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转录活性的差异决定了肢体的身份。

Divergent transcriptional activities determine limb identity.

机构信息

Laboratory of Molecular Genetics, Institut de recherches cliniques de Montréal, Montréal, Quebec, Canada H2W 1R7.

出版信息

Nat Commun. 2010 Jul 13;1(4):35. doi: 10.1038/ncomms1036.

Abstract

Limbs develop using a common genetic programme despite widely differing morphologies. This programme is modulated by limb-restricted regulators such as hindlimb (HL) transcription factors Pitx1 and Tbx4 and the forelimb (FL) Tbx5. Both Tbx factors have been implicated in limb patterning and growth, but their relative activities and underlying mechanisms remain unclear. In this paper, we show that Tbx4 and Tbx5 harbour conserved and divergent transcriptional regulatory domains that account for their roles in limb development. In particular, both factors share an activator domain and the ability to stimulate limb growth. However, we find that Tbx4 is the primary effector of HL identity for both skeletal and muscle development; this activity relies on a repressor domain that is inactivated by a human TBX4 small-patella syndrome mutation. We propose that limb identity is largely achieved by default in FL, whereas a specific repressor activity unique to Tbx4 determines HL identity.

摘要

尽管四肢具有广泛不同的形态,但它们的发育都使用一个共同的遗传程序。这个程序由 LIM 区域转录因子 Pitx1 和 Tbx4 等限制在肢体的调节因子以及前肢(FL)Tbx5 进行调节。这两种 Tbx 因子都与肢体模式和生长有关,但它们的相对活性和潜在机制仍不清楚。在本文中,我们表明 Tbx4 和 Tbx5 具有保守和分歧的转录调控结构域,这些结构域解释了它们在肢体发育中的作用。特别是,这两个因素都共享一个激活结构域和刺激肢体生长的能力。然而,我们发现 Tbx4 是 HL 骨骼和肌肉发育的主要效应因子;这种活性依赖于一个抑制结构域,该结构域被人类 TBX4 小髌骨综合征突变失活。我们提出,FL 中的肢体身份主要是通过默认实现的,而 Tbx4 特有的特定抑制活性决定了 HL 身份。

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