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Involvement multiple factors in p53-dependent gene regulation in response to low-dose radiation

https://repo.qst.go.jp/records/60551
https://repo.qst.go.jp/records/60551
94cf604a-25c8-412c-b8ee-33069307579b
Item type 会議発表用資料 / Presentation(1)
公開日 2004-09-14
タイトル
タイトル Involvement multiple factors in p53-dependent gene regulation in response to low-dose radiation
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 Nenoi, Mitsuru

× Nenoi, Mitsuru

WEKO 600821

Nenoi, Mitsuru

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Daino, Kazuhiro

× Daino, Kazuhiro

WEKO 600822

Daino, Kazuhiro

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Ichimura, Sachiko

× Ichimura, Sachiko

WEKO 600823

Ichimura, Sachiko

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根井 充

× 根井 充

WEKO 600824

en 根井 充

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臺野 和広

× 臺野 和広

WEKO 600825

en 臺野 和広

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沼田 幸子

× 沼田 幸子

WEKO 600826

en 沼田 幸子

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抄録
内容記述タイプ Abstract
内容記述 Elucidation of how living organisms respond to ionizing radiation of doses lower than 0.5Gy is critical for establishment of a scientifically-justified risk assessment. It has been revealed that low-dose radiation causes distinct biological responses, such as adaptive responses, bystander effects and induction of genomic instability, which were not observed in experiments using lethal dose of radiation. There is accumulating evidence showing that p53 plays a pivotal role in these low-dose radiation-distinct responses. In fact, p53 is activated by a faint damage of the genome, and its target genes, such as p21WAF1/CIP1, GADD45a and MDM2, are induced by low-dose radiation. We have observed 8-fold increase in p21 gene transcription and 5-fold increase in GADD45a gene transcription after 0.5Gy of X rays in human myeloblastic leukemia cell line ML1. However activation of p53 by radiation is not limited in a low-dose range. Therefore, as yet determined mechanisms involving p53 must be operating in inducing the low-dose radiation-distinct biological responses. In this regard, it is noteworthy that a lot of nuclear factors have been demonstrated to associate with p53, modulating its function in regulation of the downstream genes. For examples, transcription factors Sp1, gut-enriched kruppel-like factor (GKLF), Ets1, and interferon regulatory factor-1 (1RF-1) have been shown to be involved in the p53-dependent transcriptional activation. BRCA1 has also been shown to play a role in both p53-dependent and p53-independent transcriptional activation of the GADD45a gene. Histone acetyl transferase p300/CBP and PHD-finger motif proteins ING family are the cofactors, modulating p53 function through chromatin remodeling. Based on these observations, it may be hypothesized that a specific combination of cooperating transcription factors and cofactors is activated by low-dose radiation, and it causes a distinct biological response. We attempt here to review recent data, including ours, concerning nuclear factors participating in transcriptional regulation by p53
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 The Fifth Japan-France Workshop on Radiobiology and Medical Imaging
発表年月日
日付 2004-06-04
日付タイプ Issued
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