CAJ | 학술논문

目的：研究小鼠舌肌发育的分子调控机制。方法：取胚胎第13．25天（E13．25）及 E15．5小鼠舌组织。应用 Affy-metrix Mouse GeneChip，对胎鼠舌发育过程中的差异基因进行筛选。应用 DAVID 网络分析工具对基因进行功能和聚类分析。结果：基因功能和聚类分析表明，在 E13．25高表达的基因主要与细胞周期相关因子（Exo1、Gsk3B、Kif20b、Skp2）和细胞粘附因子（Neo1、lama1）等相关。在 E15．5高表达的基因主要与细胞骨架（titin、Hspb7）相关。结论：小鼠舌组织增殖和特化与细胞周期和细胞粘附基因相关，舌组织分化和成熟主要与细胞骨架相关。
목적：연구소서설기발육적분자조공궤제。방법：취배태제13．25천（E13．25）급 E15．5소서설조직。응용 Affy-metrix Mouse GeneChip，대태서설발육과정중적차이기인진행사선。응용 DAVID 망락분석공구대기인진행공능화취류분석。결과：기인공능화취류분석표명，재 E13．25고표체적기인주요여세포주기상관인자（Exo1、Gsk3B、Kif20b、Skp2）화세포점부인자（Neo1、lama1）등상관。재 E15．5고표체적기인주요여세포골가（titin、Hspb7）상관。결론：소서설조직증식화특화여세포주기화세포점부기인상관，설조직분화화성숙주요여세포골가상관。
Objective:To gain insight into the molecular mechanisms associated with mouse tongue myogenesis.Methods:Different genes in the tongue at mouse embryonic day 13.25 (E13.25)and 15.5 was investigated using Affymetrix Mouse GeneChip.Using the twice significance of difference as the standard,the molecular mechanisms of tongue development were studied and several molecules re-lated were identified by DAVID functional annotation clustering analysis.Results:Genes of higher expression level at E13.25 were re-lated to cell cycle and cell adhesion,of whom Exo1 ,Gsk3B,Kif20b,Skp2 (cell cycle related factors)and Neo1 and lama1 (cell adhe-sion factors)were activated.While genes of higher expression level at E15.5 were related to cytoskeleton,such as titin and Hspb7. Conclusions:The proliferation and determination of tongue were related with gene clusters of cell cycle and cell adhesion,and,differen-tiation and maturation of tongue were relevant to gene cluster of cytoskeleton.It had highlighted potential cascades and important candi-dates for further investigation on the genetic mechanism and clinical therapy of tongue related diseases.