Groupe de Biologie Expérimentale, Laboratoire de Biologie du Développement, CNRS UMR 7622, Université Pierre et Marie Curie, 9 quai Saint-Bernard, 75005 Paris, France.
Mech Dev. 2010 May-Jun;127(5-6):281-91. doi: 10.1016/j.mod.2010.03.002. Epub 2010 Mar 23.
RNA-binding proteins play an important role to post-transcriptionally regulate gene expression. During early development they exhibit temporally and spatially regulated expression pattern. The expression of Xenopus laevis Seb4 gene, also known as RBM24 in other vertebrates, is restricted to the lateral and ventral mesoderm during gastrulation and then localized to the somitic mesoderm, in a similar pattern as XMyoD gene. Using a hormone-inducible form of MyoD to identify potential direct MyoD target genes, we find that Seb4 expression is directly regulated by MyoD at the gastrula stage. We further show that a 0.65kb X. tropicalis RBM24 regulatory region contains multiple E boxes (CANNTG), which are potential binding sites for MyoD and other bHLH proteins. By injecting a RBM24 reporter construct into the animal pole of X. laevis embryos, we find that this reporter gene is indeed specifically activated by MyoD and repressed by a dominant negative MyoD mutant. Knockdown of Seb4 produces similar effects as those obtained by the dominant negative MyoD mutant, indicating that it is required for the expression of myogenic genes and myogenesis in the embryo. In cultured ectodermal explants, although overexpression of Seb4 has no obvious effect on myogenesis, knockdown of Seb4 inhibits the expression of myogenic genes and myogenesis induced by MyoD. These results reveal that Seb4 is a target of MyoD during myogenesis and is required for myogenic gene expression.
RNA 结合蛋白在后转录水平上调节基因表达中起着重要作用。在早期发育过程中,它们表现出时间和空间上的调节表达模式。非洲爪蟾 Seb4 基因(在其他脊椎动物中也称为 RBM24)的表达在原肠胚期仅限于侧部和腹侧中胚层,然后定位于体节中胚层,与 XMyoD 基因的表达模式相似。使用激素诱导型 MyoD 来鉴定潜在的直接 MyoD 靶基因,我们发现 Seb4 表达在原肠胚期受到 MyoD 的直接调节。我们进一步表明,0.65kb 的 X. tropicalis RBM24 调控区含有多个 E 盒(CANNTG),这些 E 盒是 MyoD 和其他 bHLH 蛋白的潜在结合位点。通过将 RBM24 报告基因构建体注射到非洲爪蟾胚胎的动物极,我们发现该报告基因确实可以被 MyoD 特异性激活,并且被显性负性 MyoD 突变体抑制。Seb4 的敲低产生的效果与显性负性 MyoD 突变体获得的效果相似,表明它对于胚胎中肌源性基因的表达和肌发生是必需的。在培养的外胚层外植体中,尽管 Seb4 的过表达对肌发生没有明显影响,但 Seb4 的敲低抑制了 MyoD 诱导的肌源性基因的表达和肌发生。这些结果表明 Seb4 是肌发生过程中 MyoD 的靶标,并且对于肌源性基因的表达是必需的。