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Tbx2 通过直接抑制 Gremlin1 终止发育中的小鼠肢芽中的 Shh/Fgf 信号通路。

Tbx2 terminates shh/fgf signaling in the developing mouse limb bud by direct repression of gremlin1.

机构信息

Institute for Molecular Biology, Medizinische Hochschule Hannover, Hannover, Germany.

出版信息

PLoS Genet. 2013;9(4):e1003467. doi: 10.1371/journal.pgen.1003467. Epub 2013 Apr 25.

Abstract

Vertebrate limb outgrowth is driven by a positive feedback loop that involves Sonic hedgehog (Shh) and Gremlin1 (Grem1) in the posterior limb bud mesenchyme and Fibroblast growth factors (Fgfs) in the overlying epithelium. Proper spatio-temporal control of these signaling activities is required to avoid limb malformations such as polydactyly. Here we show that, in Tbx2-deficient hindlimbs, Shh/Fgf4 signaling is prolonged, resulting in increased limb bud size and duplication of digit 4. In turn, limb-specific Tbx2 overexpression leads to premature termination of this signaling loop with smaller limbs and reduced digit number as phenotypic manifestation. We show that Tbx2 directly represses Grem1 in distal regions of the posterior limb mesenchyme allowing Bone morphogenetic protein (Bmp) signaling to abrogate Fgf4/9/17 expression in the overlying epithelium. Since Tbx2 itself is a target of Bmp signaling, our data identify a growth-inhibiting positive feedback loop (Bmp/Tbx2/Grem1). We propose that proliferative expansion of Tbx2-expressing cells mediates self-termination of limb bud outgrowth due to their refractoriness to Grem1 induction.

摘要

脊椎动物肢体的生长由一个正反馈环驱动,该反馈环涉及后肢芽间质中的 Sonic hedgehog (Shh) 和 Gremlin1 (Grem1),以及覆盖在上皮中的 Fibroblast growth factors (Fgfs)。为了避免肢体畸形,如多指畸形,需要对这些信号活动进行适当的时空控制。在这里,我们表明在 Tbx2 缺陷的后肢中,Shh/Fgf4 信号被延长,导致肢芽增大和数字 4 的重复。反过来,肢体特异性的 Tbx2 过表达导致这个信号环路的过早终止,表现为肢小和数字减少。我们表明,Tbx2 直接在后部肢体间质的远端区域抑制 Grem1,允许骨形态发生蛋白 (Bmp) 信号在覆盖的上皮中消除 Fgf4/9/17 的表达。由于 Tbx2 本身是 Bmp 信号的靶标,我们的数据确定了一个生长抑制的正反馈环(Bmp/Tbx2/Grem1)。我们提出,由于对 Grem1 诱导的抗性,表达 Tbx2 的细胞的增殖扩展介导了肢芽生长的自我终止。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1517/3636256/e0f1de68b5fb/pgen.1003467.g001.jpg

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