Ultrastructural Changes in Shoot Apical Meristem of Canola (Brassica napus cv. Symbol) Treated with Sodium Chloride

2008 ◽  
Vol 11 (8) ◽  
pp. 1161-1164 ◽  
Author(s):  
Homa Mahmoodzad
2006 ◽  
Vol 84 (3) ◽  
pp. 371-383 ◽  
Author(s):  
Nicole S. Ramesar-Fortner ◽  
Edward C. Yeung

The effect of auxins and abscisic acid (ABA) on shoot apical meristem development and function was analyzed in microspore-derived embryos of Brassica napus L. ‘Topas’. Embryos were treated with an auxin transport inhibitor, tri-iodobenzoic acid (TIBA) or exogenous indole-3-acetic acid (IAA) at various stages during their development. If embryos were treated at the preglobular or globular stages of embryogenesis, they developed one fused cotyledon indicating a continuation of radial symmetry. However, if treated later in development, embryos were comparable to the control and formed two separate cotyledons. To demonstrate that this was not a pharmacological effect, an auxin antagonist, 2-(p-chlorophenoxy)-2-methylpropionic acid, included with the TIBA treatment produced normal embryos with two separate cotyledons. Histological observations revealed that the shoot apical meristem of the embryos treated with TIBA or IAA at the preglobular and globular stages was altered. Preglobular and globular stage embryos that were treated with TIBA exhibited a dramatic decline in conversion frequency compared with their controls. Embryos that were treated later in development had conversion frequencies comparable to their controls, and their shoot apical meristems also were similar to controls. Application of ABA at the preglobular and globular stages maintained meristem integrity and improved embryo conversion. However, ABA could not reverse the TIBA effect.


Development ◽  
1991 ◽  
Vol 111 (2) ◽  
pp. 299-313 ◽  
Author(s):  
D.E. Fernandez ◽  
F.R. Turner ◽  
M.L. Crouch

Probes derived from cDNA clones of napin and cruciferin, the major storage proteins of Brassica napus, and in situ hybridization techniques were used to examine changes in the spatial and temporal distribution of storage protein messages during the course of embryogeny, with a special emphasis on the developing apical meristems. Napin mRNAs begin to accumulate in the cortex of the axis during late heart stage, in the outer faces of the cotyledons during torpedo stage and in the inner faces of the cotyledons during cotyledon stage. Cruciferin mRNAs accumulate in a similar pattern but approximately 5 days later. Cells in the apical regions where root and shoot meristems develop do not accumulate storage protein messages during early stages of embryogeny. In the upper axis, the boundary between these apical cells and immediately adjacent cells that accumulate napin and cruciferin mRNAs is particularly distinct. Our analysis indicates that this boundary is not related to differences in tissue or cell type, but appears instead to be coincident with the site of a particular set of early cell divisions. A major change in the mRNA accumulation patterns occurs halfway through embryogeny, as the embryos enter maturation stage and start drying down. Final maturation of the shoot apical meristem is associated with the development of leaf primordia and the accumulation of napin mRNAs in the meristem, associated leaf primordia and vascular tissue. Cruciferin mRNAs accumulate only in certain zones of the shoot apical meristem and on the flanks of leaf primordia. Neither type of mRNA accumulates in the root apical meristem at any stage.


2001 ◽  
Vol 79 (3) ◽  
pp. 265-273
Author(s):  
Nicole S Ramesar-Fortner ◽  
Edward C Yeung

The effect of an auxin transport inhibitor, tri-iodobenzoic acid, on the formation and subsequent function of the shoot apical meristem in zygotic embryos of Brassica napus L. was examined. Globular and heart stage embryos were cultured in the presence of tri-iodobenzoic acid. Only embryos at the globular stage of embryogenesis were affected by tri-iodobenzoic acid. Upon treatment, the embryos did not develop two separate cotyledons and, therefore, did not attain bilateral symmetry. Furthermore, the shoot apical meristem of these embryos was altered, as a characteristic tunica-corpus organization was not observed. The cells of the surface layer continued to maintain their meristematic characteristics and divided mainly in the anticlinal direction. The subapical cells differentiated into parenchyma cells and continued to expand such that a corpus organization never developed. Therefore, by the end of the culture period, the shoot apical meristem appeared very broad and shallow. Treated embryos that were transferred to a conversion medium exhibited a dramatic decline and delay in the formation of leaves compared with untreated embryos. Histological observations revealed that the shoot apical meristem continued to expand in width. A low percentage of treated embryos were able to convert; however, leaves were produced from a new shoot meristem that developed in the axillary position. No morphological or histological changes were evident when the embryos were treated later, at the heart stage of embryogenesis.Key words: auxin, Brassica napus, embryo, shoot apical meristem, tri-iodobenzoic acid.


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