Ence data [17]. PZ-51 chemical information Amaranthaceae sensu lato (henceforth referred to as Amaranthaceae) constitutes the most diverse lineage of the Caryophyllales. Both C3 and C4 species from this family are adapted to a range of conditions from temperate meadows to the tropics, hot deserts and salt marshes. However, it has been shown that the abundance of C4 Amaranthaceae is correlated with precipitation but not temperature, in contrast to the abundance of C4 Poaceae and Cyperaceae, which is correlated with temperature but not precipitation [22]. Despite C4 Amaranthaceae showing different suites of anatomical and biochemical adaptations as well as ecological preferences compared to C4 Poaceae and Cyperaceae, like C4 monocots they possess faster but less CO2-specific Rubiscos than their C3 relatives [3,5,23]. Thus, Rubisco of C4 eudicots and monocots represents a notable example of convergent evolution of enzyme properties in phylogenetically distant groups. However, it is not known whether this functional convergence in Rubisco kinetics evolved via similar or different structural changes 15481974 in protein [24]. Molecular adaptation can be inferred from comparison of the rates of nonsynonymous (changing amino-acid protein sequence, dN) and synonymous (resulting in no change at the protein level, dS) mutations along a phylogenetic tree using maximum likelihoodand Bayesian frameworks [25]. Recently, such methodology has been applied to the chloroplast gene rbcL, which encodes the large subunit of Rubisco that forms the enzyme’s active site, and showed that positive Darwinian selection is acting within most lineages of 
plants [6]. Only a small fraction of Rubisco MedChemExpress 298690-60-5 residues appear to be under positive selection, while most residues have been under purifying selection [6]. Some of these residues have been shown to be under positive selection within C4 lineages of Poaceae and Cyperaceae [26] and in the small Asteraceae genus, Flaveria [27], which contains both C3 and C4 species. However, no specific analysis has yet been made of Rubisco sequence evolution in a large group of C4 eudicots. In this study, we investigate positive selection on the rbcL gene of plants from the Amaranthaceae family and, in particular, focus on coevolution of Rubisco and C4 photosynthesis asking whether positive selection on the rbcL gene occured on branches leading to C4 clades and/or within C4 clades. Finally, we address the following question: which amino-acid replacements were associated with transitions from C3 to C4 photosynthesis in Amaranthaceae, and are these replacements unique to this lineage or shared with C4 monocots and/or Flaveria?Materials and Methods Phylogenetic analysisWe obtained all Amaranthaceae rbcL nucleotide sequences available in GenBank and aligned them. Sequences shorter than 1341 base pairs and sequences with missing data were excluded. The resulting trimmed alignment consisted of 179 rbcL sequences of 1341 base pairs long which represented 94 12926553 of the rbcL coding region and corresponded to positions 64 to 1404 of the rbcL sequence of Spinacia oleracea (GenBank AJ400848). The analysed dataset consisted of 95 C3 and 84 C4 species (Table S1). Most of the included sequences came from four studies [19,28,29,30] and evenly represented all main lineages within the family (Fig. 1). Phylogeny was reconstructed using a maximum-likelihood inference (ML) conducted with RAxML version 7.2.6 [31] using the raxmlGUI interface [32]. We conducted five independent runs from different s.Ence data [17]. Amaranthaceae sensu lato (henceforth referred to as Amaranthaceae) constitutes the most diverse lineage of the Caryophyllales. Both C3 and C4 species from this family are adapted to a range of conditions from temperate meadows to the tropics, hot deserts and salt marshes. However, it has been shown that the abundance of C4 Amaranthaceae is correlated with precipitation but not temperature, in contrast to the abundance of C4 Poaceae and Cyperaceae, which is correlated with temperature but not precipitation [22]. Despite C4 Amaranthaceae showing different suites of anatomical and biochemical adaptations as well as ecological preferences compared to C4 Poaceae and Cyperaceae, like C4 monocots they possess faster but less CO2-specific Rubiscos than their C3 relatives [3,5,23]. Thus, Rubisco of C4 eudicots and monocots represents a notable example of convergent evolution of enzyme properties in phylogenetically distant groups. However, it is not known whether this functional convergence in Rubisco kinetics evolved via similar or different structural changes 15481974 in protein [24]. Molecular adaptation can be inferred from comparison 
of the rates of nonsynonymous (changing amino-acid protein sequence, dN) and synonymous (resulting in no change at the protein level, dS) mutations along a phylogenetic tree using maximum likelihoodand Bayesian frameworks [25]. Recently, such methodology has been applied to the chloroplast gene rbcL, which encodes the large subunit of Rubisco that forms the enzyme’s active site, and showed that positive Darwinian selection is acting within most lineages of plants [6]. Only a small fraction of Rubisco residues appear to be under positive selection, while most residues have been under purifying selection [6]. Some of these residues have been shown to be under positive selection within C4 lineages of Poaceae and Cyperaceae [26] and in the small Asteraceae genus, Flaveria [27], which contains both C3 and C4 species. However, no specific analysis has yet been made of Rubisco sequence evolution in a large group of C4 eudicots. In this study, we investigate positive selection on the rbcL gene of plants from the Amaranthaceae family and, in particular, focus on coevolution of Rubisco and C4 photosynthesis asking whether positive selection on the rbcL gene occured on branches leading to C4 clades and/or within C4 clades. Finally, we address the following question: which amino-acid replacements were associated with transitions from C3 to C4 photosynthesis in Amaranthaceae, and are these replacements unique to this lineage or shared with C4 monocots and/or Flaveria?Materials and Methods Phylogenetic analysisWe obtained all Amaranthaceae rbcL nucleotide sequences available in GenBank and aligned them. Sequences shorter than 1341 base pairs and sequences with missing data were excluded. The resulting trimmed alignment consisted of 179 rbcL sequences of 1341 base pairs long which represented 94 12926553 of the rbcL coding region and corresponded to positions 64 to 1404 of the rbcL sequence of Spinacia oleracea (GenBank AJ400848). The analysed dataset consisted of 95 C3 and 84 C4 species (Table S1). Most of the included sequences came from four studies [19,28,29,30] and evenly represented all main lineages within the family (Fig. 1). Phylogeny was reconstructed using a maximum-likelihood inference (ML) conducted with RAxML version 7.2.6 [31] using the raxmlGUI interface [32]. We conducted five independent runs from different s.
