The DOI matches its Crossref record; 205 of the 208 references it cites were found in a registry or an index.
Evolutionary adaptation of plant annexins has diversified their molecular structures, interactions and functional roles
Open accessAbstract
Summary: Annexins are an homologous, structurally related superfamily of proteins known to associate with membrane lipid and cytoskeletal components. Their involvement in membrane organization, vesicle trafficking and signaling is fundamental to cellular processes such as growth, differentiation, secretion and repair. Annexins exist in some prokaryotes and all eukaryotic phyla within which plant annexins represent a monophyletic clade of homologs descended from green algae. Genomic, proteomic and transcriptomic approaches have provided data on the diversity, cellular localization and expression patterns of different plant annexins. The availability of 35 complete plant genomes has enabled systematic comparative analysis to determine phylogenetic relationships, characterize structures and observe functional specificity between and within individual subfamilies. Short amino termini and selective erosion of the canonical type 2 calcium coordinating sites in domains 2 and 3 are typical of plant annexins. The convergent evolution of alternate functional motifs such as ‘ KGD ’, redox‐sensitive Cys and hydrophobic Trp/Phe residues argues for their functional relevance and contribution to mechanistic diversity in plant annexins. This review examines recent findings and advances in plant annexin research with special focus on their structural diversity, cellular and molecular interactions and their potential integrated functions in the broader context of physiological responses. Contents Summary 695 I. Introduction 695 II. Structural analyses 696 III. Membrane‐related functions 702 IV. Enzyme‐related functions 703 V. Functional insights from proteome and transcriptome analyses 704 VI. Future perspectives 706 Acknowledgements 708 References 708
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“This unusual feature has previously been observed in alpha-giardins and plant annexins (18).”
From Comparative Cell Biology and Evolution of Annexins in Diplomonads (2016) · cites this paper as [18]
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Items 201–205 of 205
Functional identification of α1-giardin as an annexin of Giardia lamblia
Bauer, B. (1999) · FEMS Microbiology Letters · doi:10.1016/s0378-1097(99)00064-6 · Cited by 2
Cloning and Sequencing the Full-length cDNA of Annexin from Strawberry Fruit
Wang, G., Huai-yi, Y., Ran, X., Fang, H., & Shi-Xi, J. (2001) · Journal of Integrative Plant Biology · Cited by 2
The Nucleotide Face of Annexins
Bandorowicz‐Pikuła, J. (2003) · Molecular biology intelligence unit · doi:10.1007/978-1-4419-9214-7_16 · Cited by 2
Wang, Q., Jianli, S., Bao, L., Lian, J., & Huixian, Z. (2011) · AFRICAN JOURNAL OF BIOTECHNOLOGY · doi:10.5897/ajb11.1276 · Cited by 1
Insight into plant annexin function: from shoot to root signaling
Baucher, M., Pérez-Morga, D. L., & Jaziri, M. E. (2012) · Dépôt institutionnel de l'Université libre de Bruxelles (Université Libre de Bruxelles) · Cited by 1
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- 10.1111/j.1365-313X.1993.00763.x · DOI
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Annexin A2 Heterotetramer: Structure and Function
Bharadwaj, A. G., Bydoun, M., Holloway, R. W., & Waisman, D. M. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms14036259 · Cited by 307
Ca2+ signals in plant immunity
Köster, P., DeFalco, T. A., & Zipfel, C. (2022) · The EMBO Journal · doi:10.15252/embj.2022110741 · Cited by 264
Ma, L., Ye, J., Yang, Y., Lin, H., Yue, L., Luo, J., Long, Y., Fu, H., Liu, X., Zhang, Y., et al. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.02.010 · Cited by 239
Annexin-Phospholipid Interactions. Functional Implications
Lizarbe, M., Barrasa, J., Olmo, N., Gavilanes, F., & Turnay, J. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms14022652 · Cited by 234
Hawkesford, M. J., Çakmak, İ., Coskun, D., Kok, L. J. D., Lambers, H., Schjoerring, J. K., & White, P. J. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-819773-8.00019-8 · Cited by 256
Metadata
- Authors
- Clark, G. B., Morgan, R. O., Fernandez, M., & Roux, S. J.
- Affiliations
- The University of Texas at Austin (US)
- Universidad de Oviedo (ES)
- Department of Biochemistry and Molecular Biology Faculty of Medicine and University Institute of Biotechnology of Asturias University of Oviedo E‐33006 Oviedo Spain
- Corresponding author
- Roux, Stanley J.
- Venue
- New Phytologist
- Publisher
- Wiley
- Published
- 2012-09-19
- Volume
- 196
- Issue
- 3
- Pages
- 695-712
- ISSN
- 0028-646X (ISSN-L)
- 1469-8137
- OpenAlex
- W2060477111
- Cited by
- 150
- References
- 208
- Citations by year
- 2026: 4 · 2025: 5 · 2024: 8 · 2023: 11 · 2022: 10 · 2021: 27 · 2020: 13 · 2019: 18 · 2018: 10 · 2017: 7 · 2016: 7 · 2015: 13 · 2014: 7 · 2013: 10
- FWCI
- 0.88
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Licence
- Locations
- New Phytologist (publishedVersion)
- PubMed (publishedVersion)
- Consultation of the Doctoral Thesis Database (TESEO) (Ministerio de Educación, Cultura y Deporte) (submittedVersion, cc-by-nc-nd)
- Funders
- Ministerio de Ciencia e Innovación
- National Science Foundation (0718890, 1027514)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › S100 Proteins and Annexins
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Keywords
- adaptive evolution, phylogenetic relationships, calcium binding sites, membrane organization, vesicle trafficking, cytoskeletal interactions, plant genome
- MeSH terms
- Adaptation, Physiological, Cell Membrane, Markov Chains, Phylogeny, Plant Proteins, Plants, Species Specificity, Structure-Activity Relationship, Genetic Variation, Annexins, Evolution, Molecular, Proteome, Amino Acid Motifs, Gene Expression Profiling, Protein Interaction Mapping
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