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  1. 原著論文

Radiation-induced deletions in the 5' end region of Notch1 lead to the formation of truncated proteins and are involved in the development of mouse thymic lymphomas

https://repo.qst.go.jp/records/44525
https://repo.qst.go.jp/records/44525
ce61f765-6a35-4982-a57b-0445b88817f2
Item type 学術雑誌論文 / Journal Article(1)
公開日 2006-08-03
タイトル
タイトル Radiation-induced deletions in the 5' end region of Notch1 lead to the formation of truncated proteins and are involved in the development of mouse thymic lymphomas
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_6501
資源タイプ journal article
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 Tsuji, Hideo

× Tsuji, Hideo

WEKO 442425

Tsuji, Hideo

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Ishii-Ohba, Hiroko

× Ishii-Ohba, Hiroko

WEKO 442426

Ishii-Ohba, Hiroko

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Ukai, Hideki

× Ukai, Hideki

WEKO 442427

Ukai, Hideki

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Katsube, Takanori

× Katsube, Takanori

WEKO 442428

Katsube, Takanori

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Ogiu, Toshiaki

× Ogiu, Toshiaki

WEKO 442429

Ogiu, Toshiaki

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辻 秀雄

× 辻 秀雄

WEKO 442430

en 辻 秀雄

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石井 洋子

× 石井 洋子

WEKO 442431

en 石井 洋子

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鵜飼 英樹

× 鵜飼 英樹

WEKO 442432

en 鵜飼 英樹

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勝部 孝則

× 勝部 孝則

WEKO 442433

en 勝部 孝則

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荻生 俊昭

× 荻生 俊昭

WEKO 442434

en 荻生 俊昭

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抄録
内容記述タイプ Abstract
内容記述 Notch1 protein is a transmembrane receptor that directs various cell fate decisions. Active forms of Notch1 consisting of a transmembrane domain and an intracellular domain (Notch1TM) or only an intracellular domain (Notch1IC) function as oncoproteins. To elucidate the effect of Notch1 abnormalities in radiation-induced lymphomagenesis, we determined the structure of the Notch1 gene and examined the frequency and the sites of Notch1 rearrangements in radiation-induced mouse thymic lymphomas. The Notch1 gene consists of 37 exons, including three exons upstream of the previously reported exon 1. The transcript starting from exon 1 was the major transcript whereas the transcripts read upstream from exon 1a, in which amino acid sequences in the N-terminal region were changed, were minor. More than 50% of radiation-induced thymic lymphomas exhibited Notch1 rearrangements, suggesting that Notch1 acts as a major oncogene in radiation-induced lymphomagenesis. We identified three rearranged sites: novel sites in the 5' end region encompassing exons 1 and 2, the previously identified juxtamembrane extracellular region, and the 3' end region. The 5' deletion and the insertion of murine leukemia virus in the juxtamembrane region led to the production of abnormal transcripts starting from cryptic transcription start sites located halfway through the Notch1 gene and resulted in transcripts lacking most of the extracellular domain. As a result of these rearrangements, truncated Notch1 polypeptides resembling Notch1TM or Notch1IC were formed. In contrast, the 3' deletion led to the production of a C-terminal PEST motif-deleted transcript. The downstream target gene Hes1 was transcribed in a lymphoma with insertion of murine leukemia virus, but not in a lymphoma with a 5' deletion. These results indicate that in addition to Hes1 expression, other Notch1 pathway(s) have a role in thymic lymphomagenesis and suggest the presence of a novel mechanism for oncogenic activation of Notch1 by 5' deletion.
書誌情報 Carcinogenesis

巻 24, p. 1257-1268, 発行日 2003
ISSN
収録物識別子タイプ ISSN
収録物識別子 0143-3334
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