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Identifying and characterizing genes that regulate vascular tissue-specific functions

Posted on:2006-10-05Degree:Ph.DType:Thesis
University:Virginia Polytechnic Institute and State UniversityCandidate:Zhao, ChengsongFull Text:PDF
GTID:2453390008953536Subject:Biology
Abstract/Summary:
Vascular tissues provide both the mechanical support to the plant body and the conducting cells for the transport of water, mineral solutes, hormones and other signaling molecules, amino acids, and sugars. To identify genes that may regulate vascular tissue-specific functions, we isolated xylem, phloem-cambium, and nonvascular tissues from the Arabidopsis root-hypocotyl, performed a genome-wide comparative analysis of tissue-specific transcripts using the 24K Affymetrix Arabidopsis ATH1 Genome Array (24K GeneChip), and identified potential genes that are required for xylem and phloem differentiation or tissue-specific functions.; Based on this comparative analysis, two phloem-specific G2-like transcription factors, MYR1{09} and MYR2, and a xylem-specific NAC domain family member, XND1, were selected for further characterization. Under continuous light, myr2 plants flowered early, while myr1 plants did not differ significantly from wild type controls. However, double mutant myr1myr2 plants exhibited a novel phenotype characterized by elongated petioles, semi-erect leaf orientation, and suppression of lateral shoot outgrowth. These characteristics are reminiscent of yucca, a dominant Arabidopsis mutant with elevated levels of free auxin. Preliminary results indicated that like yucca, myr1myr2 plants were more resistant than wt plants to 5-mT, a toxic tryptophan analog, suggesting that MYR1 and MYR2 may be involved in regulating tryptophan-dependent auxin biosynthesis. Overexpression of any one of MYR1 isoforms resulted in a phenotype that in some cases resembled that observed in the double mutant, indicating that the regulation mediated by MYR1 and MYR2 may depend on formation of specific heterodimers consisting of isoforms of MYR1 and/or MYR2, and that the dimerization was susceptible to disruption both by overexpression and loss-of-function of MYR1/MYR2.
Keywords/Search Tags:MYR2, MYR1, Tissue-specific, Genes
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