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  1. 医学
  2. 発表論文(医学系)

Translational Repression of a Splice Variant of Cynomolgus Macaque CXCL1L by Its C-terminal Sequence

http://hdl.handle.net/2298/39222
http://hdl.handle.net/2298/39222
1d10cf14-8974-4b33-817b-eee73d360d3a
名前 / ファイル ライセンス アクション
Nomiyama_et_al(JICR).pdf Nomiyama_et_al(JICR).pdf (2.5 MB)
Item type プレプリント / Preprint(1)
公開日 2018-03-07
タイトル
タイトル Translational Repression of a Splice Variant of Cynomolgus Macaque CXCL1L by Its C-terminal Sequence
言語
言語 eng
キーワード
主題 chemokine, CXCL1L, translational regulation, gene duplication, evolution, cynomolgus macaque, Old World monkeys, ケモカイン, 翻訳制御, 遺伝子重複, 進化, カニクイザル, 旧世界ザル
資源タイプ
資源タイプ other
著者 Nomiyama, Hisayuki

× Nomiyama, Hisayuki

WEKO 136289

Nomiyama, Hisayuki

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Osada, Naoki

× Osada, Naoki

WEKO 136290

Osada, Naoki

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Takahashi, Ichiro

× Takahashi, Ichiro

WEKO 136291

Takahashi, Ichiro

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Terao, Keiji

× Terao, Keiji

WEKO 136292

Terao, Keiji

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Yamagata, Kazuya

× Yamagata, Kazuya

WEKO 136293

Yamagata, Kazuya

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Yoshie, Osamu

× Yoshie, Osamu

WEKO 136294

Yoshie, Osamu

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別言語の著者 野見山, 尚之

× 野見山, 尚之

WEKO 136301

野見山, 尚之

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長田, 直樹

× 長田, 直樹

WEKO 136302

長田, 直樹

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高橋, 一郎

× 高橋, 一郎

WEKO 136303

高橋, 一郎

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寺尾, 恵治

× 寺尾, 恵治

WEKO 136304

寺尾, 恵治

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山縣, 和也

× 山縣, 和也

WEKO 136305

山縣, 和也

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義江, 修

× 義江, 修

WEKO 136306

義江, 修

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内容記述
内容記述 We previously isolated a cDNA clone from cynomolgus macaque encoding a novel CXC chemokine that we termed CXCL1L from its close similarity to CXCL1. However, the cDNA consisted of three exons instead of four exons typically seen in other CXC chemokines. Here we isolated a cDNA encoding the full length variant of CXCL1L that we term CXCL1Lβ. CXCL1Lβ is 50 amino acids longer than the original CXCL1L, which we now term CXCL1Lα. The CXCL1Lβ mRNA is much more abundantly expressed in the cynomolgus macaque tissues than CXCL1Lα mRNA. However, CXCL1Lβ protein was poorly produced by transfected cells compared with that of CXCL1Lα. When the coding region of the 4th exon was fused to the C-terminus of CXCL1 or even to a non-secretory protein firefly luciferase, the fused proteins were also barely produced although the mRNAs were abundantly expressed. The polysome profiling analysis suggested that the inhibition was mainly at the translational level. Furthermore, we demonstrated the C-terminal five amino acids of CXCL1Lβ were critical for the translational repression. The present study thus reveals a unique translational regulation controlling the production of a splicing variant of CXCL1L. Since the CXCL1L gene is functional only in the Old World monkeys, we also discuss possible reasons for the conservation of the active CXCL1L gene in these monkeys during the primate evolution.
書誌情報 Journal of Interferon & Cytokine Research

巻 37, 号 3, p. 129-138, 発行日 2017-03-17
ISSN
収録物識別子 10799907
DOI
関連タイプ isVersionOf
関連識別子 https://doi.org/10.1089/jir.2016.0085
フォーマット
内容記述タイプ Other
内容記述 application/pdf
形態
2488149 bytes
著者版フラグ
出版タイプ AO
出版タイプResource http://purl.org/coar/version/c_b1a7d7d4d402bcce
出版者
出版者 Mary Ann Liebert
資源タイプ・ローカル
プレプリント
資源タイプ・NII
Preprint
資源タイプ・DCMI
text
資源タイプ・ローカル表示コード
01
URL
内容記述タイプ Other
内容記述 https://www.liebertpub.com/doi/10.1089/jir.2016.0085
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