNA, TRK-fused gene (Tfg) and death-associated protein 3 (Dap3), which were up-regulated by Ikaros, were identified. On the contrary, the expression status of Tfg and Dap3 in radiation-induced T-cell lymphomas, which had defect in Ikaros expression, was to be significantly decreased. Furthermore, we found that upstream the transcription start site of Tfg and Dap3 contain putative binding sites of Ikaros. These results suggest that Tfg and Dap3 are the candidates downstream of Ikaros, which are possibly involved in radiation-induced lymphomagenesis.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 12th International Congress of Radiation Research
発表年月日
日付 2003-08-22
日付タイプ Issued
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