Insertions and deletions in the RNA sequence-structure map

• Published in: Journal of the Royal Society interface 2021-10, Vol.18 (183), p.20210380
• Main Authors: Martin, Nora S, Ahnert, Sebastian E
• Format: Article
• Language: English
• Subjects: Base Sequence; Evolution, Molecular; Genotype; INDEL Mutation; Life Sciences–Physics interface; Models, Genetic; Mutation; RNA - genetics
• ISSN: 1742-5662; 1742-5689; 1742-5662
• DOI: 10.1098/rsif.2021.0380

Genotype-phenotype maps link genetic changes to their fitness effect and are thus an essential component of evolutionary models. The map between RNA sequences and their secondary structures is a key example and has applications in functional RNA evolution. For this map, the structural effect of substitutions is well understood, but models usually assume a constant sequence length and do not consider insertions or deletions. Here, we expand the sequence-structure map to include single nucleotide insertions and deletions by using the RNAshapes concept. To quantify the structural effect of insertions and deletions, we generalize existing definitions for robustness and non-neutral mutation probabilities. We find striking similarities between substitutions, deletions and insertions: robustness to substitutions is correlated with robustness to insertions and, for most structures, to deletions. In addition, frequent structural changes after substitutions also tend to be common for insertions and deletions. This is consistent with the connection between energetically suboptimal folds and possible structural transitions. The similarities observed hold both for genotypic and phenotypic robustness and mutation probabilities, i.e. for individual sequences and for averages over sequences with the same structure. Our results could have implications for the rate of neutral and non-neutral evolution.