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Archaeal fibrillarin-Nop5 heterodimer 2'-O-methylates RNA independently of the C/D guide RNP particle.


ABSTRACT: Archaeal fibrillarin (aFib) is a well-characterized S-adenosyl methionine (SAM)-dependent RNA 2'-O-methyltransferase that is known to act in a large C/D ribonucleoprotein (RNP) complex together with Nop5 and L7Ae proteins and a box C/D guide RNA. In the reaction, the guide RNA serves to direct the methylation reaction to a specific site in tRNA or rRNA by sequence complementarity. Here we show that a Pyrococcus abyssi aFib-Nop5 heterodimer can alone perform SAM-dependent 2'-O-methylation of 16S and 23S ribosomal RNAs in vitro independently of L7Ae and C/D guide RNAs. Using tritium-labeling, mass spectrometry, and reverse transcription analysis, we identified three in vitro 2'-O-methylated positions in the 16S rRNA of P. abyssi, positions lying outside of previously reported pyrococcal C/D RNP methylation sites. This newly discovered stand-alone activity of aFib-Nop5 may provide an example of an ancestral activity retained in enzymes that were recruited to larger complexes during evolution.

SUBMITTER: Tomkuviene M 

PROVIDER: S-EPMC5558902 | biostudies-literature | 2017 Sep

REPOSITORIES: biostudies-literature

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Archaeal fibrillarin-Nop5 heterodimer 2'-<i>O</i>-methylates RNA independently of the C/D guide RNP particle.

Tomkuvienė Miglė M   Ličytė Janina J   Olendraitė Ingrida I   Liutkevičiūtė Zita Z   Clouet-d'Orval Béatrice B   Klimašauskas Saulius S  

RNA (New York, N.Y.) 20170602 9


Archaeal fibrillarin (aFib) is a well-characterized <i>S</i>-adenosyl methionine (SAM)-dependent RNA 2'-<i>O</i>-methyltransferase that is known to act in a large C/D ribonucleoprotein (RNP) complex together with Nop5 and L7Ae proteins and a box C/D guide RNA. In the reaction, the guide RNA serves to direct the methylation reaction to a specific site in tRNA or rRNA by sequence complementarity. Here we show that a <i>Pyrococcus abyssi</i> aFib-Nop5 heterodimer can alone perform SAM-dependent 2'-  ...[more]

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