scholarly journals Covalent catalysis in nucleotidyl transfer. A KTDG motif essential for enzyme-GMP complex formation by mRNA capping enzyme is conserved at the active sites of RNA and DNA ligases.

1993 ◽  
Vol 268 (10) ◽  
pp. 7256-7260 ◽  
Author(s):  
P. Cong ◽  
S. Shuman
Keyword(s):  
Complex Formation ◽  
Active Sites ◽  
Dna Ligases ◽  
Mrna Capping ◽  
Capping Enzyme ◽  
Covalent Catalysis ◽  
Rna And Dna

scholarly journals Mutational analysis of mRNA capping enzyme identifies amino acids involved in GTP binding, enzyme-guanylate formation, and GMP transfer to RNA.

1995 ◽  
Vol 15 (11) ◽  
pp. 6222-6231 ◽  
Author(s):  
P Cong ◽  
S Shuman
Keyword(s):  
Vaccinia Virus ◽  
Active Sites ◽  
Mutational Analysis ◽  
Structural Basis ◽  
Sequence Element ◽  
Termination Factor ◽  
Mrna Capping ◽  
Capping Enzyme ◽  
Rna Capping ◽  
Capping Enzymes

Vaccinia virus mRNA capping enzyme is a multifunctional protein with RNA triphosphatase, RNA guanylyltransferase, RNA (guanine-7) methyltransferase, and transcription termination factor activities. The protein is a heterodimer of 95- and 33-kDa subunits encoded by the vaccinia virus D1 and D12 genes, respectively. The capping reaction entails transfer of GMP from GTP to the 5'-diphosphate end of mRNA via a covalent enzyme-(lysyl-GMP) intermediate. The active site is situated at Lys-260 of the D1 subunit within a sequence element, KxDG (motif I), that is conserved in the capping enzymes from yeasts and other DNA viruses and at the active sites of covalent adenylylation of RNA and DNA ligases. Four additional sequence motifs (II to V) are conserved in the same order and with similar spacing among the capping enzymes and several ATP-dependent ligases. The relevance of these common sequence elements to the RNA capping reaction was addressed by mutational analysis of the vaccinia virus D1 protein. Nine alanine substitution mutations were targeted to motifs II to V. Histidine-tagged versions of the mutated D1 polypeptide were coexpressed in bacteria with the D12 subunit, and the His-tagged heterodimers were purified by Ni affinity and phosphocellulose chromatography steps. Whereas each of the mutated enzymes retained triphosphatase, methyltransferase, and termination factor activities, six of nine mutant enzymes were defective in some aspect of transguanylylation. Individual mutations in motifs III, IV, and V had distinctive effects on the affinity of enzyme for GTP, the rate of covalent catalysis (EpG formation), or the transfer of GMP from enzyme to RNA. These results are concordant with mutational studies of yeast RNA capping enzyme and suggest a conserved structural basis for covalent nucleotidyl transfer.

scholarly journals Interaction of bacteriophage T4 RNA and DNA ligases in joining of duplex DNA at base-paired ends.

1977 ◽  
Vol 252 (11) ◽  
pp. 3987-3994 ◽  
Author(s):  
A Sugino ◽  
H M Goodman ◽  
H L Heyneker ◽  
J Shine ◽  
H W Boyer ◽  
...  
Keyword(s):  
Bacteriophage T4 ◽  
Duplex Dna ◽  
Dna Ligases ◽  
Rna And Dna

scholarly journals Divergent Subunit Interactions among Fungal mRNA 5′-Capping Machineries

2002 ◽  
Vol 1 (3) ◽  
pp. 448-457 ◽  
Author(s):  
Toshimitsu Takagi ◽  
Eun-Jung Cho ◽  
Rozmin T. K. Janoo ◽  
Vladimir Polodny ◽  
Yasutaka Takase ◽  
...  
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Candida Albicans ◽  
Rna Polymerase Ii ◽  
Subunit Interactions ◽  
Pol Ii ◽  
Mrna Capping ◽  
Capping Enzyme ◽  
Enzyme Subunits ◽  
Carboxyl Terminal

ABSTRACT The Saccharomyces cerevisiae mRNA capping enzyme consists of two subunits: an RNA 5′-triphosphatase (RTPase) and GTP::mRNA guanylyltransferase (GTase). The GTase subunit (Ceg1) binds to the phosphorylated carboxyl-terminal domain of the largest subunit (CTD-P) of RNA polymerase II (pol II), coupling capping with transcription. Ceg1 bound to the CTD-P is inactive unless allosterically activated by interaction with the RTPase subunit (Cet1). For purposes of comparison, we characterize here the related GTases and RTPases from the yeasts Schizosaccharomyces pombe and Candida albicans. Surprisingly, the S. pombe capping enzyme subunits do not interact with each other. Both can independently interact with CTD-P of pol II, and the GTase is not repressed by CTD-P binding. The S. pombe RTPase gene (pct1 +) is essential for viability. Pct1 can replace the S. cerevisiae RTPase when GTase activity is supplied by the S. pombe or mouse enzymes but not by the S. cerevisiae GTase. The C. albicans capping enzyme subunits do interact with each other. However, this interaction is not essential in vivo. Our results reveal an unexpected diversity among the fungal capping machineries.

scholarly journals Thermodynamics of ligand binding by the yeast mRNA-capping enzyme reveals different modes of binding

2004 ◽  
Vol 384 (2) ◽  
pp. 411-420 ◽  
Author(s):  
Isabelle BOUGIE ◽  
Amélie PARENT ◽  
Martin BISAILLON
Keyword(s):  
Ligand Binding ◽  
Entropy Change ◽  
Enthalpy Change ◽  
Mrna Capping ◽  
Capping Enzyme ◽  
Eukaryotic Mrnas ◽  
Entropic Effect ◽  
A Minor ◽  
Rna Capping ◽  
Capping Enzymes

RNA-capping enzymes are involved in the synthesis of the cap structure found at the 5′-end of eukaryotic mRNAs. The present study reports a detailed study on the thermodynamic parameters involved in the interaction of an RNA-capping enzyme with its ligands. Analysis of the interaction of the Saccharomyces cerevisiae RNA-capping enzyme (Ceg1) with GTP, RNA and manganese ions revealed significant differences between the binding forces that drive the interaction of the enzyme with its RNA and GTP substrates. Our thermodynamic analyses indicate that the initial association of GTP with the Ceg1 protein is driven by a favourable enthalpy change (ΔH=−80.9 kJ/mol), but is also clearly associated with an unfavourable entropy change (TΔS=−62.9 kJ/mol). However, the interaction between Ceg1 and RNA revealed a completely different mode of binding, where binding to RNA is clearly dominated by a favourable entropic effect (TΔS=20.5 kJ/mol), with a minor contribution from a favourable enthalpy change (ΔH=−5.3 kJ/mol). Fluorescence spectroscopy also allowed us to evaluate the initial binding of GTP to such an enzyme, thereby separating the GTP binding step from the concomitant metal-dependent hydrolysis of GTP that results in the formation of a covalent GMP–protein intermediate. In addition to the determination of the energetics of ligand binding, our study leads to a better understanding of the molecular basis of substrate recognition by RNA-capping enzymes.

scholarly journals Magnesium-Induced Nucleophile Activation in the Guanylyltransferase mRNA Capping Enzyme

Biochemistry ◽  
2012 ◽  
Vol 51 (51) ◽  
pp. 10236-10243 ◽  
Author(s):  
Robert V. Swift ◽  
Chau D. Ong ◽  
Rommie E. Amaro
Keyword(s):  
Mrna Capping ◽  
Capping Enzyme ◽  
Nucleophile Activation

scholarly journals Isolation of the mRNA-capping enzyme and ferric-reductase-related genes from Candida albicans

Microbiology ◽  
1996 ◽  
Vol 142 (9) ◽  
pp. 2515-2523 ◽  
Author(s):  
T. Yamada-Okabe ◽  
O. Shimmi ◽  
R. Doi ◽  
K. Mizumoto ◽  
M. Arisawa ◽  
...  
Keyword(s):  
Candida Albicans ◽  
Ferric Reductase ◽  
Mrna Capping ◽  
Capping Enzyme

scholarly journals A55 Molecular systematics of sturgeon nucleocytoplasmic large DNA viruses

2019 ◽  
Vol 5 (Supplement_1) ◽  
Author(s):  
S Clouthier ◽  
E Anderson ◽  
G Kurath ◽  
R Breyta
Keyword(s):  
Rna Polymerase ◽  
Rna Polymerase Ii ◽  
Dna Sequences ◽  
Small Subunit ◽  
Sequence Length ◽  
Dna Viruses ◽  
Mrna Capping ◽  
Capping Enzyme ◽  
Nucleocytoplasmic Large Dna Virus ◽  
Nucleocytoplasmic Large Dna Viruses

Abstract Namao virus (NV) is a sturgeon nucleocytoplasmic large DNA virus (sNCLDV) that can cause a lethal disease of the integumentary system in lake sturgeon Acipenser fulvescens. As a group, the sNCLDV have not been assigned to any currently recognized taxonomic family of viruses. In this study, a dataset of NV DNA sequences was generated and assembled as two non-overlapping contigs of 306 and 448 base pairs (bp) and then used to conduct a comprehensive systematics analysis using Bayesian phylogenetic inference for NV, other sNCLDV, and representative members of six families of the NCLDV superfamily. The phylogeny of NV was reconstructed using protein homologues encoded by nine nucleocytoplasmic virus orthologous genes (NCVOGs): NCVOG0022—mcp, NCVOG0038—DNA polymerase B elongation subunit, NCVOG0076—VV A18-type helicase, NCVOG0249—VV A32-type ATPase, NCVOG0262—AL2 VLTF3-like transcription factor, NCVOG0271—RNA polymerase II subunit II, NCVOG0274—RNA polymerase II subunit I, NCVOG0276—ribonucleotide reductase small subunit, and NCVOG1117—mRNA capping enzyme. The accuracy of our phylogenetic method was evaluated using a combination of Bayesian statistical analysis and congruence analysis. Stable tree topologies were obtained with datasets differing in target molecule(s), sequence length, and taxa. Congruent topologies were obtained in phylogenies constructed using individual protein datasets and when four proteins were used in a concatenated approach. The major capsid protein phylogeny indicated that ten representative sNCLDV form a monophyletic group comprised of four lineages within a polyphyletic Mimi-Phycodnaviridae group of taxa. Overall, the analyses revealed that Namao virus is a member of the Mimiviridae family with strong and consistent support for a clade containing NV and CroV as sister taxa.

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