Ibañes Marta, Kawakami Yasuhiko, Rasskin-Gutman Diego, Izpisúa Belmonte Juan Carlos
Gene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Mol Syst Biol. 2006;2:57. doi: 10.1038/msb4100098. Epub 2006 Oct 17.
Gradient formation is a fundamental patterning mechanism during embryo development, commonly related to secreted proteins that move along an existing field of cells. Here, we mathematically address the feasibility of gradients of mRNAs and non-secreted proteins. We show that these gradients can arise in growing tissues whereby cells dilute and transport their molecular content as they divide and grow, a mechanism we termed 'cell lineage transport.' We provide an experimental test by unveiling a distal-to-proximal gradient of Hoxd13 in the vertebrate developing limb bud driven by cell lineage transport, corroborating our model. Our study indicates that gradients of non-secreted molecules exhibit a power-law profile and can arise for a wide range of biologically relevant parameter values. Dilution and nonlinear growth confer robustness to the spatial gradient under changes in the cell cycle period, but at the expense of sensitivity in the timing of gradient formation. We expect that gradient formation driven by cell lineage transport will provide future insights into understanding the coordination between growth and patterning during embryonic development.
梯度形成是胚胎发育过程中的一种基本模式形成机制,通常与沿着现有细胞场移动的分泌蛋白有关。在此,我们从数学角度探讨了mRNA和非分泌蛋白梯度形成的可行性。我们表明,这些梯度可以在生长组织中出现,即细胞在分裂和生长时稀释并运输其分子内容物,我们将这一机制称为“细胞谱系运输”。我们通过揭示脊椎动物发育中的肢芽中由细胞谱系运输驱动的从远端到近端的Hoxd13梯度进行了实验验证,证实了我们的模型。我们的研究表明,非分泌分子的梯度呈现幂律分布,并且在广泛的生物学相关参数值下都可能出现。稀释和非线性生长使空间梯度在细胞周期时长变化时具有稳健性,但代价是梯度形成时间的敏感性降低。我们预计,由细胞谱系运输驱动的梯度形成将为未来理解胚胎发育过程中生长与模式形成之间的协调提供新的见解。