Abstract
The malaria parasite Plasmodium and other apicomplexans such as Toxoplasma evolved from photosynthetic organisms and contain an essential, remnant plastid termed the apicoplast. Transcription of the apicoplast genome is polycistronic with extensive RNA processing. Yet little is known about the mechanism of apicoplast RNA processing. In plants, chloroplast RNA processing is controlled by multiple pentatricopeptide repeat (PPR) proteins. Here, we identify the single apicoplast PPR protein, PPR1. We show that the protein is essential and that it binds to RNA motifs corresponding with previously characterized processing sites. Additionally, PPR1 shields RNA transcripts from ribonuclease degradation. This is the first characterization of a PPR protein from a nonphotosynthetic plastid.
Highlights
The malaria parasite Plasmodium falciparum and related apicomplexan parasites such as Toxoplasma evolved from photosynthetic organisms
We present the characterization of the single apicoplast pentatricopeptide repeat (PPR1) protein, increasing our understanding of essential events in apicoplast RNA biology
We show that it is targeted to the apicoplast in both Plasmodium and Toxoplasma
Summary
The malaria parasite Plasmodium falciparum and related apicomplexan parasites such as Toxoplasma evolved from photosynthetic organisms They contain a remnant plastid known as an apicoplast (Gardner, Williamson, & Wilson, 1991; Howe, 1992; McFadden, Reith, Munholland, & Lang‐Unnasch, 1996). PPR proteins are involved in all aspects of organelle RNA biology, including splicing, editing, transcript stability, and translation They are sequence‐specific RNA‐binding proteins, containing 2–30 tandem repeats, with each repeat comprising a 35‐amino acid motif that folds into a helix‐turn‐helix structure (Manna, 2015; Prikryl, Rojas, Schuster, & Barkan, 2011). This is the first characterization of a PPR protein from a nonphotosynthetic chloroplast and represents a leap forward in our understanding of essential events in apicoplast RNA biology
Published Version (Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.