Functional analysis of the AUG initiator codon context reveals novel conserved sequences that disfavor mRNA translation in eukaryotes

Author:

Hernández Greco1ORCID,García Alejandra1,Weingarten-Gabbay Shira234,Mishra Rishi Kumar5,Hussain Tanweer5ORCID,Amiri Mehdi6,Moreno-Hagelsieb Gabriel7,Montiel-Dávalos Angélica1,Lasko Paul8,Sonenberg Nahum6

Affiliation:

1. mRNA and Cancer Laboratory, Unit of Biomedical Research on Cancer, National Institute of Cancer (INCan) , Mexico City 14080 , Mexico

2. Broad Institute of MIT and Harvard , Cambridge , MA , USA

3. Department of Organismic and Evolutionary Biology, Harvard University , Cambridge , MA , USA

4. Laboratory of Virology and Infectious Disease, The Rockefeller University , New York , NY , USA

5. Department of Developmental Biology and Genetics, Indian Institute of Science , Bengaluru-560012, India

6. Department of Biochemistry and Goodman Cancer Institute. McGill University., Montreal , QC H3A 1A3 , Canada

7. Department of Biology, Wilfrid Laurier University. 75 University Ave. W, Waterloo , ON N2L 3C5 , Canada

8. Department of Biology, McGill University. Montreal , QC H3G 0B1 , Canada

Abstract

Abstract mRNA translation is a fundamental process for life. Selection of the translation initiation site (TIS) is crucial, as it establishes the correct open reading frame for mRNA decoding. Studies in vertebrate mRNAs discovered that a purine at −3 and a G at +4 (where A of the AUG initiator codon is numbered + 1), promote TIS recognition. However, the TIS context in other eukaryotes has been poorly experimentally analyzed. We analyzed in vitro the influence of the −3, −2, −1 and + 4 positions of the TIS context in rabbit, Drosophila, wheat, and yeast. We observed that −3A conferred the best translational efficiency across these species. However, we found variability at the + 4 position for optimal translation. In addition, the Kozak motif that was defined from mammalian cells was only weakly predictive for wheat and essentially non-predictive for yeast. We discovered eight conserved sequences that significantly disfavored translation. Due to the big differences in translational efficiency observed among weak TIS context sequences, we define a novel category that we termed ‘barren AUG context sequences (BACS)’, which represent sequences disfavoring translation. Analysis of mRNA-ribosomal complexes structures provided insights into the function of BACS. The gene ontology of the BACS-containing mRNAs is presented.

Funder

National Council of Science and Technology, Mexico

National Institute of Cancer

Universidad Nacional Autónoma de México

NSERC

DBT-Welcome Trust India Alliance

Publisher

Oxford University Press (OUP)

Subject

Genetics

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