A network of hydrophobic residues impeding helix alphaC rotation maintains latency of kinase Gcn2, which phosphorylates the alpha subunit of translation initiation factor 2.

Abstract

Kinase Gcn2 is activated by amino acid starvation and downregulates translation initiation by phosphorylating the alpha subunit of translation initiation factor 2 (eIF2alpha). The Gcn2 kinase domain (KD) is inert and must be activated by tRNA binding to the adjacent regulatory domain. Previous work indicated that Saccharomyces cerevisiae Gcn2 latency results from inflexibility of the hinge connecting the N and C lobes and a partially obstructed ATP-binding site in the KD. Here, we provide strong evidence that a network of hydrophobic interactions centered on Leu-856 also promotes latency by constraining helix alphaC rotation in the KD in a manner relieved during amino acid starvation by tRNA binding and autophosphorylation of Thr-882 in the activation loop. Thus, we show that mutationally disrupting the hydrophobic network in various ways constitutively activates eIF2alpha phosphorylation in vivo and bypasses the requirement for a key tRNA binding motif (m2) and Thr-882 in Gcn2. In particular, replacing Leu-856 with any nonhydrophobic residue activates Gcn2, while substitutions with various hydrophobic residues maintain kinase latency. We further provide strong evidence that parallel, back-to-back dimerization of the KD is a step on the Gcn2 activation pathway promoted by tRNA binding and autophosphorylation. Remarkably, mutations that disrupt the L856 hydrophobic network or enhance hinge flexibility eliminate the need for the conserved salt bridge at the parallel dimer interface, implying that KD dimerization facilitates the reorientation of alphaC and remodeling of the active site for enhanced ATP binding and catalysis. We propose that hinge remodeling, parallel dimerization, and reorientation of alphaC are mutually reinforcing conformational transitions stimulated by tRNA binding and secured by the ensuing autophosphorylation of T882 for stable kinase activation.

• Authors: Andrés Gárriz, Hongfang Qiu, Madhusudan Dey, Eun-Joo Seo, Thomas E Dever, Alan G Hinnebusch
• Journal: Molecular and cellular biology (Mol Cell Biol) Vol. 29 Issue 6 Pg. 1592-607 (Mar 2009) ISSN: 1098-5549 [Electronic] United States
• PMID: 19114556 (Publication Type: Journal Article, Research Support, N.I.H., Intramural)

Chemical References

• Eukaryotic Initiation Factor-2
• Protein Subunits
• Saccharomyces cerevisiae Proteins
• RNA, Transfer
• GCN2 protein, S cerevisiae
• Protein Serine-Threonine Kinases

Topics

• Amino Acid Substitution
• Enzyme Activation
• Eukaryotic Initiation Factor-2 (chemistry, genetics, metabolism)
• Hydrophobic and Hydrophilic Interactions
• Models, Molecular
• Mutation
• Phosphorylation
• Protein Multimerization
• Protein Serine-Threonine Kinases (chemistry, genetics, metabolism)
• Protein Structure, Secondary
• Protein Subunits (chemistry, genetics, metabolism)
• RNA, Transfer (metabolism)
• Saccharomyces cerevisiae (metabolism)
• Saccharomyces cerevisiae Proteins (chemistry, genetics, metabolism)