Kavanová Monika, Lattanzi Fernando Alfredo, Grimoldi Agustín Alberto, Schnyder Hans
Lehrstuhl für Grünlandlehre, Technische Universität München, D-85350 Freising-Weihenstephan, Germany.
Plant Physiol. 2006 Jun;141(2):766-75. doi: 10.1104/pp.106.079699. Epub 2006 Apr 28.
Leaf growth in monocotyledons results from the flux of newly born cells out of the division zone and into the adjacent elongation-only zone, where cells reach their final length. We used a kinematic method to analyze the effect of phosphorus nutrition status on cell division and elongation parameters in the epidermis of Lolium perenne. Phosphorus deficiency reduced the leaf elongation rate by 39% due to decreases in the cell production rate (-19%) and final cell length (-20%). The former was solely due to a lower average cell division rate (0.028 versus 0.046 cell cell(-1) h(-1)) and, thus, a lengthened average cell cycle duration (25 versus 15 h). The number of division cycles of the initial cell progeny (five to six) and, as a result, the number of meristematic cells (32-64) and division zone length were independent of phosphorus status. Accordingly, low-phosphorus cells maintained meristematic activity longer. Lack of effect of phosphorus deficiency on meristematic cell length implies that a lower division rate was matched to a lower elongation rate. Phosphorus deficiency did not affect the elongation-only zone length, thus leading to longer cell elongation duration (99 versus 75 h). However, the substantially reduced postmitotic average relative elongation rate (0.045 versus 0.064 mm mm(-1) h(-1)) resulted in shorter mature cells. In summary, phosphorus deficiency did not affect the general controls of cell morphogenesis, but, by slowing down the rates of cell division and expansion, it slowed down its pace.
单子叶植物的叶片生长源于新生细胞从分裂区流出并进入相邻的仅进行伸长的区域,在该区域细胞达到其最终长度。我们采用运动学方法分析了磷营养状况对多年生黑麦草表皮细胞分裂和伸长参数的影响。由于细胞产生速率(-19%)和最终细胞长度(-20%)降低,缺磷使叶片伸长速率降低了39%。前者完全是由于平均细胞分裂速率较低(0.028对0.046细胞·细胞⁻¹·小时⁻¹),因此平均细胞周期持续时间延长(25对15小时)。初始细胞后代的分裂周期数(五到六个)以及由此产生的分生细胞数(32 - 64个)和分裂区长度与磷状况无关。因此,低磷条件下的细胞保持分生组织活性的时间更长。缺磷对分生细胞长度没有影响,这意味着较低的分裂速率与较低的伸长速率相匹配。缺磷不影响仅进行伸长的区域长度,从而导致细胞伸长持续时间更长(99对75小时)。然而,有丝分裂后平均相对伸长速率大幅降低(0.045对0.064毫米·毫米⁻¹·小时⁻¹)导致成熟细胞更短。总之,缺磷不影响细胞形态发生的总体控制,但通过减缓细胞分裂和扩展速率,减缓了其进程。