Laser capture microdissection and cDNA array analysis for identification of mouse KIAA/FLJ genes differentially expressed in the embryonic dorsal spinal cord

被引:17
作者
Masuda, Tomoyuki [1 ]
Kai, Nobuyuki [2 ]
Sakuma, Chie [1 ]
Kobayashi, Kazuto [2 ]
Koga, Hisashi [3 ]
Yaginuma, Hiroyuki [1 ]
机构
[1] Fukushima Med Univ, Sch Med, Dept Anat, Fukushima 9601295, Japan
[2] Fukushima Med Univ, Sch Med, Inst Biomed Sci, Dept Mol Genet, Fukushima 9601295, Japan
[3] Kazusa DNA Res Inst, Dept Human Genome Res, Med Genet Lab, Chiba 2920108, Japan
关键词
Laser capture microdissection; cDNA microarray; Spinal cord; Mouse KIAA gene; Mouse embryo; INITIAL TRAJECTORIES; SENSORY AXONS; CELL-ADHESION; CYTOSKELETON; GUIDANCE; PROTEIN; FAMILY; BRAIN;
D O I
10.1016/j.brainres.2008.10.028
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
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 micro dissection (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, Nau2, 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. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:61 / 67
页数:7
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