Tri-iodobenzoic acid affects shoot apical meristem formation and function in zygotic embryos of Brassica napus cv. Topas

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.

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.


Author(s):  
M.D. Sow ◽  
A-L. Le Gac ◽  
R. Fichot ◽  
S. Lanciano ◽  
A. Delaunay ◽  
...  

AbstractAs fixed and long living organisms subjected to repeated environmental stresses, trees have developed mechanisms such as phenotypic plasticity that help them to cope with fluctuating environmental conditions. Here, we tested the role DNA methylation as a hub of integration, linking plasticity and physiological response to water deficit in the shoot apical meristem of the model tree poplar (Populus). Using a reverse genetic approach, we compared hypomethylated RNAi-ddm1 lines to wild-type trees for drought tolerance. An integrative analysis was realized with phytohormone balance, methylomes, transcriptomes and mobilomes.Hypomethylated lines were more tolerant when subjected to moderate water deficit and were intrinsically more tolerant to drought-induced cavitation. The alteration of the DDM1 machinery induced variation in DNA methylation in a cytosine context dependent manner, both in genes and transposable elements. Hypomethylated lines subjected to water deficit showed altered expression of genes involved in phytohormone pathways, such as salicylic acid and modified hormonal balance. Several transposable elements showed stress- and/or line-specific patterns of reactivation, and we could detect copy number variations for two of them in stressed ddm1 lines.Overall, our data highlight two major roles for DNA methylation in the shoot apical meristem: control of stress response and plasticity through transduction of hormone signaling and maintenance of genome integrity through the control of transposable elements.


Development ◽  
1992 ◽  
Vol 116 (2) ◽  
pp. 397-403 ◽  
Author(s):  
H. M. Ottoline Leyser ◽  
I. J. Furner

The shoot apical meristem of dicotyledonous plants is highly regulated both structurally and functionally, but little is known about the mechanisms involved in this regulation. Here we describe the genetic and phenotypic characterisation of recessive mutations at three loci of Arabidopsis thaliana in which meristem structure and function are disrupted. The loci are Clavata1 (Clv1), Fasciata1 (Fas1) and Fasciata2 (Fas2). Plants mutant at these loci are fasciated having broad, flat stems and disrupted phyllotaxy. In all cases, the fasciations are associated with shoot apical meristem enlargement and altered floral development. While all the mutants share some phenotypic features they can be divided into two classes. The pleiotropic fas1 and fas2 mutants are unable to initiate wild- type organs, show major alterations in meristem structure and have reduced root growth. In contrast, clv1 mutant plants show near wild-type organ phenotypes, more subtle changes in shoot apical meristem structure and wild-type root growth.


Agronomy ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 722 ◽  
Author(s):  
Yongpeng Jia ◽  
Kaixiang Li ◽  
Haidong Liu ◽  
Lingxiong Zan ◽  
Dezhi Du

Determinate inflorescences have a significant effect on the genetic improvement of rapeseed, so understanding the molecular function underlying the inflorescence trait may be beneficial to oilseed breeding. A previous study found candidate gene BnTFL1 (Terminal Flower 1) for control of the inflorescence trait on Brassica napus chromosome A10 (16,627–16,847 kb). However, little is known about the function of the BnTFL1 gene in B. napus. In this study, we firstly studied the formation of the shoot apical meristem and gene expression in indeterminate and determinate inflorescences; the results showed that the inflorescence architecture and BnA10.TFL1 expression showed significant differences in the shoot apex at the budding stage. Then, two alleles (named BnA10.TFL1 gene from indeterminate and BnA10.tfl1 gene from determinate) were cloned and sequence-analyzed; the results suggest that the open reading frame of the alleles comprises 537 bp, encodes 178 amino acids containing a conserved phosphatidylethanolamine-binding protein (PEBP) domain, and shares high similarity with Arabidopsis thaliana TFL1. To analyze the function of BnA10.TFL1, the BnA10.TFL1 gene was introduced into the determinate A. thaliana tfl1 mutant and B. napus 571 line by complementation experiment. The determinate traits were restored to indeterminate, and expression of BnA10.TFL1 was increased in the indeterminate shoot apex. These results reveal that BnA10.tfl1 is a gene controlling the determinate inflorescence trait. Moreover, the BnA10.TFL1 protein was localized to the nucleus, cytoplasm, and plasma membrane. Collectively, the results of this study help us to understand the molecular mechanism of determinate inflorescences and will provide a reliable research basis for the application of determinate inflorescences in B. napus.


1992 ◽  
Vol 99 (4) ◽  
pp. 1609-1618 ◽  
Author(s):  
David C. Taylor ◽  
Dennis L. Barton ◽  
Kevin P. Rioux ◽  
Samuel L. MacKenzie ◽  
Darwin W. Reed ◽  
...  

Botany ◽  
2015 ◽  
Vol 93 (7) ◽  
pp. 445-452
Author(s):  
Subramanian Paulraj ◽  
Arturo Lopez-Villalobos ◽  
Edward C. Yeung

The formation of meristemoids and the ontogeny of the shoot apical meristem (SAM) were studied using cultured zygotic embryos of Arabidopsis thaliana (L.) Heynh. LER ecotype. In the callus induction treatment, the procambial cells within the cotyledons of the embryo explants proliferated and gave rise to callus tissues. At the end of the treatment, a band of small cytoplasmic-rich cells derived from the procambium was produced and located at the outer surface of the callus. Upon transfer to the shoot induction medium (SIM) in the absence of abscisic acid (ABA), the cytoplasmic cells differentiated mainly into vascular elements and vacuolated parenchyma cells. This pattern of development negatively affected the explants’ ability to produce meristemoids and SAMs. Contrary to the control, the inclusion of ABA in the SIM resulted first in starch synthesis and accumulation in the surface cytoplasmic cells. This was followed by the formation of cytoplasmic cells among the starch-rich cells; further proliferation of the cytoplasmic cells resulted in the formation of meristemoids. The formation of tracheary elements was suppressed in the ABA-containing SIM. Upon transferring to the shoot development medium, which lacked plant growth regulators, some meristemoids differentiated into apical meristem cells. These cells had distinct nuclei and nucleoli, with little starch present. Additional cell divisions increased the size of the future SAM. Shoot buds with distinct SAMs were clearly delineated with the appearance of leaf primordia.


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