Dubrovsky J G, Gambetta G A, Hernández-Barrera A, Shishkova S, González I
Departamento de Biología Molecular de Plantas, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Apartado Postal 510-3, 62250 Cuernavaca, Morelos, Mexico.
Ann Bot. 2006 May;97(5):903-15. doi: 10.1093/aob/mcj604. Epub 2006 Jan 3.
The basic regulatory mechanisms that control lateral root (LR) initiation are still poorly understood. An attempt is made to characterize the pattern and timing of LR initiation, to define a developmental window in which LR initiation takes place and to address the question of whether LR initiation is predictable.
The spatial patterning of LRs and LR primordia (LRPs) on cleared root preparations were characterized. New measures of LR and LRP densities (number of LRs and/or LRPs divided by the length of the root portions where they are present) were introduced and illustrate the shortcomings of the more customarily used measure through a comparative analysis of the mutant aux1-7. The enhancer trap line J0121 was used to monitor LR initiation in time-lapse experiments and a plasmolysis-based method was developed to determine the number of pericycle cells between successive LRPs.
LRP initiation occurred strictly acropetally and no de novo initiation events were found between already developed LRs or LRPs. However, LRPs did not become LRs in a similar pattern. The longitudinal spacing of lateral organs was variable and the distance between lateral organs was proportional to the number of cells and the time between initiations of successive LRPs. There was a strong tendency towards alternation in LR initiation between the two pericycle cell files adjacent to the protoxylem poles. LR density increased with time due to the emergence of slowly developing LRPs and appears to be unique for individual Arabidopsis accessions.
In Arabidopsis there is a narrow developmental window for LR initiation, and no specific cell-count or distance-measuring mechanisms have been found that determine the site of successive initiation events. Nevertheless, the branching density and lateral organ density (density of LRs and LRPs) are accession-specific, and based on the latter density the average distance between successive LRs can be predicted.
控制侧根起始的基本调控机制仍未得到充分理解。本研究旨在描述侧根起始的模式和时间,确定侧根起始发生的发育窗口,并探讨侧根起始是否具有可预测性。
对经过清理的根系标本上的侧根和侧根原基的空间模式进行了表征。引入了侧根和侧根原基密度的新测量方法(侧根和/或侧根原基的数量除以其所在根段的长度),并通过对突变体aux1-7的比较分析说明了更常用测量方法的不足之处。利用增强子捕获系J0121在延时实验中监测侧根起始,并开发了一种基于质壁分离的方法来确定连续侧根原基之间的中柱鞘细胞数量。
侧根原基的起始严格向顶发生,在已发育的侧根或侧根原基之间未发现从头起始事件。然而,侧根原基发育成侧根的模式并不相似。侧生器官的纵向间距是可变的,侧生器官之间的距离与细胞数量以及连续侧根原基起始之间的时间成正比。靠近原生木质部极的两个中柱鞘细胞列之间的侧根起始有强烈的交替倾向。由于发育缓慢的侧根原基的出现,侧根密度随时间增加,并且似乎因拟南芥不同生态型而异。
在拟南芥中,侧根起始存在一个狭窄的发育窗口,尚未发现特定的细胞计数或距离测量机制来决定连续起始事件的位点。然而,分支密度和侧生器官密度(侧根和侧根原基的密度)具有生态型特异性,基于后者的密度可以预测连续侧根之间的平均距离。