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Of structure and function: The nature of the sonic hedgehog-heparan sulfate proteoglycan interaction.

机译:结构与功能:声波刺猬与硫酸乙酰肝素蛋白聚糖相互作用的性质。

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摘要

Development of complex multicellular organisms relies on highly regulated tissue growth and cell fate specification. One molecule that coordinately performs these functions is Sonic Hedgehog (Shh). Understanding how Shh achieves this requires the dissection of Shh structure, and how this structure relates to biological activities elicited by this morphogen. Within the Shh sequence, the Cardin-Weintraub motif/domain is responsible for interactions with heparan sulfate proteoglycans (HSPGs). Altering this interaction results in functional consequences at cellular, molecular and systems levels. We find abrogation of Shh-HSPG interactions perturbs Shh's mitogenic, but not patterning functions. Also, these interactions influence Shh's localization to mitogenic niches. Shh-HSPG interactions act at the single cell to modulate the duration of signaling, promoting a gene expression program important for mitogenesis. At the molecular level, the complex structures of biological macromolecules encode information that instructs biological responses. Structure-activity relationships for polysaccharides, however, are not yet fully understood. We find Shh-dependent neural precursor proliferation requires a proteoglycan partner, wherein the glycosaminoglycan chain has a non-reducing end 2-O-sulfated iduronic acid residue. This motif localizes Shh at the tissue level and amplifies Shh-dependent signals. At the systems level, in a mouse model, mutations in the Cardin-Weintraub motif have the effect of reducing olfactory bulb size. We asked if these gross changes were accompanied by alterations in the structure of glomeruli, which are anatomical-functional units of the olfactory system. Mutant glomeruli are fewer and larger. Functionally, their olfactory discriminatory ability may be impaired. Given that functions of intrinsic inhibitory circuits are essential for such discrimination, we asked if newly-born neurons of these circuits were affected. Their numbers are reduced during development and throughout life. In juvenile mutants, we see changes in gross and glomerular morphology similar to changes seen in adults, suggesting Shh influences olfactory system development. These studies support an important role for Sonic Hedgehog in the organization and proper functioning of the olfactory system. Taken together, these results demonstrate that Shh's organizational role impacts function at several levels. In addition, we find structural changes in Shh's interacting partner, heparan sulfate proteoglycans, alter encoded information, and subsequently, instructions that direct Shh responses.
机译:复杂的多细胞生物的发展依赖于高度受控的组织生长和细胞命运规范。协调执行这些功能的一种分子是Sonic Hedgehog(Shh)。要了解Shh如何实现这一目标,就需要剖析Shh结构,以及该结构与这种吗啡原引发的生物活性之间的关系。在Shh序列中,Cardin-Weintraub基序/结构域负责与硫酸乙酰肝素蛋白聚糖(HSPG)的相互作用。改变这种相互作用会导致细胞,分子和系统水平的功能性后果。我们发现废除Shh-HSPG相互作用扰乱了Shh的促有丝分裂,但没有构图功能。同样,这些相互作用影响Shh的定位到促有丝分裂的生态位。 Shh-HSPG相互作用作用于单个细胞以调节信号传导的持续时间,从而促进对促有丝分裂重要的基因表达程序。在分子水平上,生物大分子的复杂结构编码指示生物反应的信息。然而,多糖的结构-活性关系尚不完全清楚。我们发现Shh依赖的神经前体增殖需要蛋白聚糖伴侣,其中糖胺聚糖链具有非还原端2-O硫酸化的艾杜糖残基。该基序将Shh定位在组织水平,并放大了Shh依赖性信号。在系统水平上,在小鼠模型中,Cardin-Weintraub基序的突变具有减少嗅球大小的作用。我们询问这些总体变化是否伴随着肾小球结构的改变,肾小球是嗅觉系统的解剖功能单元。突变肾小球越来越少。从功能上讲,它们的嗅觉辨别能力可能会受损。鉴于固有抑制电路的功能对于这种区分至关重要,我们询问这些电路的新生神经元是否受到影响。它们的数量在发育过程中和一生中都减少了。在青少年突变体中,我们看到大体和肾小球形态的变化与成年人中看到的变化相似,这表明Shh影响嗅觉系统的发育。这些研究支持Sonic Hedgehog在嗅觉系统的组织和正常运作中的重要作用。综上,这些结果表明,Shh的组织角色在几个层面上影响着职能。此外,我们发现Shh的相互作用伴侣硫酸乙酰肝素蛋白聚糖的结构发生了变化,改变了编码信息,随后发现了指导Shh反应的指令。

著录项

  • 作者

    Witt, Rochelle Marie.;

  • 作者单位

    Harvard University.;

  • 授予单位 Harvard University.;
  • 学科 Neurobiology.;Biochemistry.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 302 p.
  • 总页数 302
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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