133 research outputs found
The yeast ribosome synthesis factor Emg1 is a novel member of the superfamily of alpha/beta knot fold methyltransferases
Emg1 was previously shown to be required for maturation of the 18S rRNA and biogenesis of the 40S ribosomal subunit. Here we report the determination of the crystal structure of Emg1 at 2 Å resolution in complex with the methyl donor, S-adenosyl-methionine (SAM). This structure identifies Emg1 as a novel member of the alpha/beta knot fold methyltransferase (SPOUT) superfamily. In addition to the conserved SPOUT core, Emg1 has two unique domains that form an extended surface, which we predict to be involved in binding of RNA substrates. A point mutation within a basic patch on this surface almost completely abolished RNA binding in vitro. Three point mutations designed to disrupt the interaction of Emg1 with SAM each caused>100-fold reduction in SAM binding in vitro. Expression of only Emg1 with these mutations could support growth and apparently normal ribosome biogenesis in strains genetically depleted of Emg1. We conclude that the catalytic activity of Emg1 is not essential and that the presence of the protein is both necessary and sufficient for ribosome biogenesis
Crystal structures of the Gon7/Pcc1 and Bud32/Cgi121 complexes provide a model for the complete yeast KEOPS complex.
International audienceThe yeast KEOPS protein complex comprising Kae1, Bud32, Cgi121, Pcc1 and Gon7 is responsible for the essential tRNA threonylcarbamoyladenosine (t(6)A) modification. Deletion of genes coding for the KEOPS subunits also affects telomere elongation and transcriptional regulation. In the present work, the crystal structure of Bud32/Cgi121 in complex with ADP revealed that ADP is bound in the catalytic site of Bud32 in a canonical manner characteristic of Protein Kinase A (PKA) family proteins. We found that Gon7 forms a stable heterodimer with Pcc1 and report the crystal structure of the Pcc1-Gon7 heterodimer. Gon7 interacts with the same Pcc1 region engaged in the archaeal Pcc1 homodimer. We further show that yeast KEOPS, unlike its archaeal counterpart, exists as a heteropentamer in which Gon7, Pcc1, Kae1, Bud32 and Cgi121 also adopt a linear arrangement. We constructed a model of yeast KEOPS that provides structural insight into the role of Gon7. The model also revealed the presence of a highly positively charged crater surrounding the entrance of Kae1 that likely binds tRNA
Mechanism of activation of methyltransferases involved in translation by the Trm112 ‘hub’ protein
Methylation is a common modification encountered in DNA, RNA and proteins. It plays a central role in gene expression, protein function and mRNA translation. Prokaryotic and eukaryotic class I translation termination factors are methylated on the glutamine of the essential and universally conserved GGQ motif, in line with an important cellular role. In eukaryotes, this modification is performed by the Mtq2-Trm112 holoenzyme. Trm112 activates not only the Mtq2 catalytic subunit but also two other tRNA methyltransferases (Trm9 and Trm11). To understand the molecular mechanisms underlying methyltransferase activation by Trm112, we have determined the 3D structure of the Mtq2-Trm112 complex and mapped its active site. Using site-directed mutagenesis and in vivo functional experiments, we show that this structure can also serve as a model for the Trm9-Trm112 complex, supporting our hypothesis that Trm112 uses a common strategy to activate these three methyltransferases
Kinetic Theory of Plasmas: Translational Energy
In the present contribution, we derive from kinetic theory a unified fluid
model for multicomponent plasmas by accounting for the electromagnetic field
influence. We deal with a possible thermal nonequilibrium of the translational
energy of the particles, neglecting their internal energy and the reactive
collisions. Given the strong disparity of mass between the electrons and heavy
particles, such as molecules, atoms, and ions, we conduct a dimensional
analysis of the Boltzmann equation. We then generalize the Chapman-Enskog
method, emphasizing the role of a multiscale perturbation parameter on the
collisional operator, the streaming operator, and the collisional invariants of
the Boltzmann equation. The system is examined at successive orders of
approximation, each of which corresponding to a physical time scale. The
multicomponent Navier-Stokes regime is reached for the heavy particles, which
follow a hyperbolic scaling, and is coupled to first order drift-diffusion
equations for the electrons, which follow a parabolic scaling. The transport
coefficients exhibit an anisotropic behavior when the magnetic field is strong
enough. We also give a complete description of the Kolesnikov effect, i.e., the
crossed contributions to the mass and energy transport fluxes coupling the
electrons and heavy particles. Finally, the first and second principles of
thermodynamics are proved to be satisfied by deriving a total energy equation
and an entropy equation. Moreover, the system of equations is shown to be
conservative and the purely convective system hyperbolic, thus leading to a
well-defined structure
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