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The human methyltransferase ZCCHC4 catalyses N-6-methyladenosine modification of 28S ribosomal RNA

机译:人甲基转移酶ZCCHC4催化剂N-6-甲基腺苷修饰28S核糖体RNA

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摘要

RNA methylations are essential both for RNA structure and function, and are introduced by a number of distinct methyltransferases (MTases). In recent years, N-6-methyladenosine (m(6)A) modification of eukaryotic mRNA has been subject to intense studies, and it has been demonstrated that m(6)A is a reversible modification that regulates several aspects of mRNA function. However, m(6)A is also found in other RNAs, such as mammalian 18S and 28S ribosomal RNAs (rRNAs), but the responsible MTases have remained elusive. 28S rRNA carries a single m(6)A modification, found at position A4220 (alternatively referred to as A4190) within a stem-loop structure, and here we show that the MTase ZCCHC4 is the enzyme responsible for introducing this modification. Accordingly, we found that ZCCHC4 localises to nucleoli, the site of ribosome assembly, and that proteins involved in RNA metabolism are overrepresented in the ZCCHC4 interactome. Interestingly, the absence of m(6)A4220 perturbs codon-specific translation dynamics and shifts gene expression at the translational level. In summary, we establish ZCCHC4 as the enzyme responsible for m(6)A modification of human 28S rRNA, and demonstrate its functional significance in mRNA translation.
机译:RNA甲基化对于RNA结构和功能既是必不可少的,并且由许多不同的甲基转移酶(MTases)引入。近年来,N-6-甲基腺苷(M(6)A)真核mRNA的改性已受到强烈的研究,并且已经证明了M(6)A是调节mRNA功能的几个方面的可逆修饰。然而,在其他RNA中也发现了M(6)A,例如哺乳动物18S和28S核糖体RNA(RRNA),但负责的MTases仍然难以捉摸。 28S RRNA携带单一M(6)的修饰,在茎环结构内以A4220(或者称为A4190)在茎环结构中发现,并且在此表明MTase ZCCHC4是负责引入该改性的酶。因此,我们发现ZCCHC4定位于核仁,核糖体组装部位,并且参与RNA代谢的蛋白质在ZCCHC4互联蛋白组中呈现出叠加。有趣的是,没有M(6)A4220 Perturbs Codon特异性翻译动态并在翻译水平转移基因表达。总之,我们建立ZCCHC4作为负责M(6)的酶的酶,对人28s RRNA的修饰,并证明其在MRNA翻译中的功能意义。

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  • 来源
    《Nucleic Acids Research》 |2020年第2期|共17页
  • 作者单位

    Univ Oslo Fac Math &

    Nat Sci Dept Biosci N-0316 Oslo Norway;

    Norwegian Univ Sci &

    Technol Dept Clin &

    Mol Med NTNU NO-7491 Trondheim Norway;

    Univ Copenhagen NNF Fac Hlth &

    Med Sci Prote Program CPR Blegdamsvej 3B DK-2200 Copenhagen Denmark;

    Max Planck Inst Mol Biomed Max Planck Res Grp RNA Biol D-48149 Munster Germany;

    Radboud Univ Nijmegen Fac Sci Radboud Inst Mol Life Sci Oncode Inst Dept Mol Biol NL-6500 HB Nijmegen Netherlands;

    Univ Toulouse Ctr Biol Integrat Lab Biol Mol Eucaryote UPS CNRS Toulouse France;

    Univ Copenhagen NNF Fac Hlth &

    Med Sci Prote Program CPR Blegdamsvej 3B DK-2200 Copenhagen Denmark;

    Univ Oslo Fac Math &

    Nat Sci Dept Biosci N-0316 Oslo Norway;

    Max Planck Inst Mol Biomed Max Planck Res Grp RNA Biol D-48149 Munster Germany;

    Univ Southern Denmark Dept Biochem &

    Mol Biol Campusvej 55 DK-5230 Odense M Denmark;

    Univ Copenhagen NNF Fac Hlth &

    Med Sci Prote Program CPR Blegdamsvej 3B DK-2200 Copenhagen Denmark;

    Univ Toulouse Ctr Biol Integrat Lab Biol Mol Eucaryote UPS CNRS Toulouse France;

    Radboud Univ Nijmegen Fac Sci Radboud Inst Mol Life Sci Oncode Inst Dept Mol Biol NL-6500 HB Nijmegen Netherlands;

    Max Planck Inst Mol Biomed Max Planck Res Grp RNA Biol D-48149 Munster Germany;

    Norwegian Univ Sci &

    Technol Dept Clin &

    Mol Med NTNU NO-7491 Trondheim Norway;

    Univ Oslo Fac Math &

    Nat Sci Dept Biosci N-0316 Oslo Norway;

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  • 正文语种 eng
  • 中图分类 生物化学;
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