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Krüppel 样因子 Dar1 限制果蝇肠道干细胞的增殖。

The krüppel-like factor Dar1 restricts the proliferation of Drosophila intestinal stem cells.

机构信息

Key Laboratory of Animal Biotechnology, Ministry of Agriculture, College of Veterinary Medicine, Northwest A&F University, Yangling, China.

College of Life Science and Technology, Gansu Agricultural University, Lanzhou, China.

出版信息

FEBS J. 2018 Nov;285(21):3945-3958. doi: 10.1111/febs.14652. Epub 2018 Sep 25.

Abstract

The krüppel-like factors (KLFs) are a family of transcription factor proteins that regulate a wide range of biological processes. In an RNAi-based screening experiment, we identified dendritic arbor reduction 1 (Dar1), which is a KLF member in Drosophila, that inhibited the proliferation of intestinal stem cells (ISCs). We found suppression of Dar1-activated ISC proliferation; as a consequence, the ISCs and the young differentiated cells were increased. On the other hand, overexpression (OE) of Dar1 inhibited ISC division and blocked the formation of ISC lineages. In order to explore the molecular mechanism of the Dar1 functions, we compared the gene expression profiles of the Dar1 knockdown and Dar1 OE midguts, using the deep RNA sequencing (RNA-Seq) technique. This experiment revealed that Dar1 negatively regulated the expression of several critical cell cycle genes. We further provide evidence that Dar1 has a function upstream of the JAK/STAT signaling pathway, suggesting Dar1 can regulate ISC proliferation through different mechanisms. Consistent with these findings, we discovered that Dar1 was downregulated in the wounded midguts, allowing increased ISC proliferation to promote intestinal repair. Our data suggest that Dar1 is a functional homolog of the mammalian KLF4.

摘要

Krüppel 样因子 (KLFs) 是一类转录因子蛋白家族,它们调节广泛的生物学过程。在基于 RNAi 的筛选实验中,我们鉴定了果蝇中的 KLF 成员树突状枝减少 1 (Dar1),它抑制肠道干细胞 (ISCs) 的增殖。我们发现抑制 Dar1 激活的 ISC 增殖;结果,ISCs 和年轻的分化细胞增加。另一方面,Dar1 的过表达 (OE) 抑制了 ISC 的分裂并阻止了 ISC 谱系的形成。为了探索 Dar1 功能的分子机制,我们使用深度 RNA 测序 (RNA-Seq) 技术比较了 Dar1 敲低和 Dar1 OE 中肠的基因表达谱。该实验表明 Dar1 负调控几个关键细胞周期基因的表达。我们进一步提供证据表明 Dar1 在 JAK/STAT 信号通路的上游发挥作用,表明 Dar1 可以通过不同的机制调节 ISC 增殖。与这些发现一致,我们发现 Dar1 在受伤的中肠中下调,允许增加的 ISC 增殖以促进肠道修复。我们的数据表明,Dar1 是哺乳动物 KLF4 的功能同源物。

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