TY - JOUR
T1 - Arabidopsis vegetative actin isoforms, AtACT2 and AtACT7, generate distinct filament arrays in living plant cells
AU - Kijima, Saku T.
AU - Staiger, Christopher J.
AU - Katoh, Kaoru
AU - Nagasaki, Akira
AU - Ito, Kohji
AU - Uyeda, Taro Q.P.
N1 - Funding Information:
We wish to thank Dr. S. Kong (Kongju National University) for two kind gifts (vector plasmid and cDNA); Dr. W. Zhang (Purdue University) for teaching the Agroinfiltration method; Dr. M. Wada (Tokyo Metropolitan University) for advice on the observation methods for cp-actin; Dr. N. Mitsuda, Ms. Y. Sugimoto and Ms. M. Yamada (National Institute of Advanced Industrial Science and Technology) for preparation of plant materials; Mr. Y. Hayakawa (Waseda University) for assistance with FFT analysis. We also thank the Riken Cell Bank for providing the T87 cell line and for holding a workshop about protoplasts (August 2015, Tsukuba). This work was supported by Grants-in-aid from the Ministry of Education, Culture, Sports, Science and Technology to SK (No. 17J00236), KI (Nos. 17K07436 and 26440131), KK (Nos. 17H06417 and 17H06413) and TU (No. 24117008), and Physical Biosciences Program of the Office of Basic Energy Sciences from US Department of Energy to CJS (No. DE-FG02-09ER15526). SK was supported by a SUNBOR SCHOLARSHIP by the Suntory Foundation for Life Sciences.
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Flowering plants express multiple actin isoforms. Previous studies suggest that individual actin isoforms have specific functions; however, the subcellular localization of actin isoforms in plant cells remains obscure. Here, we transiently expressed and observed major Arabidopsis vegetative actin isoforms, AtACT2 and AtACT7, as fluorescent-fusion proteins. By optimizing the linker sequence between fluorescent protein and actin, we succeeded in observing filaments that contained these expressed actin isoforms fused with green fluorescent protein (GFP) in Arabidopsis protoplasts. Different colored fluorescent proteins fused with AtACT2 and AtACT7 and co-expressed in Nicotiana benthamiana mesophyll cells co-polymerized in a segregated manner along filaments. In epidermal cells, surprisingly, AtACT2 and AtACT7 tended to polymerize into different types of filaments. AtACT2 was incorporated into thinner filaments, whereas AtACT7 was incorporated into thick bundles. We conclude that different actin isoforms are capable of constructing unique filament arrays, depending on the cell type or tissue. Interestingly, staining patterns induced by two indirect actin filament probes, Lifeact and mTalin1, were different between filaments containing AtACT2 and those containing AtACT7. We suggest that filaments containing different actin isoforms bind specific actin-binding proteins in vivo, since the two probes comprise actin-binding domains from different actin-binding proteins.
AB - Flowering plants express multiple actin isoforms. Previous studies suggest that individual actin isoforms have specific functions; however, the subcellular localization of actin isoforms in plant cells remains obscure. Here, we transiently expressed and observed major Arabidopsis vegetative actin isoforms, AtACT2 and AtACT7, as fluorescent-fusion proteins. By optimizing the linker sequence between fluorescent protein and actin, we succeeded in observing filaments that contained these expressed actin isoforms fused with green fluorescent protein (GFP) in Arabidopsis protoplasts. Different colored fluorescent proteins fused with AtACT2 and AtACT7 and co-expressed in Nicotiana benthamiana mesophyll cells co-polymerized in a segregated manner along filaments. In epidermal cells, surprisingly, AtACT2 and AtACT7 tended to polymerize into different types of filaments. AtACT2 was incorporated into thinner filaments, whereas AtACT7 was incorporated into thick bundles. We conclude that different actin isoforms are capable of constructing unique filament arrays, depending on the cell type or tissue. Interestingly, staining patterns induced by two indirect actin filament probes, Lifeact and mTalin1, were different between filaments containing AtACT2 and those containing AtACT7. We suggest that filaments containing different actin isoforms bind specific actin-binding proteins in vivo, since the two probes comprise actin-binding domains from different actin-binding proteins.
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U2 - 10.1038/s41598-018-22707-w
DO - 10.1038/s41598-018-22707-w
M3 - Article
C2 - 29531328
AN - SCOPUS:85044225684
SN - 2045-2322
VL - 8
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 4381
ER -