Transient molecular chimerism for exploiting xenogeneic organelles
Yuichiro Kashiyama, Moe Maruyama, Masami Nakazawa, Tsuyoshi Kagamoto, Hiroki Imanishi, Sayaka Yamamoto, Mio Inoue, Ryo Onuma, Goro Tanifuji, Hiroki Ashida, Noriko Inada, Koichiro Awai, Shin-ya Miyagishima

TL;DR
This paper explores how a flagellate uses foreign chloroplasts and its own proteins to support photosynthesis, offering insights into organelle evolution.
Contribution
The study provides the first biochemical evidence of transient molecular chimerism in xenogeneic organelles in eukaryotes.
Findings
Host-encoded proteins are imported into kleptoplasts to support photosynthesis.
Knockdown of RvRbcS-like protein impairs photosynthesis in kleptoplasts.
Protein translocation into kleptoplasts requires new transport systems after each acquisition.
Abstract
The symbiogenetic origin of organelles, such as chloroplasts, is established, and organelle genomes provide evidence of prokaryotic ancestry. Nevertheless, most organelle proteins are nuclear-encoded and function in concert with those expressed from the organelle genomes, representing constitutive molecular chimerism. The evolutionary forces generating chimerism have been widely discussed, but without much evidence. Here we provide biochemical evidence of transient molecular chimerism in nature, along with a possible mechanistic explanation for chimerism. In the flagellate, Rapaza viridis, nuclear-encoded proteins support photosynthesis in transient, xenogeneic chloroplasts (kleptoplasts) acquired from the green alga Tetraselmis sp. We focused on two putative kleptoplast-targeted proteins: a RuBisCO small subunit-like protein (RvRbcS-like) and a RuBisCO activase homologue.…
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Taxonomy
TopicsPhotosynthetic Processes and Mechanisms · Protist diversity and phylogeny · Mitochondrial Function and Pathology
