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Modeling the Effect of RRNA-mRNA Interactions and MRNA Folding on MRNA Translation in Chloroplasts

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Specialty Biotechnology
Date 2022 Jun 10
PMID 35685358
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Abstract

The process of translation initiation in prokaryotes is mediated by the hybridization of the 16S rRNA of the small ribosomal subunit with the mRNA in a short region called the ribosomal binding site. However, translation initiation in chloroplasts, which have evolved from an ancestral bacterium, is not well understood. Some studies suggest that in many cases it differs from translation initiation in bacteria and involves various novel interactions of the mRNA structures with intracellular factors; however currently, there is no generic quantitative model related to these aspects in chloroplasts. We developed a novel computational pipeline and models that can be used for understanding and modeling translation regulation in chloroplasts. We demonstrate that local folding and co-folding energy of the rRNA and the mRNA correlates with codon usage estimators of expression levels (r = -0.63) and infer predictive models that connect these energies and codon usage to protein levels (with correlation up to 0.71). In addition, we demonstrate that the ends of the transcripts in chloroplasts are populated with various structural elements that may be functional. Furthermore, we report a database of 166 novel structures in the chloroplast transcripts that are predicted to be functional. We believe that the models reported here improve existing understandings of genomic evolution and the biophysics of translation in chloroplasts; as such, they can aid gene expression engineering in chloroplasts for various biotechnological objectives.

Citing Articles

Tandem repeats ubiquitously flank and contribute to translation initiation sites.

Maddi A, Kavousi K, Arabfard M, Ohadi H, Ohadi M BMC Genom Data. 2022; 23(1):59.

PMID: 35896982 PMC: 9331589. DOI: 10.1186/s12863-022-01075-5.

References
1.
Strenkert D, Schmollinger S, Gallaher S, Salome P, Purvine S, Nicora C . Multiomics resolution of molecular events during a day in the life of Chlamydomonas. Proc Natl Acad Sci U S A. 2019; 116(6):2374-2383. PMC: 6369806. DOI: 10.1073/pnas.1815238116. View

2.
Lorenz R, Bernhart S, Honer Zu Siederdissen C, Tafer H, Flamm C, Stadler P . ViennaRNA Package 2.0. Algorithms Mol Biol. 2011; 6:26. PMC: 3319429. DOI: 10.1186/1748-7188-6-26. View

3.
Ben-Yehezkel T, Atar S, Zur H, Diament A, Goz E, Marx T . Rationally designed, heterologous S. cerevisiae transcripts expose novel expression determinants. RNA Biol. 2015; 12(9):972-84. PMC: 4615757. DOI: 10.1080/15476286.2015.1071762. View

4.
Hirose T, Kusumegi T, Sugiura M . Translation of tobacco chloroplast rps14 mRNA depends on a Shine-Dalgarno-like sequence in the 5'-untranslated region but not on internal RNA editing in the coding region. FEBS Lett. 1998; 430(3):257-60. DOI: 10.1016/s0014-5793(98)00673-5. View

5.
Shine J, Dalgarno L . The 3'-terminal sequence of Escherichia coli 16S ribosomal RNA: complementarity to nonsense triplets and ribosome binding sites. Proc Natl Acad Sci U S A. 1974; 71(4):1342-6. PMC: 388224. DOI: 10.1073/pnas.71.4.1342. View