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本文引用的文献

1
Quantitative analyses of EGFR localization and trafficking dynamics in the follicular epithelium.定量分析滤泡上皮细胞中 EGFR 的定位和运输动态。
Development. 2020 Aug 14;147(15):dev183210. doi: 10.1242/dev.183210.
2
analysis of patterning evolution of the BMP type II receptor Wishful thinking.BMP 型 II 受体 Wishful thinking 模式进化分析。
Development. 2018 Jul 9;145(13):dev161083. doi: 10.1242/dev.161083.
3
Diversification of heart progenitor cells by EGF signaling and differential modulation of ETS protein activity.通过 EGF 信号和 ETS 蛋白活性的差异调节实现心脏祖细胞的多样化。
Elife. 2018 Jun 5;7:e32847. doi: 10.7554/eLife.32847.
4
On the evolution of bilaterality.论双侧性的演化
Development. 2017 Oct 1;144(19):3392-3404. doi: 10.1242/dev.141507.
5
Simple Expression Domains Are Regulated by Discrete CRMs During Oogenesis.在卵子发生过程中,简单表达结构域由离散的顺式调控模块调控。
G3 (Bethesda). 2017 Aug 7;7(8):2705-2718. doi: 10.1534/g3.117.043810.
6
Gene regulation during eggshell patterning.蛋壳图案形成过程中的基因调控。
Proc Natl Acad Sci U S A. 2017 Jun 6;114(23):5808-5813. doi: 10.1073/pnas.1610619114.
7
The repertoire of epithelial morphogenesis on display: Progressive elaboration of Drosophila egg structure.所展示的上皮形态发生的全部过程:果蝇卵结构的逐步精细发育。
Mech Dev. 2017 Dec;148:18-39. doi: 10.1016/j.mod.2017.04.002. Epub 2017 Apr 19.
8
Uncoupling neurogenic gene networks in the embryo.解开胚胎中的神经源性基因网络。
Genes Dev. 2017 Apr 1;31(7):634-638. doi: 10.1101/gad.297150.117. Epub 2017 Apr 20.
9
Determination of EGFR Signaling Output by Opposing Gradients of BMP and JAK/STAT Activity.通过骨形态发生蛋白(BMP)和JAK/STAT活性的相反梯度来确定表皮生长因子受体(EGFR)信号输出
Curr Biol. 2016 Oct 10;26(19):2572-2582. doi: 10.1016/j.cub.2016.07.073. Epub 2016 Sep 1.
10
Phagocytosis genes nonautonomously promote developmental cell death in the Drosophila ovary.吞噬作用基因非自主地促进果蝇卵巢中的发育性细胞死亡。
Proc Natl Acad Sci U S A. 2016 Mar 1;113(9):E1246-55. doi: 10.1073/pnas.1522830113. Epub 2016 Feb 16.

ETS 转录因子 Pointed 足以调节滤泡上皮的后命运。

The ETS-transcription factor Pointed is sufficient to regulate the posterior fate of the follicular epithelium.

机构信息

Center for Computational and Integrative Biology, Rutgers, The State University of NJ, Camden, NJ 08102, USA.

Department of Biology, Rutgers, The State University of NJ, Camden, NJ 08102, USA.

出版信息

Development. 2020 Nov 15;147(22):dev189787. doi: 10.1242/dev.189787.

DOI:10.1242/dev.189787
PMID:33028611
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7687869/
Abstract

The Janus-kinase/signal transducer and activator of transcription (JAK/STAT) pathway regulates the anterior posterior axis of the follicle cells. In the anterior, it activates the bone morphogenetic protein (BMP) signaling pathway through expression of the BMP ligand (). In the posterior, JAK/STAT works with the epidermal growth factor receptor (EGFR) pathway to express the T-box transcription factor (). Although MID is necessary for establishing the posterior fate of the egg chamber, we show that it is not sufficient to determine a posterior fate. The ETS-transcription factor pointed () is expressed in an overlapping domain to in the follicle cells. This study shows that is upstream of and that it is sufficient to induce a posterior fate in the anterior end, which is characterized by the induction of , the prevention of the stretched cells formation and the abrogation of border cell migration. We demonstrate that the anterior BMP signaling is abolished by PNT through repression. However, ectopic DPP cannot rescue the anterior fate formation, suggesting additional targets of PNT participate in the posterior fate determination.

摘要

Janus 激酶/信号转导和转录激活因子(JAK/STAT)通路调节滤泡细胞的前后轴。在前部,通过表达骨形态发生蛋白(BMP)配体()激活 BMP 信号通路。在后部,JAK/STAT 与表皮生长因子受体(EGFR)通路合作表达 T 盒转录因子()。尽管 MID 对于建立卵室的后命运是必需的,但我们表明它不足以确定后命运。ETS 转录因子 pointed()在与滤泡细胞中的 重叠的域中表达。这项研究表明 是 的上游,并且它足以在前部诱导后命运,其特征在于诱导 、阻止伸展细胞形成和消除边缘细胞迁移。我们证明 PNT 通过 抑制来消除前部的 BMP 信号。然而,异位 DPP 不能挽救前部命运形成,这表明 PNT 的其他靶标参与后部命运决定。