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Slides were hybridized with low molecular weight RNA (LMW-RNA), extracted from six grapevine (V. vinifera L. cv Corvina) tissues: ripening berries (three stages analyzed), roots, leaves and young inflorescences.
Of the previous studies that analyzed roots specifically, none used microarray probe sets representing more than 8,100 of the originally predicted 25,498 genes in the Arabidopsis genome [ 11- 14].
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It was revealed that analyzed root cap cells varied in both the precipitate particle sizes and the amount particles per unit of the cellular area.
As plants may modify root system architecture when growth in suboptimal Pi condition, we analyzed root hairs when osnla1 and WT were grown in Pi-sufficient and -deficient conditions.
In statistical analyses, MRI and EMG were analyzed root by root.
We next analyzed root samples from LA3030 and LA3038 tomato plants using real-time RT-PCR.
To find out whether TIP1 played a dominant role in root hair growth, we applied 2-BP to tip1-4 roots and analyzed root hair morphology.
To test if PRMT4a, together with PRMT4b, were also involved in the regulation of this physiological response, we analyzed root growth, a process affected by high salt concentrations.
Afterwards, they reviewed the results, analyzed root causes of some of the problems identified, and developed an action plan to address gaps in performance.
To contrast the cytokinin induction, we analyzed root and shoot samples of cytokinin-deficient 35S CKX1 expressing seedlings of the same age (named CKX1).
In addition, to understand the molecular mechanisms underlying the adaptation of plants to abiotic stress, we analyzed root DNA methylation after imposing water-shortage stress on whole tomato plants through root drying.
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