Genes encoding the photosystem II proteins are under purifying selection: an insight into the early evolution of oxygenic photosynthesis

Photosynth Res. 2022 Sep;153(3):163-175. doi: 10.1007/s11120-022-00917-8. Epub 2022 Jun 1.

Abstract

The molecular evolution concerns coding sequences (CDSs) of genes and may affect the structure and function of proteins. Non-uniform use of synonymous codons during translation, known as codon usage bias (CUB), depends on the balance between mutations bias and natural selection. We estimated different CUB indices, i.e. the effective number of codons (ENC), G + C content in the 3rd codon positions (GC3), and codon adaptation index for CDSs of intrinsic proteins of photosystem II (PSII), such as psbA (D1), psbD (D2), psbB (CP47), psbC (CP43), and CDSs of the extrinsic protein psbO (PsbO). These genes occur in all organisms that perform oxygenic photosynthesis (OP) on Earth: cyanobacteria, algae and plants. Comparatively, a similar analysis of codon bias for CDSs of L and M subunits that constitute the core proteins of the type II reaction centre (RCII) in anoxygenic bacteria was performed. Analysis of CUB indices and determination of the number of synonymous (dS) and nonsynonymous substitutions (dN) in all analysed CDSs indicated that the crucial PSII and RCII proteins were under strong purifying (negative) selection in course of evolution. Purifying selection was also estimated for CDSs of atpA, the α subunit of ATP synthase, an enzyme that was most likely already present in the last universal common ancestor (LUCA). The data obtained point to an ancient origin of OP, even in the earliest stages of the evolution of life on Earth.

Keywords: Arabidopsis; Chloroflexi; Evolution; Natural selection; Proteobacteria.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Codon / genetics
  • Evolution, Molecular
  • Oxygen*
  • Photosynthesis / genetics
  • Photosystem II Protein Complex* / genetics
  • Photosystem II Protein Complex* / metabolism
  • Plants / metabolism
  • Proteins / metabolism

Substances

  • Codon
  • Photosystem II Protein Complex
  • Proteins
  • Adenosine Triphosphate
  • Oxygen