首页> 外文期刊>Brain research >Laser capture microdissection and cDNA array analysis for identification of mouse KIAA/FLJ genes differentially expressed in the embryonic dorsal spinal cord.
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Laser capture microdissection and cDNA array analysis for identification of mouse KIAA/FLJ genes differentially expressed in the embryonic dorsal spinal cord.

机译:激光捕获显微切割和cDNA阵列分析,用于鉴定在胚胎背脊髓中差异表达的小鼠KIAA / FLJ基因。

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摘要

During early development, centrally projecting dorsal root ganglion (DRG) neurons extend their axons toward the dorsal spinal cord. We previously reported that this projection is achieved by dorsal spinal cord-derived chemoattraction. However, the molecular nature of the chemotrophic cue is not yet fully understood. To identify novel genes differentially expressed in the dorsal spinal cord in the embryonic day 10.5 mouse, we used the Kazusa cDNA array system comprising approximately 1700 mouse KIAA/FLJ (mKIAA/mFLJ) cDNA clones and laser capture microdissection (LCM) in combination with PCR-based cDNA amplification. We observed that a certain population of genes showed significantly increased expression in the dorsal spinal cord. In situ hybridization analysis verified the expression of mRNAs of 6 genes (Hip1r, Nav2, Fstl5, Cacna1h, Bcr, and Bmper) in the cells that constitute the dorsal spinal cord. The dorsal spinal cord-specific genes identified in this study provide a basis for studying the molecular nature of the neural development including the axonal guidance of DRG neurons. These results also demonstrate that the combined use of LCM coupled with the Kazusa cDNA array technology will be useful for the identification of large proteins expressed in the restricted small regions of embryos.
机译:在早期发育过程中,中央突出的背根神经节(DRG)神经元将其轴突伸向背脊髓。我们先前曾报道过这种投影是通过背脊髓衍生的化学引力实现的。但是,对化学营养指示的分子性质尚未完全了解。为了鉴定在胚胎第10.5天小鼠的背脊髓中差异表达的新基因,我们使用了Kazusa cDNA阵列系统,该系统包含约1700个小鼠KIAA / FLJ(mKIAA / mFLJ)cDNA克隆和激光捕获显微切割(LCM),并与PCR结合使用基于cDNA的扩增。我们观察到一定数量的基因在背脊髓中显示出明显增加的表达。原位杂交分析验证了构成背脊髓的细胞中6个基因(Hip1r,Nav2,Fstl5,Cacna1h,Bcr和Bmper)的mRNA表达。这项研究中确定的背脊髓特异基因为研究神经发育的分子性质(包括DRG神经元的轴突引导)提供了基础。这些结果还表明,结合使用LCM和Kazusa cDNA阵列技术,可用于鉴定在胚胎的受限小区域表达的大蛋白。

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