Publication | Open Access
Mechanism of the AAA+ ATPases pontin and reptin in the biogenesis of H/ACA RNPs
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Citations
44
References
2012
Year
Molecular RegulationMolecular BiologyRedox BiologyTranscriptional RegulationAaa+ Atpases PontinH/aca RnpsReptin FunctionCell SignalingProtein FunctionBiochemistryDna ReplicationCell BiologyProtein PhosphorylationProtein BiosynthesisChromatin FunctionTranscription RegulationChromatinSignal TransductionChromatin RemodelingNatural SciencesCellular BiochemistrySystems BiologyMedicineNap57 Domain
The AAA+ ATPases pontin and reptin function in a staggering array of cellular processes including chromatin remodeling, transcriptional regulation, DNA damage repair, and assembly of macromolecular complexes, such as RNA polymerase II and small nucleolar (sno) RNPs. However, the molecular mechanism for all of these AAA+ ATPase associated activities is unknown. Here we document that, during the biogenesis of H/ACA RNPs (including telomerase), the assembly factor SHQ1 holds the pseudouridine synthase NAP57/dyskerin in a viselike grip, and that pontin and reptin (as components of the R2TP complex) are required to pry NAP57 from SHQ1. Significantly, the NAP57 domain captured by SHQ1 harbors most mutations underlying X-linked dyskeratosis congenita (X-DC) implicating the interface between the two proteins as a target of this bone marrow failure syndrome. Homing in on the essential first steps of H/ACA RNP biogenesis, our findings provide the first insight into the mechanism of action of pontin and reptin in the assembly of macromolecular complexes.
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