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本文引用的文献

1
Multipotent versus differentiated cell fate selection in the developing Drosophila airways.果蝇发育中气道内多能细胞与分化细胞命运的选择
Elife. 2015 Dec 2;4:e09646. doi: 10.7554/eLife.09646.
2
Transient junction anisotropies orient annular cell polarization in the Drosophila airway tubes.瞬态连接各向异性使果蝇气道管中环细胞的极化。
Nat Cell Biol. 2015 Dec;17(12):1569-76. doi: 10.1038/ncb3267. Epub 2015 Nov 9.
3
GRHL2 coordinates regeneration of a polarized mucociliary epithelium from basal stem cells.GRHL2协调基底干细胞再生极化的黏液纤毛上皮。
J Cell Biol. 2015 Nov 9;211(3):669-82. doi: 10.1083/jcb.201506014. Epub 2015 Nov 2.
4
A Grainyhead-Like 2/Ovo-Like 2 Pathway Regulates Renal Epithelial Barrier Function and Lumen Expansion.类颗粒头样蛋白2/类Ovo样蛋白2信号通路调控肾上皮屏障功能及管腔扩张。
J Am Soc Nephrol. 2015 Nov;26(11):2704-15. doi: 10.1681/ASN.2014080759. Epub 2015 Mar 18.
5
The intersection of the extrinsic hedgehog and WNT/wingless signals with the intrinsic Hox code underpins branching pattern and tube shape diversity in the drosophila airways.外在刺猬信号通路和WNT/无翅信号通路与内在Hox编码的交汇,是果蝇气道分支模式和管腔形状多样性的基础。
PLoS Genet. 2015 Jan 23;11(1):e1004929. doi: 10.1371/journal.pgen.1004929. eCollection 2015 Jan.
6
Mapping gene regulatory networks in Drosophila eye development by large-scale transcriptome perturbations and motif inference.通过大规模转录组扰动和基序推断绘制果蝇眼睛发育中的基因调控网络
Cell Rep. 2014 Dec 24;9(6):2290-303. doi: 10.1016/j.celrep.2014.11.038. Epub 2014 Dec 18.
7
A GRHL3-regulated repair pathway suppresses immune-mediated epidermal hyperplasia.一种GRHL3调控的修复途径可抑制免疫介导的表皮增生。
J Clin Invest. 2014 Dec;124(12):5205-18. doi: 10.1172/JCI77138. Epub 2014 Oct 27.
8
Src kinases and ERK activate distinct responses to Stitcher receptor tyrosine kinase signaling during wound healing in Drosophila.Src 激酶和 ERK 在果蝇伤口愈合过程中对 Stitcher 受体酪氨酸激酶信号的不同反应进行激活。
J Cell Sci. 2014 Apr 15;127(Pt 8):1829-39. doi: 10.1242/jcs.143016. Epub 2014 Feb 12.
9
Grainyhead-like 2 (GRHL2) distribution reveals novel pathophysiological differences between human idiopathic pulmonary fibrosis and mouse models of pulmonary fibrosis.颗粒头样蛋白 2(GRHL2)的分布揭示了人类特发性肺纤维化和肺纤维化小鼠模型之间新的病理生理学差异。
Am J Physiol Lung Cell Mol Physiol. 2014 Mar 1;306(5):L405-19. doi: 10.1152/ajplung.00143.2013. Epub 2013 Dec 27.
10
Chitinase 3-like 1 regulates cellular and tissue responses via IL-13 receptor α2.几丁质酶 3 样蛋白 1 通过白介素 13 受体 α2 调节细胞和组织反应。
Cell Rep. 2013 Aug 29;4(4):830-41. doi: 10.1016/j.celrep.2013.07.032. Epub 2013 Aug 22.

全基因组范围内对颗粒头靶标的鉴定揭示了与POU结构域转录因子Vvl的调控相互作用。

Genome-wide identification of Grainy head targets in reveals regulatory interactions with the POU domain transcription factor Vvl.

作者信息

Yao Liqun, Wang Shenqiu, Westholm Jakub O, Dai Qi, Matsuda Ryo, Hosono Chie, Bray Sarah, Lai Eric C, Samakovlis Christos

机构信息

Department of Molecular Biosciences, Wenner-Gren Institute, Stockholm University, S10691, Stockholm, Sweden.

Cancer Biology & Genetics Program, Sloan-Kettering Institute, 1275 York Ave, Box 252, New York, NY 10065, USA.

出版信息

Development. 2017 Sep 1;144(17):3145-3155. doi: 10.1242/dev.143297. Epub 2017 Jul 31.

DOI:10.1242/dev.143297
PMID:28760809
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5627367/
Abstract

Grainy head (Grh) is a conserved transcription factor (TF) controlling epithelial differentiation and regeneration. To elucidate Grh functions we identified embryonic Grh targets by ChIP-seq and gene expression analysis. We show that Grh controls hundreds of target genes. Repression or activation correlates with the distance of Grh-binding sites to the transcription start sites of its targets. Analysis of 54 Grh-responsive enhancers during development and upon wounding suggests cooperation with distinct TFs in different contexts. In the airways, Grh-repressed genes encode key TFs involved in branching and cell differentiation. Reduction of the POU domain TF Ventral veins lacking (Vvl) largely ameliorates the airway morphogenesis defects of mutants. Vvl and Grh proteins additionally interact with each other and regulate a set of common enhancers during epithelial morphogenesis. We conclude that Grh and Vvl participate in a regulatory network controlling epithelial maturation.

摘要

颗粒头(Grh)是一种保守的转录因子(TF),可控制上皮细胞的分化和再生。为了阐明Grh的功能,我们通过染色质免疫沉淀测序(ChIP-seq)和基因表达分析确定了胚胎期Grh的靶标。我们发现Grh可调控数百个靶基因。抑制或激活与其结合位点到靶基因转录起始位点的距离相关。对发育过程中和受伤后54个Grh反应性增强子的分析表明,在不同情况下Grh与不同的转录因子协同作用。在气道中,Grh抑制的基因编码参与分支和细胞分化的关键转录因子。POU结构域转录因子腹侧静脉缺失(Vvl)的减少在很大程度上改善了Grh突变体的气道形态发生缺陷。在上皮形态发生过程中,Vvl和Grh蛋白相互作用,并调控一组共同的增强子。我们得出结论,Grh和Vvl参与了控制上皮成熟的调控网络。