A proteomics study of the induction of somatic embryogenesis in Medicago truncatula using 2DE and MALDI-TOF/TOF

2012 ◽  
Vol 146 (2) ◽  
pp. 236-249 ◽  
Author(s):  
André M. Almeida ◽  
José R. Parreira ◽  
Romana Santos ◽  
Ana Sofia Duque ◽  
Rita Francisco ◽  
...  
Plants ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 715
Author(s):  
Aline Kadri ◽  
Ghislaine Grenier De March ◽  
François Guerineau ◽  
Viviane Cosson ◽  
Pascal Ratet

The induction of plant somatic embryogenesis is often a limiting step for plant multiplication and genetic manipulation in numerous crops. It depends on multiple signaling developmental processes involving phytohormones and the induction of specific genes. The WUSCHEL gene (WUS) is required for the production of plant embryogenic stem cells. To explore a different approach to induce somatic embryogenesis, we have investigated the effect of the heterologous ArabidopsisWUS gene overexpression under the control of the jasmonate responsive vsp1 promoter on the morphogenic responses of Medicago truncatula explants. WUS expression in leaf explants increased callogenesis and embryogenesis in the absence of growth regulators. Similarly, WUS expression enhanced the embryogenic potential of hairy root fragments. The WUS gene represents thus a promising tool to develop plant growth regulator-free regeneration systems or to improve regeneration and transformation efficiency in recalcitrant crops.


1999 ◽  
Vol 18 (5) ◽  
pp. 398-405 ◽  
Author(s):  
L. O. das Neves ◽  
S. R. L. Duque ◽  
J. S. de Almeida ◽  
P. S. Fevereiro

1998 ◽  
Vol 46 (1) ◽  
pp. 151 ◽  
Author(s):  
K. E. Nolan ◽  
R. J. Rose

Medicago truncatula (Jemalong 2HA) can be regenerated by somatic embryogenesis utilising 1-naphthalene acetic acid (NAA) and 6-benzylaminopurine (BAP). There is a requirement for both NAA and BAP for callus induction and embryo formation. There is no requirement for a drop in auxin concentration to induce embryos. Abscisic acid (ABA) when present with NAA and BAP during embryo formation at a concentration of 1 µM, increases the number of embryos per callus. The ABA treatment stimulates embryo numbers in both light and darkness. The conversion efficiency of embryo to plant is unchanged irrespective of the presence of ABA during embryo formation, indicating that ABA does not improve the regeneration of the embryos once formed. Importantly, the presence of light in the embryo formation period causes a marked inhibition of embryo conversion.


2019 ◽  
Vol 140 (1) ◽  
pp. 35-48 ◽  
Author(s):  
Anna Orłowska ◽  
Ewa Kępczyńska

Abstract Abiotic stress conditions (e.g., wounding, sterilization) are often together with plant growth regulators (e.g., 2,4-d), considered as one of the most important factors initiating plant somatic embryogenesis (SE). The first goal of this work was to answer whether leaf explants of the Medicago truncatula non-embryogenic (M9) line and its embryogenic variant (M9-10a) respond equally to mechanical and chemical stress by analyzing ROS (reactive oxygen species, e.g., O2•−, H2O2) localization, ROS scavenging enzyme activity and expression of genes encoding these enzymes. In explants of both lines, the stress response induced by wounding and chemical sterilization and the defense reaction during the 1st week of callus growth was similar. These defense mechanisms first involve an increase in SOD and CAT activity, later APX. 2,4-d, present at a low concentration (0.5 µM) during the induction phase (IP), is necessary for embryogenic callus formation and, consequently, for embryo development. This herbicide in higher concentrations causes an increase in O2•− accumulation and in antioxidant enzyme activity; however, it does not block the formation of callus and somatic embryos, though it disturbs these processes. Moreover, inhibition or blocking studied processes by DPI, an inhibitor of NADPH oxidase responsible for the production of O2•− and also lowering the expression of genes encoding the antioxidant enzymes leading to change in their activities, clearly indicate that a certain level of ROS is necessary to induce SE.


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