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一个用于合子基因组激活的 FGF 定时器。

An FGF timer for zygotic genome activation.

机构信息

Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey 08544, USA;

Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.

出版信息

Genes Dev. 2023 Feb 1;37(3-4):80-85. doi: 10.1101/gad.350164.122. Epub 2023 Feb 17.

Abstract

Zygotic genome activation has been extensively studied in a variety of systems including flies, frogs, and mammals. However, there is comparatively little known about the precise timing of gene induction during the earliest phases of embryogenesis. Here we used high-resolution in situ detection methods, along with genetic and experimental manipulations, to study the timing of zygotic activation in the simple model chordate with minute-scale temporal precision. We found that two homologs in are the earliest genes that respond to FGF signaling. We present evidence for a FGF timing mechanism that is driven by ERK-mediated derepression of the ERF repressor. Depletion of ERF results in ectopic activation of FGF target genes throughout the embryo. A highlight of this timer is the sharp transition in FGF responsiveness between the eight- and 16-cell stages of development. We propose that this timer is an innovation of chordates that is also used by vertebrates.

摘要

合子基因组激活在包括苍蝇、青蛙和哺乳动物在内的多种系统中得到了广泛研究。然而,对于胚胎发生的最早阶段中基因诱导的确切时间,人们知之甚少。在这里,我们使用高分辨率原位检测方法以及遗传和实验操作,以具有分钟级时间精度的简单模式脊索动物为模型来研究合子激活的时间。我们发现,在 中有两个 同源物是对 FGF 信号做出响应的最早基因。我们提出了一个 FGF 定时机制的证据,该机制由 ERK 介导的 ERF 抑制剂去抑制所驱动。ERF 的耗竭导致 FGF 靶基因在整个胚胎中异位激活。这个定时器的一个亮点是在胚胎发育的 8 细胞期和 16 细胞期之间 FGF 反应性的急剧转变。我们提出,这个定时器是脊索动物的创新,也被脊椎动物所使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63a4/10069452/3c23e65a9a1a/80f01.jpg

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