High resolution cryoEM of mammalian mitoribosomes revealed the unexpected presence of mitochondrially encoded tRNA as a structural component of mitochondrial large ribosomal subunit (mt-LSU). Our previously published data identified that only mitochondrial (mt-) tRNA and mt-tRNA can be incorporated into mammalian mt-LSU and within an organism there is no evidence of tissue specific variation. When mt-tRNA is limiting, human mitoribosomes can integrate mt-tRNA instead to generate a translationally competent monosome. Here we discuss the possible reasons for and consequences of the observed plasticity of the structural mt-tRNA integration. We also indicate potential direction for further research that could help our understanding of the mechanistic and evolutionary aspects of this unprecedented system.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731804 | PMC |
http://dx.doi.org/10.1080/15476286.2017.1356551 | DOI Listing |
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