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Multiple Links between HD-Zip Proteins and Hormone Networks.
- Source :
-
International journal of molecular sciences [Int J Mol Sci] 2018 Dec 14; Vol. 19 (12). Date of Electronic Publication: 2018 Dec 14. - Publication Year :
- 2018
-
Abstract
- HD-Zip proteins are unique to plants, and contain a homeodomain closely linked to a leucine zipper motif, which are involved in dimerization and DNA binding. Based on homology in the HD-Zip domain, gene structure and the presence of additional motifs, HD-Zips are divided into four families, HD-Zip I⁻IV. Phylogenetic analysis of HD-Zip genes using transcriptomic and genomic datasets from a wide range of plant species indicate that the HD-Zip protein class was already present in green algae. Later, HD-Zips experienced multiple duplication events that promoted neo- and sub-functionalizations. HD-Zip proteins are known to control key developmental and environmental responses, and a growing body of evidence indicates a strict link between members of the HD-Zip II and III families and the auxin machineries. Interactions of HD-Zip proteins with other hormones such as brassinolide and cytokinin have also been described. More recent data indicate that members of different HD-Zip families are directly involved in the regulation of abscisic acid (ABA) homeostasis and signaling. Considering the fundamental role of specific HD-Zip proteins in the control of key developmental pathways and in the cross-talk between auxin and cytokinin, a relevant role of these factors in adjusting plant growth and development to changing environment is emerging.
- Subjects :
- Algal Proteins genetics
Algal Proteins metabolism
Chlorophyta genetics
Chlorophyta metabolism
Evolution, Molecular
Gene Expression Regulation, Plant
Indoleacetic Acids metabolism
Multigene Family
Phylogeny
Plant Proteins genetics
Plant Proteins metabolism
Homeodomain Proteins genetics
Homeodomain Proteins metabolism
Plant Growth Regulators metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1422-0067
- Volume :
- 19
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- International journal of molecular sciences
- Publication Type :
- Academic Journal
- Accession number :
- 30558150
- Full Text :
- https://doi.org/10.3390/ijms19124047