Rubisco evolution in C? eudicots: an analysis of Amaranthaceae sensu lato.

ABSTRACT:

Background

Rubisco (ribulose-1,5-bisphosphate carboxylase/oxygenase) catalyses the key reaction in the photosynthetic assimilation of CO?. In C? plants CO? is supplied to Rubisco by an auxiliary CO?-concentrating pathway that helps to maximize the carboxylase activity of the enzyme while suppressing its oxygenase activity. As a consequence, C? Rubisco exhibits a higher maximum velocity but lower substrate specificity compared with the C? enzyme. Specific amino-acids in Rubisco are associated with C? photosynthesis in monocots, but it is not known whether selection has acted on Rubisco in a similar way in eudicots.

Methodology/principal findings

We investigated Rubisco evolution in Amaranthaceae sensu lato (including Chenopodiaceae), the third-largest family of C? plants, using phylogeny-based maximum likelihood and Bayesian methods to detect Darwinian selection on the chloroplast rbcL gene in a sample of 179 species. Two Rubisco residues, 281 and 309, were found to be under positive selection in C? Amaranthaceae with multiple parallel replacements of alanine by serine at position 281 and methionine by isoleucine at position 309. Remarkably, both amino-acids have been detected in other C? plant groups, such as C? monocots, illustrating a striking parallelism in molecular evolution.

Conclusions/significance

Our findings illustrate how simple genetic changes can contribute to the evolution of photosynthesis and strengthen the hypothesis that parallel amino-acid replacements are associated with adaptive changes in Rubisco.

SUBMITTER: Kapralov MV 

PROVIDER: S-EPMC3527620 | biostudies-literature | 2012

REPOSITORIES: biostudies-literature