The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Interaction Profiling Identifies the Human Nuclear Exosome Targeting Complex
Abstract
The RNA exosome is a conserved degradation machinery, which obtains full activity only when associated with cofactors. The most prominent activator of the yeast nuclear exosome is the RNA helicase Mtr4p, acting in the context of the Trf4p/Air2p/Mtr4p polyadenylation (TRAMP) complex. The existence of a similar activator(s) in humans remains elusive. By establishing an interaction network of the human nuclear exosome, we identify the trimeric Nuclear Exosome Targeting (NEXT) complex, containing hMTR4, the Zn-knuckle protein ZCCHC8, and the putative RNA binding protein RBM7. ZCCHC8 and RBM7 are excluded from nucleoli, and consistently NEXT is specifically required for the exosomal degradation of promoter upstream transcripts (PROMPTs). We also detect putative homolog TRAMP subunits hTRF4-2 (Trf4p) and ZCCHC7 (Air2p) in hRRP6 and hMTR4 precipitates. However, at least ZCCHC7 function is restricted to nucleoli. Our results suggest that human nuclear exosome degradation pathways comprise modules of spatially organized cofactors that diverge from the yeast model.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“We found a robust interaction between YTHDC1 and ZCCHC8, but no interaction between YTHDC1 and MTR4 (Figure 2—figure supplement 1B).”
From YTHDC1 mediates nuclear export of N6-methyladenosine methylated mRNAs (2017) · cites this paper as Lubas et al., 2011
Citations
Cites
Cox, J., & Mann, M. (2008) · Nature Biotechnology · doi:10.1038/nbt.1511 · Cited by 14,855
Global analysis of protein expression in yeast
Ghaemmaghami, S., Huh, W.-K., Bower, K., Howson, R. W., Belle, A., Dephoure, N., O'Shea, E. K., & Weissman, J. S. (2003) · Nature · doi:10.1038/nature02046 · Cited by 3,750
Research works printed but not linked: 53
- Allmang, 1999, Functions of the exosome in rRNA, snoRNA and snRNA synthesis, EMBO J., 18, 5399, 10.1093/emboj/18.19.5399 · DOI
- Anderson, 1998, The 3′ to 5′ degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3′ to 5′ exonucleases of the exosome complex, EMBO J., 17, 1497, 10.1093/emboj/17.5.1497 · DOI
- Brown, 2000, The yeast antiviral proteins Ski2p, Ski3p, and Ski8p exist as a complex in vivo, RNA, 6, 449, 10.1017/S1355838200991787 · DOI
- Cristodero, 2007, Trypanosome MTR4 is involved in rRNA processing, Nucleic Acids Res., 35, 7023, 10.1093/nar/gkm736 · DOI
- de la Cruz, 1998, Dob1p (Mtr4p) is a putative ATP-dependent RNA helicase required for the 3′ end formation of 5.8S rRNA in Saccharomyces cerevisiae, EMBO J., 17, 1128, 10.1093/emboj/17.4.1128 · DOI
- Dez, 2007, Roles of the HEAT repeat proteins Utp10 and Utp20 in 40S ribosome maturation, RNA, 13, 1516, 10.1261/rna.609807 · DOI
- Etheridge, 2009, Identification and characterization of nuclear non-canonical poly(A) polymerases from Trypanosoma brucei, Mol. Biochem. Parasitol., 164, 66, 10.1016/j.molbiopara.2008.11.004 · DOI
- Gallenberger, 2010, Lack of WDR36 leads to preimplantation embryonic lethality in mice and delays the formation of small subunit ribosomal RNA in human cells in vitro, Hum. Mol. Genet., 20, 422, 10.1093/hmg/ddq478 · DOI
- Gruber, 2009, Ars2 links the nuclear cap-binding complex to RNA interference and cell proliferation, Cell, 138, 328, 10.1016/j.cell.2009.04.046 · DOI
- Guo, 2003, Spermatogenetic expression of RNA-binding motif protein 7, a protein that interacts with splicing factors, J. Androl., 24, 204, 10.1002/j.1939-4640.2003.tb02664.x · DOI
- Gustafson, 2005, Zcchc8 is a glycogen synthase kinase-3 substrate that interacts with RNA-binding proteins, Biochem. Biophys. Res. Commun., 338, 1359, 10.1016/j.bbrc.2005.10.090 · DOI
- Houseley, 2006, Yeast Trf5p is a nuclear poly(A) polymerase, EMBO Rep., 7, 205, 10.1038/sj.embor.7400612 · DOI
- Houseley, 2008, The nuclear RNA surveillance machinery: the link between ncRNAs and genome structure in budding yeast?, Biochim. Biophys. Acta, 1779, 239, 10.1016/j.bbagrm.2007.12.008 · DOI
- Houseley, 2009, The many pathways of RNA degradation, Cell, 136, 763, 10.1016/j.cell.2009.01.019 · DOI
- Kammler, 2008, The RNA exosome component hRrp6 is a target for 5-fluorouracil in human cells, Mol. Cancer Res., 6, 990, 10.1158/1541-7786.MCR-07-2217 · DOI
- LaCava, 2005, RNA degradation by the exosome is promoted by a nuclear polyadenylation complex, Cell, 121, 713, 10.1016/j.cell.2005.04.029 · DOI
- Lejeune, 2003, Nonsense-mediated mRNA decay in mammalian cells involves decapping, deadenylating, and exonucleolytic activities, Mol. Cell, 12, 675, 10.1016/S1097-2765(03)00349-6 · DOI
- Lykke-Andersen, 2006, CUT it out: silencing of noise in the transcriptome, Nat. Struct. Mol. Biol., 13, 860, 10.1038/nsmb1006-860 · DOI
- Lykke-Andersen, 2009, Origins and activities of the eukaryotic exosome, J. Cell Sci., 122, 1487, 10.1242/jcs.047399 · DOI
- Lykke-Andersen, 2011, The eukaryotic RNA exosome: Same scaffold but variable catalytic subunits, RNA Biol., 8, 61, 10.4161/rna.8.1.14237 · DOI
- McMahon, 2010, Ribosomal 18 S RNA processing by the IGF-I-responsive WDR3 protein is integrated with p53 function in cancer cell proliferation, J. Biol. Chem., 285, 18309, 10.1074/jbc.M110.108555 · DOI
- Milligan, 2005, A nuclear surveillance pathway for mRNAs with defective polyadenylation, Mol. Cell. Biol., 25, 9996, 10.1128/MCB.25.22.9996-10004.2005 · DOI
- Milligan, 2008, A yeast exosome cofactor, Mpp6, functions in RNA surveillance and in the degradation of noncoding RNA transcripts, Mol. Cell. Biol., 28, 5446, 10.1128/MCB.00463-08 · DOI
- Mitchell, 1997, The exosome: a conserved eukaryotic RNA processing complex containing multiple 3′→5′ exoribonucleases, Cell, 91, 457, 10.1016/S0092-8674(00)80432-8 · DOI
- Mitchell, 2003, Rrp47p is an exosome-associated protein required for the 3′ processing of stable RNAs, Mol. Cell. Biol., 23, 6982, 10.1128/MCB.23.19.6982-6992.2003 · DOI
- Mullen, 2008, Degradation of histone mRNA requires oligouridylation followed by decapping and simultaneous degradation of the mRNA both 5′ to 3′ and 3′ to 5′, Genes Dev., 22, 50, 10.1101/gad.1622708 · DOI
- Nakamura, 2008, TRF4 is involved in polyadenylation of snRNAs in Drosophila melanogaster, Mol. Cell. Biol., 28, 6620, 10.1128/MCB.00448-08 · DOI
- Nielsen, 2009, Ars2 and the cap-binding complex team up for silencing, Cell, 138, 224, 10.1016/j.cell.2009.07.009 · DOI
- Ong, 2003, Mass spectrometric-based approaches in quantitative proteomics, Methods, 29, 124, 10.1016/S1046-2023(02)00303-1 · DOI
- Peng, 2003, A panoramic view of yeast noncoding RNA processing, Cell, 113, 919, 10.1016/S0092-8674(03)00466-5 · DOI
- Preker, 2008, RNA exosome depletion reveals transcription upstream of active human promoters, Science, 322, 1851, 10.1126/science.1164096 · DOI
- Preker, 2011, PROMoter uPstream Transcripts share characteristics with mRNAs and are produced upstream of all three major types of mammalian promoters, Nucleic Acids Res., 10.1093/nar/gkr370 · DOI
- Reis, 2007, Contribution of Trf4/5 and the nuclear exosome to genome stability through regulation of histone mRNA levels in Saccharomyces cerevisiae, Genetics, 175, 993, 10.1534/genetics.106.065987 · DOI
- Rougemaille, 2007, Dissecting mechanisms of nuclear mRNA surveillance in THO/sub2 complex mutants, EMBO J., 26, 2317, 10.1038/sj.emboj.7601669 · DOI
- Sabin, 2009, Ars2 regulates both miRNA- and siRNA- dependent silencing and suppresses RNA virus infection in Drosophila, Cell, 138, 340, 10.1016/j.cell.2009.04.045 · DOI
- San Paolo, 2009, Distinct roles of non-canonical poly(A) polymerases in RNA metabolism, PLoS Genet., 5, e1000555, 10.1371/journal.pgen.1000555 · DOI
- Schilders, 2008, Biochemical studies of the mammalian exosome with intact cells, Methods Enzymol., 448, 211, 10.1016/S0076-6879(08)02611-6 · DOI
- Schilders, 2007, C1D and hMtr4p associate with the human exosome subunit PM/Scl-100 and are involved in pre-rRNA processing, Nucleic Acids Res., 35, 2564, 10.1093/nar/gkm082 · DOI · Paper page
- Schmidt, 2010, The human cytoplasmic RNA terminal U-transferase ZCCHC11 targets histone mRNAs for degradation, RNA, 17, 39, 10.1261/rna.2252511 · DOI
- Shcherbik, 2010, Polyadenylation and degradation of incomplete RNA polymerase I transcripts in mammalian cells, EMBO Rep., 11, 106, 10.1038/embor.2009.271 · DOI
- Staals, 2010, Dis3-like 1: a novel exoribonuclease associated with the human exosome, EMBO J., 29, 2358, 10.1038/emboj.2010.122 · DOI
- Stead, 2007, The PMC2NT domain of the catalytic exosome subunit Rrp6p provides the interface for binding with its cofactor Rrp47p, a nucleic acid-binding protein, Nucleic Acids Res., 35, 5556, 10.1093/nar/gkm614 · DOI
- Tomecki, 2010, The human core exosome interacts with differentially localized processive RNases: hDIS3 and hDIS3L, EMBO J., 29, 2342, 10.1038/emboj.2010.121 · DOI
- Torchet, 2002, Processing of 3′-extended read-through transcripts by the exosome can generate functional mRNAs, Mol. Cell, 9, 1285, 10.1016/S1097-2765(02)00544-0 · DOI
- van Dijk, 2007, Human cell growth requires a functional cytoplasmic exosome, which is involved in various mRNA decay pathways, RNA, 13, 1027, 10.1261/rna.575107 · DOI
- van Hoof, 2000, Yeast exosome mutants accumulate 3′-extended polyadenylated forms of U4 small nuclear RNA and small nucleolar RNAs, Mol. Cell. Biol., 20, 441, 10.1128/MCB.20.2.441-452.2000 · DOI
- Vasiljeva, 2006, Nrd1 interacts with the nuclear exosome for 3′ processing of RNA polymerase II transcripts, Mol. Cell, 21, 239, 10.1016/j.molcel.2005.11.028 · DOI
- Weir, 2010, Structural analysis reveals the characteristic features of Mtr4, a DExH helicase involved in nuclear RNA processing and surveillance, Proc. Natl. Acad. Sci. USA, 107, 12139, 10.1073/pnas.1004953107 · DOI
- Wery, 2009, The nuclear poly(A) polymerase and Exosome cofactor Trf5 is recruited cotranscriptionally to nucleolar surveillance, RNA, 15, 406, 10.1261/rna.1402709 · DOI
- Wilson, 2008, ARS2 is a conserved eukaryotic gene essential for early mammalian development, Mol. Cell. Biol., 28, 1503, 10.1128/MCB.01565-07 · DOI
- Win, 2006, Requirement of fission yeast Cid14 in polyadenylation of rRNAs, Mol. Cell. Biol., 26, 1710, 10.1128/MCB.26.5.1710-1721.2006 · DOI
- Wlotzka, 2011, The nuclear RNA polymerase II surveillance system targets polymerase III transcripts, EMBO J., 30, 2982, 10.1038/emboj.2011.209 · DOI
- Wyers, 2005, Cryptic pol II transcripts are degraded by a nuclear quality control pathway involving a new poly(A) polymerase, Cell, 121, 725, 10.1016/j.cell.2005.04.030 · DOI
Cited by
YTHDC1 mediates nuclear export of N6-methyladenosine methylated mRNAs
Roundtree, I. A., Luo, G.-Z., Zhang, Z., Wang, X., Zhou, T., Cui, Y., Sha, J., Huang, X., Guerrero, L., Xie, P., et al. (2017) · eLife · doi:10.7554/elife.31311 · Cited by 1,256
Global, quantitative and dynamic mapping of protein subcellular localization
Itzhak, D. N., Tyanova, S., Cox, J., & Borner, G. H. (2016) · eLife · doi:10.7554/elife.16950 · Cited by 649
Regulation of long non-coding RNAs and genome dynamics by the RNA surveillance machinery
Nair, L., Chung, H., & Basu, U. (2020) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-019-0209-0 · Cited by 203
Weick, E.-M., Puno, M. R., Januszyk, K., Zinder, J. C., DiMattia, M. A., & Lima, C. D. (2018) · Cell · doi:10.1016/j.cell.2018.05.041 · Cited by 153
Cell fitness screens reveal a conflict between LINE-1 retrotransposition and DNA replication
Ardeljan, D., Steranka, J. P., Liu, C., Li, Z., Taylor, M. S., Payer, L. M., Gorbounov, M., Sarnecki, J. S., Deshpande, V., Hruban, R. H., et al. (2020) · Nature Structural & Molecular Biology · doi:10.1038/s41594-020-0372-1 · Cited by 135
Metadata
- Authors
- Lubas, M., Christensen, M. S., Kristiansen, M. S., Domanski, M., Falkenby, L. G., Lykke-Andersen, S., Andersen, J. S., Dziembowski, A., & Jensen, T. H.
- Venue
- Molecular Cell
- Publisher
- Elsevier BV
- Published
- 2011-08
- Volume
- 43
- Issue
- 4
- Pages
- 624-637
- ISSN
- 1097-2765
- Cited by
- 460
- References
- 2
- Language
- en
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 752 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.