Baumgartner Stefan
Department of Experimental Medical Sciences, Lund University, BMC D10, S-22184 Lund, Sweden.
Hereditas. 2018 Sep 11;155:28. doi: 10.1186/s41065-018-0067-3. eCollection 2018.
In this commentary, I will review the latest findings on the Bicoid (Bcd) morphogen in , a paradigm for gradient formation taught to biology students for more than two decades. "Seeing is believing" also summarizes the erroneous steps that were needed to elucidate the mechanisms of gradient formation and the path of movement of Bcd. Initially proclaimed as a dogma in 1988 and later incorporated into the SDD model where the broad diffusion of Bcd throughout the embryo was the predominant step leading to gradient formation, the SDD model was irrefutable for more than two decades until first doubts were raised in 2007 regarding the diffusion properties of Bcd associated with the SDD model. This led to re-thinking of the issue and the definition of a new model, termed the ARTS model which could explain most of the physical constraints that were inherently associated with the SDD model. In the ARTS model, gradient formation is mediated by the mRNA which is redistributed along cortical microtubules to form a mRNA gradient which is translated to form the protein gradient. Contrary to the SDD model, there is no Bcd diffusion from the tip. The ARTS model is also compatible with the observed cortical movement of Bcd. I will critically compare the SDD and the ARTS models as well as other models, analyze the major differences, and highlight the path where Bcd is localized during early nuclear cycles.
在这篇评论中,我将回顾关于形态发生素Bicoid(Bcd)的最新研究结果,Bcd是二十多年来生物学学生所学的梯度形成范例。“眼见为实”也总结了阐明梯度形成机制和Bcd移动路径所需的错误步骤。1988年,SDD模型最初被奉为教条,后来被纳入该模型,其中Bcd在整个胚胎中的广泛扩散是导致梯度形成的主要步骤。在2007年首次对与SDD模型相关的Bcd扩散特性提出质疑之前,SDD模型在二十多年里一直无可辩驳。这导致了对该问题的重新思考以及一个新模型的定义,即ARTS模型,该模型可以解释与SDD模型内在相关的大多数物理限制。在ARTS模型中,梯度形成是由mRNA介导的,mRNA沿着皮质微管重新分布以形成mRNA梯度,该梯度被翻译形成蛋白质梯度。与SDD模型相反,没有Bcd从顶端扩散。ARTS模型也与观察到的Bcd皮质运动相兼容。我将批判性地比较SDD模型和ARTS模型以及其他模型,分析主要差异,并突出Bcd在早期核周期中定位的路径。