Tobacco ringspot virus persists in the shoot apical meristem but not in the root apical meristem of infected tobacco

2009 ◽  
Vol 126 (1) ◽  
pp. 117-122 ◽  
Author(s):  
Fang Dong ◽  
Tomofumi Mochizuki ◽  
Satoshi T. Ohki
Keyword(s):  
Shoot Apical Meristem ◽  
Apical Meristem ◽  
Ringspot Virus ◽  
Root Apical Meristem ◽  
Tobacco Ringspot Virus ◽  
Infected Tobacco

Plant meristems: CLAVATA3/ESR-related signaling in the shoot apical meristem and the root apical meristem

2008 ◽  
Vol 122 (1) ◽  
pp. 31-39 ◽  
Author(s):  
Hiroki Miwa ◽  
Atsuko Kinoshita ◽  
Hiroo Fukuda ◽  
Shinichiro Sawa
Keyword(s):  
Shoot Apical Meristem ◽  
Apical Meristem ◽  
Root Apical Meristem

In situ localization of storage protein mRNAs in developing meristems of Brassica napus embryos

Development ◽  
1991 ◽  
Vol 111 (2) ◽  
pp. 299-313 ◽  
Author(s):  
D.E. Fernandez ◽  
F.R. Turner ◽  
M.L. Crouch
Keyword(s):  
Brassica Napus ◽  
Storage Protein ◽  
Shoot Apical Meristem ◽  
Apical Meristem ◽  
Vascular Tissue ◽  
Leaf Primordia ◽  
Root Apical Meristem ◽  
Cdna Clones ◽  
Final Maturation

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.

scholarly journals The 2b protein of cucumber mosaic virus is essential for viral infection of the shoot apical meristem and for efficient invasion of leaf primordia in infected tobacco plants

2009 ◽  
Vol 90 (12) ◽  
pp. 3015-3021 ◽  
Author(s):  
Anurag Sunpapao ◽  
Takashi Nakai ◽  
Fang Dong ◽  
Tomofumi Mochizuki ◽  
Satoshi T. Ohki
Keyword(s):  
Cucumber Mosaic Virus ◽  
Mosaic Virus ◽  
Shoot Apical Meristem ◽  
Rna Silencing ◽  
Apical Meristem ◽  
Leaf Primordia ◽  
Shoot Meristem ◽  
Tobacco Plants ◽  
2B Protein ◽  
Infected Tobacco

It has been reported previously that a 2b protein-defective mutant of the cucumber mosaic virus (CMV) Pepo strain (Δ2b) induces only mild symptoms in systemically infected tobacco plants. To clarify further the role of the 2b protein as an RNA silencing suppressor in mosaic symptom expression during CMV infection, this study monitored the sequential distribution of Δ2b in the shoot meristem and leaf primordia (LP) of inoculated tobacco. Time-course histochemical observations revealed that Δ2b was distributed in the shoot meristem at 7 days post-inoculation (p.i.), but could not invade shoot apical meristem (SAM) and quickly disappeared from the shoot meristem, whereas wild-type (Pepo) transiently appeared in SAM from 4 to 10 days p.i. In LP, Δ2b signals were detected only at 14 and 21 days p.i., whereas dense Pepo signals were observed in LP from 4 to 18 days p.i. Northern blot analysis showed that small interfering RNA (siRNA) derived from Δ2b RNA accumulated earlier in the shoot meristem and LP than that of Pepo. However, a similar amount of siRNA was detected in both Pepo- and Δ2b-infected plants at late time points. Tissue printing analysis of the inoculated leaves indicated that the areas infected by Pepo increased faster than those infected by Δ2b, whereas accumulation of Δ2b in protoplasts was similar to that of Pepo. These findings suggest that the 2b protein of the CMV Pepo strain determines virulence by facilitating the distribution of CMV in the shoot meristem and LP via prevention of RNA silencing and/or acceleration of cell-to-cell movement.

Critical level of radiation damage of root apical meristem and mechanisms for its recovery in Pisum sativum L.

2011 ◽  
Vol 45 (1) ◽  
pp. 18-26 ◽  
Author(s):  
E. A. Kravets ◽  
A. N. Mikheev ◽  
L. G. Ovsyannikova ◽  
D. M. Grodzinsky
Keyword(s):  
Pisum Sativum ◽  
Radiation Damage ◽  
Apical Meristem ◽  
Critical Level ◽  
Root Apical Meristem ◽  
Pisum Sativum L

scholarly journals Sound Waves Promote Arabidopsis thaliana Root Growth by Regulating Root Phytohormone Content

2021 ◽  
Vol 22 (11) ◽  
pp. 5739
Author(s):  
Joo Yeol Kim ◽  
Hyo-Jun Lee ◽  
Jin A Kim ◽  
Mi-Jeong Jeong
Keyword(s):  
Arabidopsis Thaliana ◽  
Cell Division ◽  
Root Growth ◽  
Apical Meristem ◽  
Cell Number ◽  
Root Apical Meristem ◽  
Control Group ◽  
Auxin Signaling ◽  
Ethylene Signaling ◽  
Sound Waves

Sound waves affect plants at the biochemical, physical, and genetic levels. However, the mechanisms by which plants respond to sound waves are largely unknown. Therefore, the aim of this study was to examine the effect of sound waves on Arabidopsis thaliana growth. The results of the study showed that Arabidopsis seeds exposed to sound waves (100 and 100 + 9k Hz) for 15 h per day for 3 day had significantly longer root growth than that in the control group. The root length and cell number in the root apical meristem were significantly affected by sound waves. Furthermore, genes involved in cell division were upregulated in seedlings exposed to sound waves. Root development was affected by the concentration and activity of some phytohormones, including cytokinin and auxin. Analysis of the expression levels of genes regulating cytokinin and auxin biosynthesis and signaling showed that cytokinin and ethylene signaling genes were downregulated, while auxin signaling and biosynthesis genes were upregulated in Arabidopsis exposed to sound waves. Additionally, the cytokinin and auxin concentrations of the roots of Arabidopsis plants increased and decreased, respectively, after exposure to sound waves. Our findings suggest that sound waves are potential agricultural tools for improving crop growth performance.

scholarly journals Sample preparation for laser-microdissection of soybean shoot apical meristem

2012 ◽  
Vol 3 (1) ◽  
pp. 3 ◽  
Author(s):  
Chui E. Wong ◽  
Mohan B. Singh ◽  
Prem L. Bhalla
Keyword(s):  
Sample Preparation ◽  
Shoot Apical Meristem ◽  
Apical Meristem ◽  
Laser Microdissection ◽  
Specific Cell ◽  
Legume Crop ◽  
Continuous Formation ◽  
Molecular Events ◽  
Depth Analysis ◽  
Specialized Equipment

The shoot apical meristem houses stem cells responsible for the continuous formation of aerial plant organs including leaves and stems throughout the life of plants. Laser-microdissection in combination with high-throughput technology such as next generation sequencing permits an in-depth analysis of molecular events associated with specific cell type of interest. Sample preparation is the most critical step in ensuring good quality RNA to be extracted from samples following laser-microdissection. Here, we optimized the sample preparation for a major legume crop, soybean. We used Farmer’s solution as a fixative and paraffin as the embedding medium for soybean shoot apical meristem tissue without the use of any specialized equipment. Shorter time for tissue fixation (two days) was found to be critical for the preservation of RNA in soybean shoot apical meristem. We further demonstrated the utility of this method for different tissues derived from soybean and rice. The method outlined here shall facilitate studies on crop plants involving laser-microdissection.

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