The structure of a 2-MDa chloroplast RNA polymerase reveals unexpected evolutionary complexity
Transcription in chloroplasts depends on the Plastid-Encoded RNA polymerase (PEP), a bacterial-derived enzyme whose catalytic core remains encoded by the highly reduced genome inherited from the cyanobacterial ancestor. In land plants, PEP has roughly doubled in size, expanding into a [~]1 MDa multisubunit machinery through the acquisition of numerous nuclear-encoded subunits. Based on phylogenetic analyses, this added complexity has been widely attributed to the demands of plant terrestrialization. Contrary to this view, we show that in the unicellular green alga Chlamydomonas reinhardtii, PEP assembles into an even larger [~]2 MDa complex containing twelve previously uncharacterized nuclear-encoded subunits (PEPS1-12), representing an RNA polymerase architecture of unprecedented size. A cryo-EM structure at 2.7 [A] resolution reveals that several of these subunits occupy positions analogous to those in land plant PEP, and that metabolic enzyme folds have been repurposed as structural scaffolds stabilizing the highly expanded plastid-encoded core. Despite this, most of the newly identified PEPS subunits lack detectable sequence or structural similarity to their land plant counterparts. These findings demonstrate that PEP complexity is not a hallmark of land plant evolution and may instead reflect, at least in part, the evolutionary entrenchment of additional subunits around an expanded plastid-encoded core. More broadly, they suggest that essential organellar machines can acquire substantial structural complexity that leaves little trace in sequence-based analyses, a pattern consistent with constructive neutral evolution.