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The high expression of TaPDIL2-1, detected not only during shoots development but also in developing spikes and caryopses of wheat, seems congruent with its metabolic role, since active starch synthesis takes place in all these tissues.
A high percentage of budburst does not necessarily lead to a high percentage of fruit-bearing shoots development.
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In tissue culture high auxin and low cytokinin give rise to root development; low auxin and high cytokinin encourage shoot development.
To help understand the differentiation mechanism, shoot development was studied over time in both shoot phases.
Shoot development was enhanced by 10 μM BAP and 10 μM AgNO3 leading to 100% well developed shoots.
Several studies have reported the positive effect of HS on crop yield [19-21] [19-21]root and shont development [6,22].
The greater the number of roots produced by a petiole, the greater the likelihood of shoot development on that petiole.
Little is known about quantitative trait loci (QTLs) and their genetic interaction (epistasis) in lateral shoot development.
The promotion of lateral shoot development by these two florigen genes is independent of their effect on the floral transition of the primary shoot (Hiraoka et al. 2013).
These findings indicate that these flowering genes also regulate other aspects of shoot development and may be used to study the mechanism of shoot growth pattern.
In addition, two florigen genes, FT and TSF, play important roles in linking the floral transition and lateral shoot development to maximize the reproductive success of Arabidopsis plants.
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