The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.
Phylogenetic Analysis of the Formin Homology 2 Domain
Open accessAbstract
Formin proteins are key regulators of eukaryotic actin filament assembly and elongation, and many species possess multiple formin isoforms. A nomenclature system based on fundamental features would be desirable, to aid the rapid identification and characterization of novel formins. In this article, we attempt to systematize the formin family by performing phylogenetic analyses of the formin homology 2 (FH2) domain, an independently folding region common to all formins, which alone can influence actin dynamics. Through database searches, we identify 101 FH2 domains from 26 eukaryotic species, including 15 in mice. Sequence alignments reveal a highly conserved yeast-specific insert in the “knob loop” region of the FH2 domain, with unknown functional consequences. Phylogenetic analysis using minimum evolution (ME), maximum parsimony (MP), and maximum likelihood (ML) algorithms strongly supports the existence of seven metazoan groups. Yeast FH2 domains segregate from all other eukaryotes, including metazoans, other fungi, plants, and protists. Sequence comparisons of non-FH2 regions support relationships between three metazoan groups (Dia, DAAM, and FRL) and examine previously identified coiled-coil and Diaphanous auto-regulatory domain sequences. This analysis allows for a formin nomenclature system based on sequence relationships, as well as suggesting strategies for the determination of biochemical and cellular activities of these proteins.
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Cites
The Pfam Protein Families Database
Bateman, A. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.1.276 · Cited by 14,000
PAUP * [Phylogenetic Analysis Using Parsimony (and Other Methods)]
Cummings, M. P. (2004) · Dictionary of Bioinformatics and Computational Biology · doi:10.1002/0471650129.dob0522 · Cited by 5,215
Predicting coiled coils from protein sequences.
Lupas, A., Van Dyke, M., & Stock, J. (1991) · Science · doi:10.1126/science.252.5009.1162 · Cited by 3,953
Molecular Evolution: A Phylogenetic Approach
Page, R., & Holmes, E. C. (1998) · Medical Entomology and Zoology · Cited by 979
Myosins: a diverse superfamily
Sellers, J. R. (2000) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/s0167-4889(00)00005-7 · Cited by 848
The origin and evolution of model organisms
Hedges, S. B. (2002) · Nature Reviews Genetics · doi:10.1038/nrg929 · Cited by 806
Berg, J. S., Powell, B. C., & Cheney, R. E. (2001) · Molecular Biology of the Cell · doi:10.1091/mbc.12.4.780 · Cited by 770
Role of Formins in Actin Assembly: Nucleation and Barbed-End Association
Pruyne, D., Evangelista, M., Yang, C., Bi, E., Zigmond, S., Bretscher, A., & Boone, C. (2002) · Science · doi:10.1126/science.1072309 · Cited by 764
The Pfam Protein Families Database
Bateman, A. G., Birney, E., Cerruti, L., Durbin, R. M., Etwiller, L., Eddy, S. R., Griffiths‐Jones, S., Howe, K., Marshall, M. S., & Sonnhammer, E. L. L. (2002) · PubMed Central · Cited by 764
Bni1p, a Yeast Formin Linking Cdc42p and the Actin Cytoskeleton During Polarized Morphogenesis
Evangelista, M., Blundell, K., Longtine, M. S., Chow, C. J., Adames, N., Pringle, J. R., Peter, M., & Boone, C. (1997) · Science · doi:10.1126/science.276.5309.118 · Cited by 647
Cited by
Actin and Actin-Binding Proteins
Pollard, T. D. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a018226 · Cited by 912
Formin proteins: a domain-based approach
Higgs, H. N. (2005) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2005.04.014 · Cited by 386
Self-citation
Metadata
- Authors
- Higgs, H. N., & Peterson, K. J.
- Venue
- Molecular Biology of the Cell
- Published
- 2005-01
- Volume
- 16
- Issue
- 1
- Pages
- 1-13
- ISSN
- 1059-1524 (ISSN-L)
- 1939-4586
- OpenAlex
- W1972250746
- Cited by
- 278
- References
- 35
- FWCI
- 4.99
- Type
- journal article
- Language
- en
- Open access
- green
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