Human TRMT112-Methyltransferase Network Consists of Seven Partners Interacting with a Common Co-Factor

被引:16
作者
Brumele, Baiba [1 ]
Mutso, Margit [1 ]
Telanne, Lilian [1 ]
ounap, Kadri [1 ]
Spunde, Karina [1 ]
Abroi, Aare [1 ]
Kurg, Reet [1 ]
机构
[1] Univ Tartu, Inst Technol, EE-50411 Tartu, Estonia
关键词
methyltransferase; TRMT112; RNA methylation; ribosome biogenesis; protein stabilisation; 18S RIBOSOMAL-RNA; GENE ONTOLOGY; METHYLTRANSFERASE; TRM112; TRANSLATION; METHYLATION; HOMOLOG; PROTEIN;
D O I
10.3390/ijms222413593
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Methylation is an essential epigenetic modification mainly catalysed by S-Adenosyl methionine-dependent methyltransferases (MTases). Several MTases require a cofactor for their metabolic stability and enzymatic activity. TRMT112 is a small evolutionary conserved protein that acts as a co-factor and activator for different MTases involved in rRNA, tRNA and protein methylation. Using a SILAC screen, we pulled down seven methyltransferases-N6AMT1, WBSCR22, METTL5, ALKBH8, THUMPD2, THUMPD3 and TRMT11-as interaction partners of TRMT112. We showed that TRMT112 stabilises all seven MTases in cells. TRMT112 and MTases exhibit a strong mutual feedback loop when expressed together in cells. TRMT112 interacts with its partners in a similar way; however, single amino acid mutations on the surface of TRMT112 reveal several differences as well. In summary, mammalian TRMT112 can be considered as a central "hub" protein that regulates the activity of at least seven methyltransferases.
引用
收藏
页数:17
相关论文
共 41 条
  • [1] Gene Ontology: tool for the unification of biology
    Ashburner, M
    Ball, CA
    Blake, JA
    Botstein, D
    Butler, H
    Cherry, JM
    Davis, AP
    Dolinski, K
    Dwight, SS
    Eppig, JT
    Harris, MA
    Hill, DP
    Issel-Tarver, L
    Kasarskis, A
    Lewis, S
    Matese, JC
    Richardson, JE
    Ringwald, M
    Rubin, GM
    Sherlock, G
    [J]. NATURE GENETICS, 2000, 25 (01) : 25 - 29
  • [2] Cardiac mitochondrial function depends on BUD23 mediated ribosome programming
    Baxter, Matthew
    Voronkov, Maria
    Poolman, Toryn
    Galli, Gina
    Pinali, Christian
    Goosey, Laurence
    Knight, Abigail
    Krakowiak, Karolina
    Maidstone, Robert
    Iqbal, Mudassar
    Zi, Min
    Prehar, Sukhpal
    Cartwright, Elizabeth J.
    Gibbs, Julie
    Matthews, Laura C.
    Adamson, Antony D.
    Humphreys, Neil E.
    Rebelo-Guiomar, Pedro
    Minczuk, Michal
    Bechtold, David A.
    Loudon, Andrew
    Ray, David
    [J]. ELIFE, 2020, 9
  • [3] Trm112, a Protein Activator of Methyltransferases Modifying Actors of the Eukaryotic Translational Apparatus
    Bourgeois, Gabrielle
    Letoquart, Juliette
    Nhan van Tran
    Graille, Marc
    [J]. BIOMOLECULES, 2017, 7 (01):
  • [4] Activation mode of the eukaryotic m2G10 tRNA methyltransferase Trm11 by its partner protein Trm112
    Bourgeois, Gabrielle
    Marcoux, Julien
    Saliou, Jean-Michel
    Cianferani, Sarah
    Graille, Marc
    [J]. NUCLEIC ACIDS RESEARCH, 2017, 45 (04) : 1971 - 1982
  • [5] The Gene Ontology resource: enriching a GOld mine
    Carbon, Seth
    Douglass, Eric
    Good, Benjamin M.
    Unni, Deepak R.
    Harris, Nomi L.
    Mungall, Christopher J.
    Basu, Siddartha
    Chisholm, Rex L.
    Dodson, Robert J.
    Hartline, Eric
    Fey, Petra
    Thomas, Paul D.
    Albou, Laurent-Philippe
    Ebert, Dustin
    Kesling, Michael J.
    Mi, Huaiyu
    Muruganujan, Anushya
    Huang, Xiaosong
    Mushayahama, Tremayne
    LaBonte, Sandra A.
    Siegele, Deborah A.
    Antonazzo, Giulia
    Attrill, Helen
    Brown, Nick H.
    Garapati, Phani
    Marygold, Steven J.
    Trovisco, Vitor
    Dos Santos, Gil
    Falls, Kathleen
    Tabone, Christopher
    Zhou, Pinglei
    Goodman, Joshua L.
    Strelets, Victor B.
    Thurmond, Jim
    Garmiri, Penelope
    Ishtiaq, Rizwan
    Rodriguez-Lopez, Milagros
    Acencio, Marcio L.
    Kuiper, Martin
    Laegreid, Astrid
    Logie, Colin
    Lovering, Ruth C.
    Kramarz, Barbara
    Saverimuttu, Shirin C. C.
    Pinheiro, Sandra M.
    Gunn, Heather
    Su, Renzhi
    Thurlow, Katherine E.
    Chibucos, Marcus
    Giglio, Michelle
    [J]. NUCLEIC ACIDS RESEARCH, 2021, 49 (D1) : D325 - D334
  • [6] The ribosome: A hot spot for the identification of new types of protein methyltransferases
    Clarke, Steven G.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2018, 293 (27) : 10438 - 10446
  • [7] rRNA modifications and ribosome function
    Decatur, WA
    Fournier, MJ
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2002, 27 (07) : 344 - 351
  • [8] HemK2 protein, encoded on human chromosome 21, methylates translation termination factor eRF1
    Figaro, Sabine
    Scrima, Nathalie
    Buckingham, Richard H.
    Heurgue-Hamard, Valerie
    [J]. FEBS LETTERS, 2008, 582 (16): : 2352 - 2356
  • [9] Trm112 Is Required for Bud23-Mediated Methylation of the 18S rRNA at Position G1575
    Figaro, Sabine
    Wacheul, Ludivine
    Schillewaert, Stephanie
    Graille, Marc
    Huvelle, Emmeline
    Mongeard, Remi
    Zorbas, Christiane
    Lafontaine, Denis L. J.
    Heurgue-Hamard, Valerie
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2012, 32 (12) : 2254 - 2267
  • [10] Human AlkB Homolog ABH8 Is a tRNA Methyltransferase Required for Wobble Uridine Modification and DNA Damage Survival
    Fu, Dragony
    Brophy, Jennifer A. N.
    Chan, Clement T. Y.
    Atmore, Kyle A.
    Begley, Ulrike
    Paules, Richard S.
    Dedon, Peter C.
    Begley, Thomas J.
    Samson, Leona D.
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2010, 30 (10) : 2449 - 2459