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Nuclear localization of Arabidopsis HD-Zip IV transcription factor GLABRA2 is driven by importin α.
Ahmad, Bilal; Lerma-Reyes, Ruben; Mukherjee, Thiya; Nguyen, Hieu V; Weber, Audra L; Cummings, Emily E; Schulze, Waltraud X; Comer, Jeffrey R; Schrick, Kathrin.
Afiliación
  • Ahmad B; Division of Biology, Kansas State University, Manhattan, KS 66506, USA.
  • Lerma-Reyes R; Division of Biology, Kansas State University, Manhattan, KS 66506, USA.
  • Mukherjee T; Division of Biology, Kansas State University, Manhattan, KS 66506, USA.
  • Nguyen HV; Donald Danforth Plant Science Center, Olivette, MO 63132, USA.
  • Weber AL; Division of Biology, Kansas State University, Manhattan, KS 66506, USA.
  • Cummings EE; Division of Biology, Kansas State University, Manhattan, KS 66506, USA.
  • Schulze WX; Division of Biology, Kansas State University, Manhattan, KS 66506, USA.
  • Comer JR; Department of Plant Systems Biology, University of Hohenheim, Stuttgart, Germany.
  • Schrick K; Department of Anatomy and Physiology, Kansas State University, Manhattan, KS 66506, USA.
J Exp Bot ; 75(20): 6441-6461, 2024 Oct 30.
Article en En | MEDLINE | ID: mdl-39058342
ABSTRACT
GLABRA2 (GL2), a class IV homeodomain leucine-zipper (HD-Zip IV) transcription factor from Arabidopsis, is a developmental regulator of specialized cell types in the epidermis. GL2 contains a monopartite nuclear localization sequence (NLS) that is conserved in most HD-Zip IV members across the plants. We demonstrate that NLS mutations affect nuclear transport and result in a loss-of-function phenotypes. NLS fusions to enhanced yellow fluorescent protein (EYFP) show that it is sufficient for nuclear localization in roots and trichomes. Despite partial overlap of the NLS with the homeodomain, genetic dissection indicates that nuclear localization and DNA binding are separable functions. Affinity purification of GL2 from plants followed by MS-based proteomics identified importin α (IMPα) isoforms as potential GL2 interactors. NLS structural prediction and molecular docking studies with IMPα-3 revealed major interacting residues. Cytosolic yeast two-hybrid assays and co-immunoprecipitation experiments with recombinant proteins verified NLS-dependent interactions between GL2 and several IMPα isoforms. IMPα triple mutants (impα-1,2,3) exhibit abnormal trichome formation and defects in GL2 nuclear localization in trichomes, consistent with tissue-specific and redundant functions of IMPα isoforms. Taken together, our findings provide mechanistic evidence for IMPα-dependent nuclear localization of GL2 in Arabidopsis, a process that is critical for cell type differentiation of the epidermis.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Núcleo Celular / Arabidopsis / Proteínas de Homeodominio / Alfa Carioferinas / Proteínas de Arabidopsis Idioma: En Revista: J Exp Bot Asunto de la revista: BOTANICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Núcleo Celular / Arabidopsis / Proteínas de Homeodominio / Alfa Carioferinas / Proteínas de Arabidopsis Idioma: En Revista: J Exp Bot Asunto de la revista: BOTANICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos