Breier G, Dressler G R, Gruss P
Department of Molecular Cell Biology, Max Planck Institute of Biophysical Chemistry, Göttingen, FRG.
EMBO J. 1988 May;7(5):1329-36. doi: 10.1002/j.1460-2075.1988.tb02948.x.
The murine Hox 3.1 gene maps to a cluster of homeobox-containing genes on chromosome 15. We report the primary structure of the Hox 3.1 protein, as deduced from cDNA sequences, and the expression of Hox 3.1 mRNA during embryogenesis. In addition, a second member of the gene cluster, Hox 3.2, is characterized. The predicted Hox 3.1 protein consists of 242 amino acid residues and has a calculated mol. wt of 28 kd. Besides the homeodomain, it shares with other murine homeodomain proteins a conserved hexapeptide, a region rich in glutamic acid residues at the carboxy terminus and homology at the amino terminus. During embryogenesis, Hox 3.1 transcripts are detected first in the posterior neural tube of 9.5 days post-coital embryos. At later developmental stages, a ventral-dorsal gradient of Hox 3.1 transcript accumulation is established. Hox 3.1 transcripts also are detected in the thoracic sclerotomes from the 6th to the 10th thoracic pre-vertebrae. The data support the hypothesis that the Hox 3.1 gene specifies positional information during murine embryogenesis.
小鼠Hox 3.1基因定位于15号染色体上一组含同源异型框的基因簇。我们报道了从cDNA序列推导得出的Hox 3.1蛋白的一级结构,以及胚胎发育过程中Hox 3.1 mRNA的表达情况。此外,还对该基因簇的第二个成员Hox 3.2进行了特征分析。预测的Hox 3.1蛋白由242个氨基酸残基组成,计算分子量为28kd。除了同源异型域外,它与其他小鼠同源异型域蛋白还共享一个保守的六肽、羧基末端富含谷氨酸残基的区域以及氨基末端的同源性。在胚胎发育过程中,首先在交配后9.5天胚胎的后神经管中检测到Hox 3.1转录本。在随后的发育阶段,建立了Hox 3.1转录本积累的腹背梯度。在第6至第10胸椎前体节的胸节中也检测到了Hox 3.1转录本。这些数据支持了Hox 3.1基因在小鼠胚胎发育过程中指定位置信息的假说。