So Ju-Hoon, Kim Jun-Dae, Yoo Kyeong-Won, Kim Hyun-Taek, Jung Seung-Hyun, Choi Jung-Hwa, Lee Mi-Sun, Jin Suk-Won, Kim Cheol-Hee
Department of Biology, Chungnam National University, Daejeon, Korea; Department of Developmental Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Yale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut, United States of America.
PLoS One. 2014 Oct 27;9(10):e109517. doi: 10.1371/journal.pone.0109517. eCollection 2014.
It has been shown that Mindbomb (Mib), an E3 Ubiquitin ligase, is an essential modulator of Notch signaling during development. However, its effects on vascular development remain largely unknown.
We identified a number of novel proteins that physically interact with Mib, including the Factor Inhibiting Hypoxia Inducible Factor 1 (FIH-1, also known as HIF1AN) from a yeast two hybrid screen, as previously reported. In cultured cells, FIH-1 colocalizes with Mib1, corroborating their potential interaction. In zebrafish embryos, FIH-1 appears to modulate VEGF-A signaling activity; depletion of fih-1 induces ectopic expression of vascular endothelial growth factor-a (vegfa) and leads to exuberant ectopic sprouts from intersegmental vessels (ISVs). Conversely, over-expression of fih-1 substantially attenuates the formation of ISVs, which can be rescued by concurrent over-expression of vegfa, indicating that FIH-1/HIF1AN may fine tune VEGF-A signaling.
Taken together, our data suggest that FIH-1 interacts with Mib E3 Ubiquitin ligase and modulates vascular development by attenuating VEGF-A signaling activity.
已有研究表明,E3泛素连接酶Mindbomb(Mib)是发育过程中Notch信号通路的关键调节因子。然而,其对血管发育的影响仍不清楚。
如先前报道,我们通过酵母双杂交筛选鉴定出许多与Mib发生物理相互作用的新蛋白,包括抑制缺氧诱导因子1(FIH-1,也称为HIF1AN)。在培养细胞中,FIH-1与Mib1共定位,证实了它们之间的潜在相互作用。在斑马鱼胚胎中,FIH-1似乎可调节VEGF-A信号活性;敲除fih-1可诱导血管内皮生长因子-a(vegfa)异位表达,并导致节间血管(ISV)产生大量异位芽。相反,过表达fih-1可显著减弱ISV的形成,同时过表达vegfa可使其恢复,这表明FIH-1/HIF1AN可能对VEGF-A信号进行微调。
综上所述,我们的数据表明FIH-1与Mib E3泛素连接酶相互作用,并通过减弱VEGF-A信号活性来调节血管发育。