在小鼠体内破坏 Iqsec1 会导致胚胎死亡,内脏内胚层的大顶端空泡减少。

IF 3.5 4区 生物学 Q1 Biochemistry, Genetics and Molecular Biology FEBS Letters Pub Date : 2024-11-19 DOI:10.1002/1873-3468.15058
Hiroyuki Sakagami, Tomoko Shiroshima, Noriko Nemoto, Tomoko Niimura, Takeyuki Sugawara, Yoshinobu Hara, Koji Saito, Tadashi Okubo, Masahiro Fukaya
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引用次数: 0

摘要

Iqsec1(IQ motif and Sec7 domain-containing protein 1)又称BRAG2(Brefeldin A-resistant Arf-GEF 2),是一种鸟嘌呤核苷酸交换因子,它通过激活II类和III类ADP-核糖基化因子来调节膜贩运、细胞骨架组织和信号转导。为了研究Iqsec1在整个动物水平上的生理作用,我们利用CRISPR/Cas9介导的基因编辑技术产生了Iqsec1缺陷小鼠。几乎所有 Iqsec1-/- 小鼠(99%)都表现出胚胎致死和严重的生长迟缓。电子显微镜显示,与对照组相比,Iqsec1-/-胚胎在胚胎第8.5天时,卵黄囊内脏内胚层细胞缺乏大的顶端空泡。这些研究结果表明,Iqsec1 在胚胎发生过程中发挥着关键作用,很可能是通过调节内脏内胚层细胞的膜运输。
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Disruption of Iqsec1 in mice leads to embryonic lethality with reduced large apical vacuoles in the visceral endoderm.

Iqsec1 (IQ motif and Sec7 domain-containing protein 1), also known as BRAG2 (Brefeldin A-resistant Arf-GEF 2), is a guanine nucleotide exchange factor that regulates membrane trafficking, cytoskeletal organization, and signal transduction by activating class II and III ADP-ribosylation factors. To investigate the physiological role of Iqsec1 at the whole animal level, we generated Iqsec1-deficient mice using CRISPR/Cas9-mediated gene editing. Nearly all Iqsec1-/- mice (99%) exhibited embryonic lethality with severe growth retardation. Electron microscopy revealed that Iqsec1-/- embryos at embryonic day 8.5 lacked large apical vacuoles in visceral endoderm cells of the yolk sac, compared with controls. These findings suggest that Iqsec1 plays a critical role in embryogenesis, likely through regulation of membrane trafficking in visceral endoderm cells.

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来源期刊
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
7.00
自引率
2.90%
发文量
303
审稿时长
1.0 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
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