TY - JOUR
T1 - Hierarchal order in the formation of chloroplast division machinery in the red alga Cyanidioschyzon merolae
AU - Sumiya, Nobuko
AU - Miyagishim, Shin ya
N1 - Funding Information:
This study was supported by Japan Society for the Promotion of Science Grant-in-Aid for Scientific Research 25251039 (to S.-y.M.) and by the Core Research for Evolutional Science and Technology Program of the Japan Science and Technology Agency (S.-y.M.).
Publisher Copyright:
© 2017 Nobuko Sumiya and Shin-ya Miyagishima.
PY - 2017/3/4
Y1 - 2017/3/4
N2 - Chloroplasts have evolved from a cyanobacterial endosymbiont and multiply by dividing. Chloroplast division is performed by constriction of the ring-like protein complex (the PD machinery), which forms at the division site. The PD machinery is composed of cyanobacteriadescended components such as FtsZ and eukaryote-derived proteins such as the dynamin-related protein, DRP5B. In the red alga Cyanidioschyzon merolae, FtsZ ring formation on the stromal side precedes PDR1 and DRP5B ring formation on the cytosolic side. In this study, we impaired FtsZ ring formation in C. merolae by overexpressing FtsZ just before FtsZ ring formation. As a result, PDR1 and DRP5B failed to localize at the chloroplast division site, suggesting that FtsZ ring formation is required for the PDR1 and DRP5B rings. We further found, by expressing a dominant negative form of DRP5B, that DRP5B ring formation begins on the nuclear side of the chloroplast division site. These findings provide insight into how the PD machinery forms in red algae.
AB - Chloroplasts have evolved from a cyanobacterial endosymbiont and multiply by dividing. Chloroplast division is performed by constriction of the ring-like protein complex (the PD machinery), which forms at the division site. The PD machinery is composed of cyanobacteriadescended components such as FtsZ and eukaryote-derived proteins such as the dynamin-related protein, DRP5B. In the red alga Cyanidioschyzon merolae, FtsZ ring formation on the stromal side precedes PDR1 and DRP5B ring formation on the cytosolic side. In this study, we impaired FtsZ ring formation in C. merolae by overexpressing FtsZ just before FtsZ ring formation. As a result, PDR1 and DRP5B failed to localize at the chloroplast division site, suggesting that FtsZ ring formation is required for the PDR1 and DRP5B rings. We further found, by expressing a dominant negative form of DRP5B, that DRP5B ring formation begins on the nuclear side of the chloroplast division site. These findings provide insight into how the PD machinery forms in red algae.
KW - Chloroplast division
KW - Cyanidioschyzon merolae
KW - DRP5B
KW - FtsZ
KW - PDR1
KW - Plastid division machinery
UR - http://www.scopus.com/inward/record.url?scp=85035801034&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85035801034&partnerID=8YFLogxK
U2 - 10.1080/19420889.2017.1294298
DO - 10.1080/19420889.2017.1294298
M3 - Article
AN - SCOPUS:85035801034
SN - 1942-0889
VL - 10
JO - Communicative and Integrative Biology
JF - Communicative and Integrative Biology
IS - 2
M1 - e1294298
ER -