Chloroplast Outer Envelope Protein CHUP1 Is Essential for Chloroplast Anchorage to the Plasma Membrane and Chloroplast Movement
Open accessAbstract
Chloroplasts change their intracellular distribution in response to light intensity. Previously, we isolated the chloroplast unusual positioning1 (chup1) mutant of Arabidopsis (Arabidopsis thaliana). This mutant is defective in normal chloroplast relocation movement and shows aggregation of chloroplasts at the bottom of palisade mesophyll cells. The isolated gene encodes a protein with an actin-binding motif. Here, we used biochemical analyses to determine the subcellular localization of full-length CHUP1 on the chloroplast outer envelope. A CHUP1-green fluorescent protein (GFP) fusion, which was detected at the outermost part of mesophyll cell chloroplasts, complemented the chup1 phenotype, but GFP-CHUP1, which was localized mainly in the cytosol, did not. Overexpression of the N-terminal hydrophobic region (NtHR) of CHUP1 fused with GFP (NtHR-GFP) induced a chup1-like phenotype, indicating a dominant-negative effect on chloroplast relocation movement. A similar pattern was found in chloroplast OUTER ENVELOPE PROTEIN7 (OEP7)-GFP transformants, and a protein containing OEP7 in place of NtHR complemented the mutant phenotype. Physiological analyses of transgenic Arabidopsis plants expressing truncated CHUP1 in a chup1 mutant background and cytoskeletal inhibitor experiments showed that the coiled-coil region of CHUP1 anchors chloroplasts firmly on the plasma membrane, consistent with the localization of coiled-coil GFP on the plasma membrane. Thus, CHUP1 localization on chloroplasts, with the N terminus inserted into the chloroplast outer envelope and the C terminus facing the cytosol, is essential for CHUP1 function, and the coiled-coil region of CHUP1 prevents chloroplast aggregation and participates in chloroplast relocation movement.
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The hydrophobic section of CHUP1 binds to the chloroplast outer membrane and can connect the chloroplast to the coiled-coil region of the plasma membrane, F-actin binding site, and C-terminal conserved region.
“The hydrophobic section of CHUP1 protein binds to the chloroplast outer membrane, which can connect the chloroplast to the coiled-coil region of the plasma membrane, F-actin binding site, and C-terminal conserved region”
From The action of enhancing weak light capture via phototropic growth and chloroplast movement in plants (2022) · cites this paper as Oikawa et al., 2008
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References 57 · Cited by 181
- Authors
- Oikawa, K., Yamasato, A., Kong, S.-G., Kasahara, M., Nakai, M., Takahashi, F., Ogura, Y., Kagawa, T., & Wada, M.
- Affiliations
- Ritsumeikan University (JP)
- Venue
- Plant Physiology
- Publisher
- Oxford University Press (OUP)
- Published
- 2008-08-20
- Volume
- 148
- Issue
- 2
- Pages
- 829-842
- ISSN
- 0032-0889 (ISSN-L)
- 1532-2548
- PMC
- PMC2556824
- OpenAlex
- W2143873944
- Cited by
- 181
- References
- 57
- Citations by year
- 2026: 6 · 2025: 8 · 2024: 6 · 2023: 14 · 2022: 16 · 2021: 13 · 2020: 8 · 2019: 6 · 2018: 15 · 2017: 6 · 2016: 13 · 2015: 8 · 2014: 10 · 2013: 7 · 2012: 10
- FWCI
- 4.80
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- PLANT PHYSIOLOGY (publishedVersion, cc-by)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Society for the Promotion of Science (20227001)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Light effects on plants
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Keywords
- chloroplast outer envelope, chloroplast positioning, coiled-coil proteins, actin-binding proteins, Arabidopsis thaliana, palisade mesophyll, dominant negative effect, cytoskeleton, subcellular localization
- MeSH terms
- Amino Acid Sequence, Chloroplasts, Membrane Proteins, Microfilament Proteins, Molecular Sequence Data, Mutation, Phenotype, Plasmids, Recombinant Fusion Proteins, RNA, Messenger, Transformation, Genetic, Sequence Alignment, Arabidopsis, DNA, Complementary, Plant Leaves, RNA, Plant, Arabidopsis Proteins, Plants, Genetically Modified, Green Fluorescent Proteins, Chloroplast Proteins
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