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Wnt、Ptk7 和 FGFRL 表达梯度控制扁形动物再生中的躯干位置身份。

Wnt, Ptk7, and FGFRL expression gradients control trunk positional identity in planarian regeneration.

机构信息

Department of Molecular Biosciences, Northwestern University, Evanston, United States.

Robert Lurie Comprehensive Cancer Center, Northwestern University, Evanston, United States.

出版信息

Elife. 2016 Apr 13;5:e12850. doi: 10.7554/eLife.12850.

Abstract

Mechanisms enabling positional identity re-establishment are likely critical for tissue regeneration. Planarians use Wnt/beta-catenin signaling to polarize the termini of their anteroposterior axis, but little is known about how regeneration signaling restores regionalization along body or organ axes. We identify three genes expressed constitutively in overlapping body-wide transcriptional gradients that control trunk-tail positional identity in regeneration. ptk7 encodes a trunk-expressed kinase-dead Wnt co-receptor, wntP-2 encodes a posterior-expressed Wnt ligand, and ndl-3 encodes an anterior-expressed homolog of conserved FGFRL/nou-darake decoy receptors. ptk7 and wntP-2 maintain and allow appropriate regeneration of trunk tissue position independently of canonical Wnt signaling and with suppression of ndl-3 expression in the posterior. These results suggest that restoration of regional identity in regeneration involves the interpretation and re-establishment of axis-wide transcriptional gradients of signaling molecules.

摘要

使位置身份重新确立的机制对于组织再生可能至关重要。扁形动物利用 Wnt/β-连环蛋白信号来极化其前后轴的末端,但对于再生信号如何恢复沿身体或器官轴的区域化,知之甚少。我们鉴定了三个在控制再生中躯干-尾部位置身份的重叠全身转录梯度中持续表达的基因。ptk7 编码一个在躯干中表达的激酶失活的 Wnt 共受体,wntP-2 编码一个在后部表达的 Wnt 配体,ndl-3 编码一个在前部表达的保守 FGFRL/nou-darake 诱饵受体的同源物。ptk7 和 wntP-2 独立于经典 Wnt 信号维持和允许适当的躯干组织位置的再生,并抑制后部的 ndl-3 表达。这些结果表明,再生中区域身份的恢复涉及对信号分子的轴宽转录梯度的解释和重新确立。

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