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HD-Zip Proteins GL2 and HDG11 Have Redundant Functions in Arabidopsis Trichomes, and GL2 Activates a Positive Feedback Loop via MYB23.
Khosla, Aashima; Paper, Janet M; Boehler, Allison P; Bradley, Amanda M; Neumann, Titus R; Schrick, Kathrin.
Afiliação
  • Khosla A; Division of Biology, Kansas State University, Manhattan, Kansas 66506-4901 Department of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, Kansas 66506-3702.
  • Paper JM; Division of Biology, Kansas State University, Manhattan, Kansas 66506-4901.
  • Boehler AP; Division of Biology, Kansas State University, Manhattan, Kansas 66506-4901.
  • Bradley AM; Division of Biology, Kansas State University, Manhattan, Kansas 66506-4901.
  • Neumann TR; Division of Biology, Kansas State University, Manhattan, Kansas 66506-4901.
  • Schrick K; Division of Biology, Kansas State University, Manhattan, Kansas 66506-4901 Department of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, Kansas 66506-3702 Molecular, Cellular, and Developmental Biology, Kansas State University, Manhattan, Kansas 66506-4901 kschrick@ksu.edu
Plant Cell ; 26(5): 2184-2200, 2014 May.
Article em En | MEDLINE | ID: mdl-24824485
ABSTRACT
The class IV homeodomain leucine zipper transcription factor GLABRA2 (GL2) acts in a complex regulatory circuit that regulates the differentiation of trichomes in Arabidopsis thaliana. We describe a genetic interaction with HOMEODOMAIN GLABROUS11 (HDG11), previously identified as a negative regulator of trichome branching. gl2 hdg11 double mutants display enhanced trichome cell-type differentiation defects. Transgenic expression of HDG11 using the GL2 promoter partially suppresses gl2 trichome phenotypes. Vice versa, expression of GL2 under the control of its native promoter partially complements hdg11 ectopic branching. Since gl2 hdg11 and gl2 myb23 double mutants and the triple mutant display similar trichome differentiation defects, we investigated a connection to the R2R3-MYB transcription factor MYB23. We show that MYB23 transcript levels are significantly reduced in shoots from gl2 mutants and that GL2 can drive the expression of a MYB23-promoter fusion to green fluorescent protein. Yeast one-hybrid, chromatin immunoprecipitation, and in planta reporter gene experiments indicate that an L1-box in the MYB23 promoter acts as a GL2 binding site. Taken together, our findings reveal a functional redundancy between GL2 and HDG11, two homeodomain leucine zipper transcription factors previously thought to mediate opposing functions in trichome morphogenesis. A model is proposed in which GL2 transcript levels are maintained through a positive feedback loop involving GL2 activation of MYB23.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2014 Tipo de documento: Article