DEAD-box helicase DDX27 regulates 3′ end formation of ribosomal 47S RNA and stably associates with the PeBoW-complex

• Published in: Experimental cell research Vol. 334; no. 1; pp. 146 - 159
• Main Authors: Kellner, Markus, Rohrmoser, Michaela, Forné, Ignasi, Voss, Kirsten, Burger, Kaspar, Mühl, Bastian, Gruber-Eber, Anita, Kremmer, Elisabeth, Imhof, Axel, Eick, Dirk
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.05.2015; Elsevier BV
• Subjects: 60 APPLIED LIFE SCIENCES; Cellular biology; DEAD-box helicase; DEAD-box RNA Helicases - metabolism; Enzymes; FASTENING; F×F motif; Humans; Mass spectrometry; MASS SPECTROSCOPY; MATURATION; Multiprotein Complexes - metabolism; Nuclear Proteins - metabolism; Nucleolus; PeBoW-complex; PROTEINS; Proteins - metabolism; Ribonucleic acid; RIBOSOMAL RNA; RNA; RNA, Ribosomal - metabolism; rRNA processing; SULFUR 28; SULFUR 47; Tumor Cells, Cultured; F×F motif; Nucleolus; PeBoW-complex; DEAD-box helicase; rRNA processing
• ISSN: 0014-4827; 1090-2422
• DOI: 10.1016/j.yexcr.2015.03.017

PeBoW, a trimeric complex consisting of pescadillo (Pes1), block of proliferation (Bop1), and the WD repeat protein 12 (WDR12), is essential for processing and maturation of mammalian 5.8S and 28S ribosomal RNAs. Applying a mass spectrometric analysis, we identified the DEAD-box helicase DDX27 as stably associated factor of the PeBoW-complex. DDX27 interacts with the PeBoW-complex via an evolutionary conserved F×F motif in the N-terminal domain and is recruited to the nucleolus via its basic C-terminal domain. This recruitment is RNA-dependent and occurs independently of the PeBoW-complex. Interestingly, knockdown of DDX27, but not of Pes1, induces the accumulation of an extended form of the primary 47S rRNA. We conclude that DDX27 can interact specifically with the Pes1 and Bop1 but fulfils critical function(s) for proper 3′ end formation of 47S rRNA independently of the PeBoW-complex. •DEAD-box helicase DDX27 is a new constituent of the PeBoW-complex.•The N-terminal F×F motif of DDX27 interacts with the PeBoW components Pes1 and Bop1.•Nucleolar anchoring of DDX27 via its basic C-terminal domain is RNA dependent.•Knockdown of DDX27 induces a specific defect in 3′ end formation of 47S rRNA.