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连接蛋白43基因敲除星形胶质细胞中基因表达的阵列分析。

Array analysis of gene expression in connexin-43 null astrocytes.

作者信息

Iacobas Dumitru A, Urban-Maldonado Marcia, Iacobas Sanda, Scemes Eliana, Spray David C

机构信息

Department of Neuroscience, Albert Einstein College of Medicine, New York 10461, USA.

出版信息

Physiol Genomics. 2003 Nov 11;15(3):177-90. doi: 10.1152/physiolgenomics.00062.2003.

Abstract

Connexin-43 (Cx43) is the most abundant gap junction protein in brain, where it is found primarily between astrocytes. Although the morphology of astrocytes from Cx43-null (knockout, KO) mice is similar to that of wild-type (WT) astrocytes, KO astrocytes exhibit reduced growth rate in culture. To evaluate the impact of deletion of Cx43 on other genes, including those encoding cell cycle proteins, we used DNA arrays to determine expression patterns in cultured astrocytes from sibling Cx43-null and WT mice. RNA samples extracted from astrocytes cultured from WT and Cx43-null neonatal mice were dye labeled and individually cohybridized with a reference of labeled cDNAs pooled from a variety of tissues on 8 gene arrays containing 8,975 mouse DNA sequences. Normal variability in expression of each gene was evaluated and incorporated into "expression scores" to statistically compare expression levels between WT and KO samples. In Cx43-null astrocytes, 4.1% of the 4,998 adequately quantifiable spots were found to have significantly (P < 0.05) decreased hybridization compared with controls, and 9.4% of the spots showed significantly higher hybridization. The significantly different spots corresponded to RNAs encoding 252 known proteins, many not previously linked to gap junctions, including transcription factors, channels and transporters, cell growth and death signals, enzymes and cell adhesion molecules. These data indicate a surprisingly high degree of impact of deletion of Cx43 on other astrocyte genes, implying that gap junction gene expression alters numerous processes in addition to intercellular communication.

摘要

连接蛋白43(Cx43)是大脑中含量最丰富的间隙连接蛋白,主要存在于星形胶质细胞之间。尽管来自Cx43基因敲除(KO)小鼠的星形胶质细胞形态与野生型(WT)星形胶质细胞相似,但KO星形胶质细胞在培养中的生长速率降低。为了评估Cx43缺失对其他基因(包括编码细胞周期蛋白的基因)的影响,我们使用DNA阵列来确定来自同胞Cx43基因敲除和WT小鼠的培养星形胶质细胞中的表达模式。从WT和Cx43基因敲除新生小鼠培养的星形胶质细胞中提取的RNA样本进行染料标记,并分别与从多种组织中汇集的标记cDNA参考物在包含8975个小鼠DNA序列的8个基因阵列上进行共杂交。评估每个基因表达的正常变异性,并将其纳入“表达分数”,以统计学比较WT和KO样本之间的表达水平。在Cx43基因敲除的星形胶质细胞中,发现4998个可充分定量的斑点中有4.1%与对照相比杂交显著降低(P < 0.05),9.4%的斑点显示杂交显著升高。差异显著的斑点对应于编码252种已知蛋白质的RNA,其中许多以前未与间隙连接相关联,包括转录因子、通道和转运蛋白、细胞生长和死亡信号、酶和细胞粘附分子。这些数据表明Cx43缺失对其他星形胶质细胞基因的影响程度惊人地高,这意味着间隙连接基因表达除了影响细胞间通讯外,还会改变许多其他过程。

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