Institut de Biologia Molecular de Barcelona and Institute for Research in Biomedicine, 08028 Barcelona, Spain.
Sci Signal. 2010 Aug 24;3(136):ra63. doi: 10.1126/scisignal.2001059.
Morphogens form signaling gradients that control patterning processes during development. Responding cells must perceive and interpret the concentration-dependent information provided by the morphogen to generate precise patterns of gene expression and cell differentiation in developing tissues. Generally, the absolute number of activated, ligand-bound receptors determines cell perception of the morphogen. In contrast, cells interpret the morphogen Hedgehog (Hh) by measuring the ratio of bound to unbound molecules of its receptor Patched (Ptc). This ratio depends on both the Hh concentration and the absolute number of Ptc molecules. Here, I describe a posttranscriptional process that controls the absolute amount of Ptc present in a cell, which regulates gradient interpretation, wherein self-induced receptor down-regulation that is independent of ligand binding dictates the cell response to a morphogen gradient.
形态发生素形成信号梯度,在发育过程中控制着模式形成过程。应答细胞必须感知和解释形态发生素提供的浓度依赖性信息,以在发育组织中产生精确的基因表达和细胞分化模式。通常,激活的、配体结合的受体的绝对数量决定了细胞对形态发生素的感知。相比之下,细胞通过测量其受体 patched (Ptc)的结合分子与未结合分子的比值来解释形态发生素 Hedgehog (Hh)。这个比值取决于 Hh 浓度和 Ptc 分子的绝对数量。在这里,我描述了一个转录后过程,该过程控制着细胞中存在的 Ptc 的绝对数量,从而调节梯度解释,其中受体的自我诱导下调是独立于配体结合的,决定了细胞对形态发生素梯度的反应。