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  1. 原著論文

Retrotransposons Influence the Mouse Transcriptome: Implication for the Divergence of Genetic Traits

https://repo.qst.go.jp/records/45066
https://repo.qst.go.jp/records/45066
336ae84c-3aba-4aee-8d2e-3cd3d3b40c60
Item type 学術雑誌論文 / Journal Article(1)
公開日 2008-01-07
タイトル
タイトル Retrotransposons Influence the Mouse Transcriptome: Implication for the Divergence of Genetic Traits
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 Horie, Kyoji

× Horie, Kyoji

WEKO 447508

Horie, Kyoji

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Saito, Eisuke

× Saito, Eisuke

WEKO 447509

Saito, Eisuke

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W., Keng Vincent

× W., Keng Vincent

WEKO 447510

W., Keng Vincent

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Ikeda, Ryuji

× Ikeda, Ryuji

WEKO 447511

Ikeda, Ryuji

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Ishihara, Hiroshi

× Ishihara, Hiroshi

WEKO 447512

Ishihara, Hiroshi

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Takeda, Junji

× Takeda, Junji

WEKO 447513

Takeda, Junji

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石原 弘

× 石原 弘

WEKO 447514

en 石原 弘

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抄録
内容記述タイプ Abstract
内容記述 Massive accumulation of retrotransposons, comprising >40% of human and mouse genomes, is one of the major events in the evolution of the genome. However, most retrotransposons have lost retrotransposition competency, which makes studying their role in genome evolution elusive. Intracisternal A-particle (IAP) elements are long terminal repeat (LTR)-type mouse retrotransposons consisting of full-length and internally deleted types. Some are retrotransposition competent and their upregulated activity has been reported in mutant mice deficient in genome defense systems, suggesting that IAP elements provide a unique platform for studying the interaction between retrotransposons and mammalian genomes. Using the IAP element as a model case, here we show that mobilization of retrotransposons alters the mouse transcriptome. Retrotransposition assay in cultured cells demonstrated that a subset of internally deleted IAP elements, called IDelta1 type, retrotranspose efficiently when supplied with functional IAP proteins. Furthermore, the IDelta1 type IAP element exhibited substantial transcription-inducing activity in the flanking region. Genomewide transcript analysis of embryonic stem (ES) cells identified IAP-induced transcripts, including fusion transcripts between IAP sequence and endogenous genes. Unexpectedly, nearly half of these IAP elements obtained from ES cells derived from 129 mouse strain were absent in the C57BL/6 genome, suggesting that IAP-driven transcription contributes to the unique trait of the individual mouse strain. On the basis of these data, we propose that retrotransposons are one of the drivers that shape the mammalian transcriptome.
書誌情報 Genetics

巻 176, 号 2, p. 815-827, 発行日 2007-06
ISSN
収録物識別子タイプ ISSN
収録物識別子 0016-6731
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