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DENR-MCT-1 promotes translation re-initiation downstream of uORFs to control tissue growth

机译:DENR-MCT-1促进uORF下游的翻译重新初始化,以控制组织的生长

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摘要

During cap-dependent eukaryotic translation initiation, ribosomes scan messenger RNA from the 5' end to the first AUG start codon with favourable sequence context. For many mRNAs this AUG belongs to a short upstream open reading frame (uORF), and translation of the main downstream ORF requires re-initiation, an incompletely understood process. Re-initiation is thought to involve the same factors as standard initiation. It is unknown whether any factors specifically affect translation re-initiation without affecting standard cap-dependent translation. Here we uncover the non-canonical initiation factors density regulated protein (DENR) and multiple copies in T-cell lymphoma-1 (MCT-1; also called MCTS1 in humans) as the first selective regulators of eukaryotic re-initiation. mRNAs containing upstream ORFs with strong Kozak sequences selectively require DENR-MCT-1 for their proper translation, yielding a novel class of mRNAs that can be co-regulated and that is enriched for regulatory proteins such as oncogenic kinases. Collectively, our data reveal that cells have a previously unappreciated translational control system with a key role in supporting proliferation and tissue growth.
机译:在帽依赖的真核翻译起始过程中,核糖体从5'末端到第一个AUG起始密码子扫描信使RNA,并具有有利的序列背景。对于许多mRNA,此AUG属于较短的上游开放阅读框(uORF),主要下游ORF的翻译需要重新初始化,这是一个不完全了解的过程。重新启动被认为涉及与标准启动相同的因素。尚不清楚是否有任何因素在不影响标准上限相关翻译的情况下专门影响翻译重新初始化。在这里,我们发现非经典的起始因子密度调节蛋白(DENR)和T细胞淋巴瘤1(MCT-1;在人类中也称为MCTS1)中的多个拷贝,是真核生物重新启动的第一个选择性调节因子。包含具有强Kozak序列的上游ORF的mRNA有选择地需要DENR-MCT-1进行适当的翻译,从而产生一类新型的mRNA,这些mRNA可以被共同调控,并且富含调控蛋白,例如致癌激酶。总的来说,我们的数据表明细胞具有以前未受赞赏的翻译控制系统,在支持增殖和组织生长中起关键作用。

著录项

  • 来源
    《Nature》 |2014年第7513期|208-212|共5页
  • 作者单位

    German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany,Center for Molecular Neurobiology (ZMNH), University Medical Center Hamburg-Eppendorf (UKE), Falkenried 94, 20251 Hamburg, Germany;

    German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany;

    Center for Molecular Neurobiology (ZMNH), University Medical Center Hamburg-Eppendorf (UKE), Falkenried 94, 20251 Hamburg, Germany;

    Center for Molecular Neurobiology (ZMNH), University Medical Center Hamburg-Eppendorf (UKE), Falkenried 94, 20251 Hamburg, Germany;

    Center for Molecular Neurobiology (ZMNH), University Medical Center Hamburg-Eppendorf (UKE), Falkenried 94, 20251 Hamburg, Germany;

    German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany,Zentrum fuer Molekulare Biologie der Universitaet Heidelberg (ZMBH), DKFZ-ZMBH Alliance, 69120 Heidelberg, Germany;

    German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany;

    Center for Molecular Neurobiology (ZMNH), University Medical Center Hamburg-Eppendorf (UKE), Falkenried 94, 20251 Hamburg, Germany;

    German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany,Zentrum fuer Molekulare Biologie der Universitaet Heidelberg (ZMBH), DKFZ-ZMBH Alliance, 69120 Heidelberg, Germany;

    Center for Molecular Neurobiology (ZMNH), University Medical Center Hamburg-Eppendorf (UKE), Falkenried 94, 20251 Hamburg, Germany;

    German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 02:53:09

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