scholarly journals Extracellular H2O2 Induced by Oligogalacturonides Is Not Involved in the Inhibition of the Auxin-Regulated rolB Gene Expression in Tobacco Leaf Explants

2000 ◽  
Vol 122 (4) ◽  
pp. 1379-1386 ◽  
Author(s):  
Daniela Bellincampi ◽  
Nunzio Dipierro ◽  
Giovanni Salvi ◽  
Felice Cervone ◽  
Giulia De Lorenzo
2011 ◽  
Vol 11 (1) ◽  
pp. 76 ◽  
Author(s):  
Hong Cui ◽  
Song-Tao Zhang ◽  
Hui-Juan Yang ◽  
Hao Ji ◽  
Xiu-Jie Wang

2003 ◽  
Vol 81 (6) ◽  
pp. 611-621 ◽  
Author(s):  
Harbinder S Dhaliwal ◽  
Nicole S Ramesar-Fortner ◽  
Edward C Yeung ◽  
Trevor A Thorpe

Tobacco leaf explants can produce both shoots and roots depending on the phytohormones in the medium. These arise directly via meristemoids (meristematic centers), which form distinct primordia and then organs. In this study it was found that shoot primordia arose from the palisade mesophyll cells at the adaxial surface, while root primordia arose from the rib parenchyma cells, near the existing vascular bundles. In studies on competency and determination, it was found that the tobacco leaf explants required 4–6 days in culture on a shoot-inducing medium (SIM) to become determined for shoot formation, while the explants were competent for rooting at excision and needed only 1 day on the root-inducing medium (RIM) to become determined for root formation. Transfer of explants from SIM or RIM to basal medium (BM without phytohormones) and vice versa supported the above findings. Transfer of explants from SIM to RIM and vice versa, delayed the timing of root and shoot formation, but not the position in the explant from which the organs arose. On transfer from SIM to RIM or vice versa, meristemoids that were already determined for shoot or root formation continued to develop, while those not yet determined were inhibited and (or) reverted to parenchymatous tissue. Thus under our culture conditions meristemoids in tobacco leaf explants are not plastic.Key words: competence, determination, meristemoid plasticity, organogenesis, tobacco.


2010 ◽  
Vol 37 (12) ◽  
pp. 1117 ◽  
Author(s):  
Peta Holmes ◽  
Michael A. Djordjevic ◽  
Nijat Imin

Medicago truncatula Gaertn. can generate roots in vitro through the formation of root stem cells from leaf explants cultured with auxin. To identify key genes involved in the early processes of root initiation, we compared gene expression in root-forming cultures (RFC) enriched for root stem cells with non-root-forming cultures (NRFC) and untreated leaves using the Affymetrix Medicago GeneChip. Comparing RFC (at 1 week, before root primordium formation) to normal leaf tissue, we identified 904 and 993 up- and downregulated probe sets. Comparing RFC and NRFC, we identified 92 and 182 up- and downregulated probe sets. By comparing all the samples we identified a set of 76 and 42 probe sets up- and downregulated that may be crucial to root stem cell formation and subsequent root initiation. Upregulated probe sets in RFC include Arabidopsis orthologs that are involved in root stem cell formation and root initiation. To validate the GeneChip results, quantitative real-time RT–PCR analysis was used to examine the expression of specific up- and downregulated genes, all of which positively correlated with the microarray data. We used bioinformatic tools developed to functionally annotate the Medicago genome array. This showed significant changes in metabolism, signalling and the expression of transcription factors including some with described roles in root organogenesis and other genes not previously linked to this process. This data facilitates the mapping of regulatory and metabolic networks in M. truncatula and provides candidates for further functional analysis of root initiation in vitro and in planta.


2004 ◽  
Vol 40 (2) ◽  
pp. 235-238 ◽  
Author(s):  
Harbinder S. Dhaliwal ◽  
Edward C. Yeung ◽  
Trevor A. Thorpe

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