The overarching goal of the proposed research is to elucidate the mechanisms by which synonymous mutations affect the abundance and turnover of synthesized proteins in cytoplasm with ensuing effect on fitness. We determined that synonymous substitutions in the folA gene encoding the essential E. coli enzyme Dihydrofolate Reductase (DHFR) have broad effects: synonymous substitutions of rare codons to frequent ones at the 5' end of the nucleotide sequence cause significant drop of the amount of mRNA produced while the ones near the 3'- terminus result in depletion of soluble, active DHFR protein. We will broadly investigate the relationship between DHFR folding thermodynamics and kinetics and its post-translation abundance in cytoplasm for a broad coverage of sequence space including both missense and synonymous mutations. We will focus on the role that protein quality control (specific proteases and chaperones) play in amplifying or mitigating fitness effects of synonymous mutations and determine the evolutionary paths by which E. coli recovers the fitness losses incurred by specific synonymous mutations. Lessons from the DHFR study will be used as guidance for a broader exploration on the level of complete genomes of several organisms from E. coli to human with the aim to link conservation of specific synonymous codons to the position-specific aspects of protein folding pathways. To this end we will apply our recent algorithm for structure- based predictions of protein folding pathways to predict location of rare conserved codons based on only the three-dimensional structure of the protein. Altogether these studies will provide deep mechanistic insights into the origin of fitness effects of synonymous substitutions and their evolutionary consequences. It will help to discern the forces of evolutionary selection from sequence analysis data. Further, it will enable to identify the causal relationship between mutations and disease phenotype ? an unmet medical need in the era of data driven approaches to development of new therapeutics.
The aim of this research is to elucidate the mechanistic underpinnings of fitness effects of synonymous substitutions. It will enhance our ability to discern the relationships between genetic mutations and disease and develop treatments of disease phenotypes caused by broad classes of mutations.
| Bhattacharyya, Sanchari; Jacobs, William M; Adkar, Bharat V et al. (2018) Accessibility of the Shine-Dalgarno Sequence Dictates N-Terminal Codon Bias in E. coli. Mol Cell 70:894-905.e5 |
| Jacobs, William M; Shakhnovich, Eugene I (2017) Evidence of evolutionary selection for cotranslational folding. Proc Natl Acad Sci U S A 114:11434-11439 |
