Endrizzi K, Moussian B, Haecker A, Levin J Z, Laux T
Lehrstuhl für Entwicklungsgenetik, Universität Tübingen, Germany.
Plant J. 1996 Dec;10(6):967-79. doi: 10.1046/j.1365-313x.1996.10060967.x.
The function of the SHOOT MERISTEMLESS (STM) gene in shoot and floral meristems throughout Arabidopsis development has been analyzed. The results show that STM plays a major role in maintaining shoot and floral meristems. In an allelic series of stm mutants the shoot meristem was either reduced or completely absent in mature embryos and mutant seedling cotyledons showed partial fusion, indicating that the STM gene affects embryonic shoot meristem development and spacing of cotyledons. Postembryonically, stm mutants initiated adventitious shoot development at a position corresponding to the shoot meristem in wild-type. Repetitively initiated defective mutant shoot and floral meristems were consumed during primordia formation and typically terminated prematurely in fused ectopic primordia, indicating that STM is required for continuous shoot and floral meristem function. Analogous defects were observed in stm embryonic and postembryonic development suggesting that similar mechanisms are employed in embryonic and postembryonic organ primordia initiation. Allelic combination suggest different thresholds for STM requirement during plant development. STM requirement could not be bypassed by standard growth factor regimes or by shoot regeneration from calli. The results suggest that STM functions by preventing incorporation of cells in the meristem center into differentiating organ primordia and that this role can completely account for all defects observed in stm mutants. Mutations in the WUSCHEL (WUS) and ZWILLE (ZLL) genes result in defective organization and premature termination of shoot meristems. Genetic interactions between STM, WUS and ZLL were analyzed and the results indicate that STM acts upstream of WUS and ZLL. Therefore, while STM appears to function in keeping central meristem cells undifferentiated, WUS and ZLL seem to be subsequently required for proper function of these cells.
研究分析了拟南芥发育过程中,无茎端分生组织(STM)基因在茎端和花分生组织中的功能。结果表明,STM在维持茎端和花分生组织方面起着主要作用。在stm突变体的等位基因系列中,成熟胚中的茎端分生组织要么减少,要么完全缺失,突变幼苗子叶显示部分融合,这表明STM基因影响胚胎茎端分生组织的发育以及子叶的间距。在胚胎后期,stm突变体在与野生型茎端分生组织相对应的位置启动不定芽发育。反复启动的有缺陷的突变体茎端和花分生组织在原基形成过程中被消耗,通常在融合的异位原基中过早终止,这表明STM是茎端和花分生组织持续功能所必需的。在stm胚胎和胚胎后期发育中观察到类似缺陷,表明在胚胎和胚胎后期器官原基起始过程中采用了相似机制。等位基因组合表明植物发育过程中对STM需求的不同阈值。标准生长因子处理或愈伤组织诱导的芽再生均无法绕过对STM的需求。结果表明,STM通过阻止分生组织中心的细胞并入分化的器官原基来发挥作用,并且这一作用可以完全解释在stm突变体中观察到的所有缺陷。WUSCHEL(WUS)和ZWILLE(ZLL)基因的突变导致茎端分生组织组织缺陷和过早终止。分析了STM、WUS和ZLL之间的遗传相互作用,结果表明STM在WUS和ZLL的上游起作用。因此,虽然STM似乎在保持中央分生组织细胞未分化方面发挥作用,但WUS和ZLL似乎随后是这些细胞正常功能所必需的。