Baskin T. I., Cork A., Williamson R. E., Gorst J. R.
Plant Cell Biology Group, Research School of Biological Sciences, Australian National University Canberra, Australian Capital Territory 2601, Australia (T.I.B., A.C., R.E.W.).
Plant Physiol. 1995 Jan;107(1):233-243. doi: 10.1104/pp.107.1.233.
To understand the control of spatial patterns of expansion, we have studied root growth in wild type and in the stunted plant 1 mutant, stp1, of Arabidopsis thaliana. We measured profiles of cell length and calculated the distribution of elongation rate. Slow growth of stp1 results both from a failure of dividing cell number to increase and from low elongation rates in the zone of rapid expansion. However, elongation of dividing cells was not greatly affected, and stp1 and wild-type callus grew at identical rates. Thus, rapid cellular expansion differs in mechanism from expansion in dividing cells and is facilitated by the STP1 gene. Additionally, there was no difference between stp1 and wild-type roots for elongation in response to abscisic acid, auxin, ethylene, or gibberellic acid or for radial expansion in response to ethylene; however, stp1 responded to cytokinin much less than wild type. In contrast, both genotypes responded comparably to hormones when explants were cultured; in particular, there was no difference between genotypes in shoot regeneration in response to cytokinin. Thus, effects on root expansion mediated by cytokinin, but not effects mediated by other hormones or effects on other cytokinin-mediated responses, require the STP1 locus.
为了解扩张空间模式的调控机制,我们研究了拟南芥野生型和矮化植株1突变体stp1的根生长情况。我们测量了细胞长度分布并计算了伸长率分布。stp1生长缓慢是由于分裂细胞数量未能增加以及快速扩张区域的伸长率较低。然而,分裂细胞的伸长并未受到太大影响,并且stp1和野生型愈伤组织的生长速率相同。因此,快速的细胞扩张在机制上不同于分裂细胞的扩张,并且受STP1基因促进。此外,在对脱落酸、生长素、乙烯或赤霉素的伸长反应方面,以及对乙烯的径向扩张反应方面,stp1和野生型根之间没有差异;然而,stp1对细胞分裂素的反应远低于野生型。相比之下,当外植体进行培养时,两种基因型对激素的反应相当;特别是,在对细胞分裂素的芽再生反应方面,基因型之间没有差异。因此,细胞分裂素介导的对根扩张的影响,而非其他激素介导的影响或对其他细胞分裂素介导反应的影响,需要STP1基因座。