The relationship between growth and pattern formation.

Regeneration (Oxford, England) Pub Date : 2016-04-28 eCollection Date: 2016-04-01 DOI:10.1002/reg2.55
Susan V Bryant, David M Gardiner
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引用次数: 0

Abstract

Successful development depends on the creation of spatial gradients of transcription factors within developing fields, and images of graded distributions of gene products populate the pages of developmental biology journals. Therefore the challenge is to understand how the graded levels of intracellular transcription factors are generated across fields of cells. We propose that transcription factor gradients are generated as a result of an underlying gradient of cell cycle lengths. Very long cell cycles will permit accumulation of a high level of a gene product encoded by a large transcription unit, whereas shorter cell cycles will permit progressively fewer transcripts to be completed due to gating of transcription by the cell cycle. We also propose that the gradients of cell cycle lengths are generated by gradients of extracellular morphogens/growth factors. The model of cell cycle gated transcriptional regulation brings focus back to the functional role of morphogens as cell cycle regulators, and proposes a specific and testable mechanism by which morphogens, in their roles as growth factors (how they were originally discovered), also determine cell fate.

生长与模式形成之间的关系
成功的发育有赖于转录因子在发育区域内空间梯度的形成,而基因产物梯度分布的图像充斥着发育生物学期刊的版面。因此,我们面临的挑战是了解细胞内转录因子的梯度水平是如何在各细胞区域内产生的。我们提出,转录因子梯度的产生是细胞周期长度潜在梯度的结果。较长的细胞周期允许大量转录单位编码的基因产物积累,而较短的细胞周期则由于细胞周期对转录的门控作用,允许完成的转录本逐渐减少。我们还提出,细胞周期长度梯度是由细胞外形态发生因子/生长因子梯度产生的。细胞周期门控转录调控模型使人们重新关注形态发生因子作为细胞周期调控因子的功能作用,并提出了一种特定的、可检验的机制,即形态发生因子作为生长因子(它们最初是如何被发现的),也决定了细胞的命运。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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