Hedlund Eva, Karsten Stanislav L, Kudo Lili, Geschwind Daniel H, Carpenter Ellen M
Department of Psychiatry, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
J Neurosci Res. 2004 Feb 1;75(3):307-19. doi: 10.1002/jnr.10844.
Hoxd10 is expressed in the posterior spinal cord and hindlimbs of the mouse. Hoxd10, along with other Hox transcription factors, is thought to regulate the activity of genes involved in nervous system patterning and motor neuron development, but little is known about the downstream targets regulated by this gene. cDNA microarrays were used to investigate the transcriptional network regulated by Hoxd10 in homozygous knockout animals. Sixty-nine genes were identified with altered expression levels in mutant spinal cords. Among these were genes involved in such diverse cellular events as cellular communication, cell cycle control, development and differentiation, and neuronal survival. The expression of some of these genes was investigated using reverse transcriptase-polymerase chain reaction (RT-PCR) and in situ hybridization. Nine genes showed changes in expression of the same sign and similar magnitude using RT-PCR in Hoxd10 single mutant animals, with additional changes in expression seen in Hoxa10/Hoxd10 double mutant animals. In situ hybridization studies also demonstrated changes in expression consistent with microarray results. Analysis of putative promoter regions for Hox protein binding sites suggested that some genes may be direct Hoxd10 targets, whereas others likely are regulated through intermediate steps. Using cDNA microarrays to study a single gene knockout during critical developmental stages has identified a large number of genes regulated by Hoxd10, many of which would not have been approached as candidates for Hox gene regulation based on function or expression.
Hoxd10在小鼠的脊髓后部和后肢中表达。Hoxd10与其他Hox转录因子一起,被认为可调节参与神经系统模式形成和运动神经元发育的基因的活性,但对于受该基因调控的下游靶点却知之甚少。利用cDNA微阵列研究纯合敲除动物中受Hoxd10调控的转录网络。在突变的脊髓中鉴定出69个表达水平发生改变的基因。其中包括参与细胞通讯、细胞周期控制、发育与分化以及神经元存活等多种细胞事件的基因。使用逆转录聚合酶链反应(RT-PCR)和原位杂交对其中一些基因的表达进行了研究。在Hoxd10单突变动物中,9个基因通过RT-PCR显示出相同方向且幅度相似的表达变化,在Hoxa10/Hoxd10双突变动物中还观察到了额外的表达变化。原位杂交研究也证实了与微阵列结果一致的表达变化。对Hox蛋白结合位点的假定启动子区域进行分析表明,一些基因可能是Hoxd10的直接靶点,而其他基因可能是通过中间步骤进行调控的。利用cDNA微阵列在关键发育阶段研究单个基因敲除,已鉴定出大量受Hoxd10调控的基因,其中许多基于功能或表达情况本不会被视为Hox基因调控的候选基因。