Gong Baiwei, Liang Dong, Chew Ting-Gang, Ge Ruowen
Faculty of Science, Department of Biological Sciences, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260, Singapore.
Biochim Biophys Acta. 2004 Jan 5;1676(1):33-40. doi: 10.1016/j.bbaexp.2003.10.006.
Vascular endothelial growth factor (VEGF-A) is a key angiogenic growth factor which regulates vertebrate embryonic vascularization, adult physiology such as wound healing and reproduction as well as many human diseases. To understand the evolution and regulation of this gene in vertebrates, we have isolated and characterized the zebrafish vegf-A gene and compared it with VEGF-A genes of human, mouse as well as an in silico isolated VEGF-A homologue from pufferfish. Our results indicate that the zebrafish vegf-A gene is organized similarly to mammalian and Fugu VEGF-A genes, with eight exons interrupted by seven introns. However, zebrafish vegf-A introns are generally larger than mammalian introns while Fugu VEGF-A introns are much smaller. Furthermore, zebrafish exon 6 (z6) has a unique sequence while Fugu's exon 6 is highly homologous to the mammalian counterparts. Alternative splicing generates multiple vegf-A mRNA isoforms in zebrafish with Vegf(121) as the dominant isoform in adult and Vegf(165) as the dominant isoform in early embryos. The exon z6 containing isoform Vegf(12345z678) is only detected in heart, muscle, and early embryos while another isoform Vegf-A(1234577)(a)(8) is only detected in heart. Furthermore, no conserved 5' flanking sequences between zebrafish and Fugu were observed while numerous conserved regions exist between human and mouse in this area. These results suggest both conserved and diverged functions of VEGF-A from fish to mammals since the separation of these two groups from their common ancestor about 450 million years ago and a diverged regulation of this gene since the separation of zebrafish from Fugu. These data will be valuable for future studies of VEGF-A gene regulation and function in different vertebrates.
血管内皮生长因子(VEGF - A)是一种关键的血管生成生长因子,它调节脊椎动物胚胎血管形成、成人生理学过程(如伤口愈合和生殖)以及许多人类疾病。为了了解该基因在脊椎动物中的进化和调控,我们分离并鉴定了斑马鱼vegf - A基因,并将其与人类、小鼠的VEGF - A基因以及通过计算机分离的河豚VEGF - A同源物进行比较。我们的结果表明,斑马鱼vegf - A基因的组织方式与哺乳动物和河豚的VEGF - A基因相似,有八个外显子被七个内含子打断。然而,斑马鱼vegf - A内含子通常比哺乳动物内含子大,而河豚VEGF - A内含子则小得多。此外,斑马鱼外显子6(z6)具有独特序列,而河豚的外显子6与哺乳动物对应物高度同源。可变剪接在斑马鱼中产生多种vegf - A mRNA异构体,Vegf(121)是成体中的主要异构体,Vegf(165)是早期胚胎中的主要异构体。包含外显子z6的异构体Vegf(12345z678)仅在心脏、肌肉和早期胚胎中检测到,而另一种异构体Vegf - A(1234577)(a)(8)仅在心脏中检测到。此外,在斑马鱼和河豚之间未观察到保守的5'侧翼序列,而在人类和小鼠的该区域存在许多保守区域。这些结果表明,自约4.5亿年前这两组从共同祖先分离以来,VEGF - A从鱼类到哺乳动物具有保守和分化的功能,并且自斑马鱼与河豚分离以来该基因存在分化的调控。这些数据对于未来研究不同脊椎动物中VEGF - A基因的调控和功能将具有重要价值。