RBM7 subunit of the NEXT complex binds U-rich sequences and targets 3′-end extended forms of snRNAs

The Nuclear Exosome Targeting (NEXT) complex is a key cofactor of the mammalian nuclear exosome in the removal of Promoter Upstream Transcripts (PROMPTs) and potentially aberrant forms of other noncoding RNAs, such as snRNAs. NEXT is composed of three subunits SKIV2L2, ZCCHC8 and RBM7. We have recently identified the NEXT complex in our screen for oligo(U) RNA-binding factors. Here, we demonstrate that NEXT displays preference for U-rich pyrimidine sequences and this RNA binding is mediated by the RNA recognition motif (RRM) of the RBM7 subunit. We solved the structure of RBM7 RRM and identified two phenylalanine residues that are critical for interaction with RNA. Furthermore, we showed that these residues are required for the NEXT interaction with snRNAs in vivo. Finally, we show that depletion of components of the NEXT complex alone or together with exosome nucleases resulted in the accumulation of mature as well as extended forms of snRNAs. Thus, our data suggest a new scenario in which the NEXT complex is involved in the surveillance of snRNAs and/or biogenesis of snRNPs.

[1]  P. Cramer,et al.  Molecular Basis for Coordinating Transcription Termination with Noncoding RNA Degradation , 2014, Molecular cell.

[2]  Daniel R. Zerbino,et al.  Ensembl 2014 , 2013, Nucleic Acids Res..

[3]  Š. Vaňáčová,et al.  Mammalian DIS3L2 exoribonuclease targets the uridylated precursors of let-7 miRNAs , 2013, RNA.

[4]  A. Hyman,et al.  The human cap-binding complex is functionally connected to the nuclear RNA exosome , 2013, Nature Structural &Molecular Biology.

[5]  T. Jensen,et al.  CBC–ARS2 stimulates 3′-end maturation of multiple RNA families and favors cap-proximal processing , 2013, Nature Structural &Molecular Biology.

[6]  K. Stejskal,et al.  Suppression of peptide sample losses in autosampler vials. , 2013, Journal of proteome research.

[7]  F. Allain,et al.  RRM-RNA recognition: NMR or crystallography…and new findings. , 2013, Current opinion in structural biology.

[8]  R. Stefl,et al.  In vivo SELEX reveals novel sequence and structural determinants of Nrd1‐Nab3‐Sen1‐dependent transcription termination , 2012, The EMBO journal.

[9]  J. Steitz,et al.  Tri-snRNP-associated proteins interact with subunits of the TRAMP and nuclear exosome complexes, linking RNA decay and pre-mRNA splicing , 2012, RNA biology.

[10]  Michael T. McManus,et al.  Widespread RNA 3'-end oligouridylation in mammals. , 2012, RNA.

[11]  Š. Vaňáčová,et al.  Air2p is critical for the assembly and RNA-binding of the TRAMP complex and the KOW domain of Mtr4p is crucial for exosome activation , 2012, Nucleic acids research.

[12]  D. Fessas,et al.  Structural basis for dimethylarginine recognition by the Tudor domains of human SMN and SPF30 proteins , 2011, Nature Structural &Molecular Biology.

[13]  T. Jensen,et al.  Interaction profiling identifies the human nuclear exosome targeting complex. , 2011, Molecular cell.

[14]  Michael Sattler,et al.  Multi-domain conformational selection underlies pre-mRNA splicing regulation by U2AF , 2011, Nature.

[15]  J. Glicken,et al.  The PR/SET domain in PRDM4 is preceded by a zinc knuckle , 2011, Proteins.

[16]  A. Sandelin,et al.  PROMoter uPstream Transcripts share characteristics with mRNAs and are produced upstream of all three major types of mammalian promoters , 2011, Nucleic acids research.

[17]  Matthias Mann,et al.  High recovery FASP applied to the proteomic analysis of microdissected formalin fixed paraffin embedded cancer tissues retrieves known colon cancer markers. , 2011, Journal of proteome research.

[18]  G. M. Wilson,et al.  Different modes of interaction by TIAR and HuR with target RNA and DNA , 2011, Nucleic acids research.

[19]  G. M. Wilson,et al.  Unique properties of the Mtr4p-poly(A) complex suggest a role in substrate targeting. , 2010, Biochemistry.

[20]  Karel Kubicek,et al.  Recognition of Transcription Termination Signal by the Nuclear Polyadenylated RNA-binding (NAB) 3 Protein , 2010, The Journal of Biological Chemistry.

[21]  Mikkel H. Schierup,et al.  RNA Exosome Depletion Reveals Transcription Upstream of Active Human Promoters , 2008, Science.

[22]  Howard L McLeod,et al.  CANDID: a flexible method for prioritizing candidate genes for complex human traits , 2008, Genetic epidemiology.

[23]  S. Buratowski,et al.  The Nrd1–Nab3–Sen1 termination complex interacts with the Ser5-phosphorylated RNA polymerase II C-terminal domain , 2008, Nature Structural &Molecular Biology.

[24]  Morgan C. Giddings,et al.  High-Throughput SHAPE Analysis Reveals Structures in HIV-1 Genomic RNA Strongly Conserved across Distinct Biological States , 2008, PLoS biology.

[25]  D. Libri,et al.  Transcription termination and nuclear degradation of cryptic unstable transcripts: a role for the nrd1-nab3 pathway in genome surveillance. , 2006, Molecular cell.

[26]  J. Corden,et al.  Termination of cryptic unstable transcripts is directed by yeast RNA-binding proteins Nrd1 and Nab3. , 2006, Molecular cell.

[27]  Michael R Green,et al.  Structural basis for polypyrimidine tract recognition by the essential pre-mRNA splicing factor U2AF65. , 2006, Molecular cell.

[28]  S. Buratowski,et al.  Nrd1 interacts with the nuclear exosome for 3' processing of RNA polymerase II transcripts. , 2006, Molecular cell.

[29]  M. Gorenstein,et al.  Absolute Quantification of Proteins by LCMSE , 2006, Molecular & Cellular Proteomics.

[30]  B. Clurman,et al.  Zcchc8 is a glycogen synthase kinase-3 substrate that interacts with RNA-binding proteins. , 2005, Biochemical and biophysical research communications.

[31]  D. Black,et al.  Structure of PTB Bound to RNA: Specific Binding and Implications for Splicing Regulation , 2005, Science.

[32]  E. Petfalski,et al.  RNA Degradation by the Exosome Is Promoted by a Nuclear Polyadenylation Complex , 2005, Cell.

[33]  B. Séraphin,et al.  Cryptic Pol II Transcripts Are Degraded by a Nuclear Quality Control Pathway Involving a New Poly(A) Polymerase , 2005, Cell.

[34]  C. Dominguez,et al.  The RNA recognition motif, a plastic RNA‐binding platform to regulate post‐transcriptional gene expression , 2005, The FEBS journal.

[35]  W. Keller,et al.  A New Yeast Poly(A) Polymerase Complex Involved in RNA Quality Control , 2005, PLoS biology.

[36]  R. Stefl,et al.  RNA sequence‐ and shape‐dependent recognition by proteins in the ribonucleoprotein particle , 2005, EMBO reports.

[37]  L. Boros,et al.  Spermatogenetic expression of RNA-binding motif protein 7, a protein that interacts with splicing factors. , 2003, Journal of andrology.

[38]  M. Mann,et al.  Large-scale Proteomic Analysis of the Human Spliceosome References , 2006 .

[39]  D. Brow,et al.  RNA-binding protein Nrd1 directs poly(A)-independent 3′-end formation of RNA polymerase II transcripts , 2001, Nature.

[40]  S. Curry,et al.  Structure of tandem RNA recognition motifs from polypyrimidine tract binding protein reveals novel features of the RRM fold , 2000, The EMBO journal.

[41]  M. Swanson,et al.  A yeast heterogeneous nuclear ribonucleoprotein complex associated with RNA polymerase II. , 2000, Genetics.

[42]  P. Sharp,et al.  PUF60: a novel U2AF65-related splicing activity. , 1999, RNA.

[43]  M. Wilm,et al.  A doughnut‐shaped heteromer of human Sm‐like proteins binds to the 3′‐end of U6 snRNA, thereby facilitating U4/U6 duplex formation in vitro , 1999, The EMBO journal.

[44]  P. Mitchell,et al.  Functions of the exosome in rRNA, snoRNA and snRNA synthesis , 1999, The EMBO journal.

[45]  Kazuki Kurimoto,et al.  Structural basis for recognition of the tra mRNA precursor by the Sex-lethal protein , 1999, Nature.

[46]  M. Mann,et al.  The Exosome: A Conserved Eukaryotic RNA Processing Complex Containing Multiple 3′→5′ Exoribonucleases , 1997, Cell.

[47]  J. Thornton,et al.  AQUA and PROCHECK-NMR: Programs for checking the quality of protein structures solved by NMR , 1996, Journal of biomolecular NMR.

[48]  P. Kollman,et al.  A Second Generation Force Field for the Simulation of Proteins, Nucleic Acids, and Organic Molecules , 1995 .

[49]  G Vriend,et al.  Parameter relation rows: a query system for protein structure function relationships. , 1990, Protein engineering.

[50]  G. Dreyfuss,et al.  Heterogeneous nuclear ribonucleoprotein particles and the pathway of mRNA formation. , 1988, Trends in biochemical sciences.

[51]  H. Busch,et al.  Isolation and characterization of uridylic acid-rich 7 S ribonucleic acid of rat liver nuclei. , 1968, The Journal of biological chemistry.

[52]  C. Eyers Universal sample preparation method for proteome analysis , 2009 .

[53]  P. Güntert Automated NMR structure calculation with CYANA. , 2004, Methods in molecular biology.

[54]  W. Braun,et al.  Automatic assignment of NOESY cross peaks and determination of the protein structure of a new world scorpion neurotoxin using NOAH/DIAMOD. , 2001, Journal of magnetic resonance.