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刺猬蛋白通过不同的梯度和信号中继机制,在果蝇腹部组织细胞类型和细胞极性。

Hedgehog acts by distinct gradient and signal relay mechanisms to organise cell type and cell polarity in the Drosophila abdomen.

作者信息

Struhl G, Barbash D A, Lawrence P A

机构信息

Howard Hughes Medical Institute, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.

出版信息

Development. 1997 Jun;124(11):2155-65. doi: 10.1242/dev.124.11.2155.

Abstract

The epidermis of the adult Drosophila abdomen is formed by a chain of anterior (A) and posterior (P) compartments, each segment comprising one A and one P compartment. In the accompanying paper (Struhl et al., 1997), we provide evidence that Hedgehog protein (Hh), being secreted from P compartment cells, organises the pattern and polarity of A compartment cells. Here we test whether Hh acts directly or by a signal relay mechanism. We use mutations in Protein Kinase A (PKA) or smoothened (smo) to activate or to block Hh signal transduction in clones of A compartment cells. For cell type, a scalar property, both manipulations cause strictly autonomous transformations: the cells affected are exactly those and only those that are mutant. Hence, we infer that Hh acts directly on A compartment cells to specify the various types of cuticular structures that they differentiate. By contrast, these same manipulations cause non-autonomous effects on cell polarity, a vectorial property. Consequently, we surmise that Hh influences cell polarity indirectly, possibly by inducing other signalling factors. Finally, we present evidence that Hh does not polarise abdominal cells by utilising either Decapentaplegic (Dpp) or Wingless (Wg), the two morphogens through which Hh acts during limb development. We conclude that, in the abdomen, cell type and cell polarity reflect distinct outputs of Hh signalling and propose that these outputs are controlled by separable gradient and signal relay mechanisms.

摘要

成年果蝇腹部的表皮由一系列前部(A)和后部(P)区域组成,每个体节包含一个A区域和一个P区域。在随附的论文中(Struhl等人,1997年),我们提供了证据表明,从P区域细胞分泌的刺猬蛋白(Hh)组织了A区域细胞的模式和极性。在这里,我们测试Hh是直接起作用还是通过信号中继机制起作用。我们利用蛋白激酶A(PKA)或平滑基因(smo)的突变来激活或阻断A区域细胞克隆中的Hh信号转导。对于细胞类型这一标量属性,两种操作都会导致严格的自主转变:受影响的细胞恰好是那些且只有那些发生突变的细胞。因此,我们推断Hh直接作用于A区域细胞,以指定它们分化出的各种类型的表皮结构。相比之下,这些相同的操作对细胞极性这一矢量属性产生非自主效应。因此,我们推测Hh可能通过诱导其他信号因子间接影响细胞极性。最后,我们提供证据表明,Hh在腹部细胞极化过程中,既不利用在肢体发育过程中Hh发挥作用的两种形态发生素——骨形态发生蛋白(Dpp)或无翅蛋白(Wg)。我们得出结论,在腹部,细胞类型和细胞极性反映了Hh信号传导的不同输出,并提出这些输出受可分离的梯度和信号中继机制控制。

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