6NLQ

Human Mitochondrial Alanyl-tRNA Synthetase C-terminal domain

Summary for 6NLQ

• Entry DOI: 10.2210/pdb6nlq/pdb
• Descriptor: Alanine--tRNA ligase, mitochondrial, CALCIUM ION (3 entities in total)
• Functional Keywords: alanyl-trna synthetase, c-terminal domain, alpha-beta domain, ligase
• Biological source: Homo sapiens (Human)
• Total number of polymer chains: 4
• Total formula weight: 47226.60

Authors

Kuhle, B.,Schimmel, P. (deposition date: 2019-01-08, release date: 2020-01-15, Last modification date: 2023-10-11)

Primary citation

Kuhle, B.,Chihade, J.,Schimmel, P.
Relaxed sequence constraints favor mutational freedom in idiosyncratic metazoan mitochondrial tRNAs.
Nat Commun, 11:969-969, 2020

PubMed Abstract: Metazoan complexity and life-style depend on the bioenergetic potential of mitochondria. However, higher aerobic activity and genetic drift impose strong mutation pressure and risk of irreversible fitness decline in mitochondrial (mt)DNA-encoded genes. Bilaterian mitochondria-encoded tRNA genes, key players in mitochondrial activity, have accumulated mutations at significantly higher rates than their cytoplasmic counterparts, resulting in foreshortened and fragile structures. Here we show that fragility of mt tRNAs coincided with the evolution of bilaterian animals. We demonstrate that bilaterians compensated for this reduced structural complexity in mt tRNAs by sequence-independent induced-fit adaption to the cognate mitochondrial aminoacyl-tRNA synthetase (aaRS). Structural readout by nuclear-encoded aaRS partners relaxed the sequence constraints on mt tRNAs and facilitated accommodation of functionally disruptive mutational insults by cis-acting epistatic compensations. Our results thus suggest that mutational freedom in mt tRNA genes is an adaptation to increased mutation pressure that was associated with the evolution of animal complexity.

PubMed: 32080176
DOI: 10.1038/s41467-020-14725-y

Experimental method

X-RAY DIFFRACTION (1.15 Å)