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Degradation of nanoRNA is performed by multiple redundant RNases in Bacillus subtilis

Identifieur interne : 000168 ( France/Analysis ); précédent : 000167; suivant : 000169

Degradation of nanoRNA is performed by multiple redundant RNases in Bacillus subtilis

Auteurs : Ming Fang ; Wencke-Maria Zeisberg ; Ciaran Condon [France] ; Vasily Ogryzko [France] ; Antoine Danchin ; Undine Mechold

Source :

RBID : PMC:2731908

Descripteurs français

English descriptors

Abstract

Escherichia coli possesses only one essential oligoribonuclease (Orn), an enzyme that can degrade oligoribonucleotides of five residues and shorter in length (nanoRNA). Firmicutes including Bacillus subtilis do not have an Orn homolog. We had previously identified YtqI (NrnA) as functional analog of Orn in B. subtilis. Screening a genomic library from B. subtilis for genes that can complement a conditional orn mutant, we identify here YngD (NrnB) as a second nanoRNase in B. subtilis. Like NrnA, NrnB is a member of the DHH/DHHA1 protein family of phosphoesterases. NrnB degrades nanoRNA 5-mers in vitro similarily to Orn. Low expression levels of NrnB are sufficient for orn complementation. YhaM, a known RNase present in B. subtilis, degrades nanoRNA efficiently in vitro but requires high levels of expression for only partial complementation of the orn strain. A triple mutant (nrnA, nrnB, yhaM) in B. subtilis is viable and shows almost no impairment in growth. Lastly, RNase J1 seems also to have some 5′-to-3′ exoribonuclease activity on nanoRNA and thus can potentially finish degradation of RNA. We conclude that, unlike in E. coli, degradation of nanoRNA is performed in a redundant fashion in B. subtilis.


Url:
DOI: 10.1093/nar/gkp527
PubMed: 19553197
PubMed Central: 2731908


Affiliations:


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PMC:2731908

Le document en format XML

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<term>DNA (metabolism)</term>
<term>Genetic Complementation Test</term>
<term>Mutation</term>
<term>Oligoribonucleotides (chemistry)</term>
<term>Oligoribonucleotides (metabolism)</term>
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<term>Bacillus subtilis (enzymologie)</term>
<term>Bacillus subtilis (génétique)</term>
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<term>Ribonucléases (génétique)</term>
<term>Ribonucléases (métabolisme)</term>
<term>Test de complémentation</term>
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<term>Oligoribonucleotides</term>
<term>RNA</term>
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<term>Ribonucleases</term>
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<term>Ribonucleases</term>
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<term>DNA</term>
<term>Oligoribonucleotides</term>
<term>RNA</term>
<term>Ribonucleases</term>
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<term>Bacillus subtilis</term>
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<term>Bacillus subtilis</term>
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<term>Bacillus subtilis</term>
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<p>
<italic>Escherichia coli</italic>
possesses only one essential oligoribonuclease (Orn), an enzyme that can degrade oligoribonucleotides of five residues and shorter in length (nanoRNA). Firmicutes including
<italic>Bacillus subtilis</italic>
do not have an Orn homolog. We had previously identified YtqI (NrnA) as functional analog of Orn in
<italic>B. subtilis</italic>
. Screening a genomic library from
<italic>B. subtilis</italic>
for genes that can complement a conditional
<italic>orn</italic>
mutant, we identify here YngD (NrnB) as a second nanoRNase in
<italic>B. subtilis</italic>
. Like NrnA, NrnB is a member of the DHH/DHHA1 protein family of phosphoesterases. NrnB degrades nanoRNA 5-mers
<italic>in vitro</italic>
similarily to Orn. Low expression levels of NrnB are sufficient for
<italic>orn</italic>
complementation. YhaM, a known RNase present in
<italic>B. subtilis</italic>
, degrades nanoRNA efficiently
<italic>in vitro</italic>
but requires high levels of expression for only partial complementation of the
<italic>orn
<sup></sup>
</italic>
strain. A triple mutant (
<italic>nrnA</italic>
<sup></sup>
,
<italic>nrnB</italic>
<sup></sup>
,
<italic>yhaM</italic>
<sup></sup>
) in
<italic>B. subtilis</italic>
is viable and shows almost no impairment in growth. Lastly, RNase J1 seems also to have some 5′-to-3′ exoribonuclease activity on nanoRNA and thus can potentially finish degradation of RNA. We conclude that, unlike in
<italic>E. coli</italic>
, degradation of nanoRNA is performed in a redundant fashion in
<italic>B. subtilis</italic>
.</p>
</div>
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<affiliations>
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<li>France</li>
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<li>Île-de-France</li>
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<li>Paris</li>
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<name sortKey="Fang, Ming" sort="Fang, Ming" uniqKey="Fang M" first="Ming" last="Fang">Ming Fang</name>
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</record>

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