Monaghan A P, Kaestner K H, Grau E, Schütz G
Division Molecular Biology of the Cell I, German Cancer Research Center, Heidelberg.
Development. 1993 Nov;119(3):567-78. doi: 10.1242/dev.119.3.567.
The HNF-3 alpha, beta and gamma genes constitute a family of transcription factors that are required for hepatocyte-specific gene expression of a number of genes, e.g. transthyretin, alpha-1 antitrypsin and tyrosine aminotransferase. These genes share a highly conserved DNA-binding domain first found in the Drosophila gene, forkhead, which is required for the normal patterning of the developing gut and central nervous system in Drosophila. In adult mouse tissues, transcripts from HNF-3 alpha and beta have been localised to the liver, intestine and lung, whereas HNF-3 gamma is found in the liver, intestine and testis. In light of the early developmental significance of forkhead in Drosophila, we have compared the patterns of expression of HNF-3 alpha, beta and gamma mRNAs during murine embryogenesis. We find that these genes are sequentially activated during development in the definitive endoderm. HNF-3 beta mRNA is expressed in the node at the anterior end of the primitive streak in all three germ layers and is the first gene of this family to be activated. Subsequently, HNF-3 alpha is transcribed in the primitive endoderm in the region of the invaginating foregut and HNF-3 gamma appears upon hindgut differentiation. These genes have different anterior boundaries of mRNA expression in the developing endoderm and transcripts are found in all endoderm-derived structures that differentiate posterior to this boundary. Therefore, we propose that these genes define regionalization within the definitive endoderm. Furthermore, differential mRNA expression of HNF-3 alpha and beta is detected in cells of the ventral neural epithelium, chordamesoderm and notochord. In the neural epithelium, expression of HNF-3 alpha and beta mRNA becomes localised to cells of the floor plate. We propose that, in addition to their characterised requirement for liver-specific gene expression, HNF-3 alpha and beta are required for mesoderm and neural axis formation. We also conclude that HNF-3 beta is the true orthologue of the Drosophila forkhead gene.
肝细胞核因子3α、β和γ基因构成了一个转录因子家族,许多基因(如甲状腺素运载蛋白、α-1抗胰蛋白酶和酪氨酸转氨酶)的肝细胞特异性基因表达都需要这些转录因子。这些基因共享一个高度保守的DNA结合结构域,该结构域最初在果蝇基因叉头蛋白中发现,果蝇发育中的肠道和中枢神经系统的正常模式形成需要该结构域。在成年小鼠组织中,肝细胞核因子3α和β的转录本已定位到肝脏、肠道和肺,而肝细胞核因子3γ则存在于肝脏、肠道和睾丸中。鉴于叉头蛋白在果蝇早期发育中的重要意义,我们比较了小鼠胚胎发育过程中肝细胞核因子3α、β和γ mRNA的表达模式。我们发现这些基因在定形内胚层发育过程中被依次激活。肝细胞核因子3β mRNA在所有三个胚层的原条前端的节点中表达,是该家族中第一个被激活的基因。随后,肝细胞核因子3α在前肠内陷区域的原始内胚层中被转录,肝细胞核因子3γ在中肠分化时出现。这些基因在发育中的内胚层中有不同的mRNA表达前边界,并且在该边界后方分化的所有内胚层衍生结构中都能发现转录本。因此,我们认为这些基因定义了定形内胚层内的区域化。此外,在腹侧神经上皮、脊索中胚层和脊索的细胞中检测到肝细胞核因子3α和β的mRNA差异表达。在神经上皮中,肝细胞核因子3α和β mRNA的表达定位于底板细胞。我们提出,除了它们对肝脏特异性基因表达的已知需求外,肝细胞核因子3α和β对于中胚层和神经轴的形成也是必需的。我们还得出结论,肝细胞核因子3β是果蝇叉头基因的真正直系同源物。