Gene expression analysis of TFII-I modulated genes in mouse embryonic fibroblasts

被引:5
|
作者
Chimge, Nyam-Osor
Mungunsukh, Ognoon
Ruddle, Frank
Bayarsaihan, Dashzeveg
机构
[1] Univ Louisville, Birth Defects Ctr, Dept Mol Cellular & Craniofacial Biol, Louisville, KY 40202 USA
[2] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
关键词
D O I
10.1002/jez.b.21134
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
TFII-I is a founding member of a family of helix-loop-helix transcription factors involved in modulation of genes through interaction with various nuclear factors and chromatin remodeling complexes. Recent studies indicate that TFII-I performs important function in cell physiology and mouse embryogenesis. In order to understand its molecular role, TFII-I was overexpressed in primary mouse embryonic fibroblasts (MEFs) and alterations in gene expression were monitored with a mouse 16 K oligonucleotide microarray. These studies allowed us to identify genes that lie downstream of TFII-I-dependent pathways. Among the modulated candidates were genes involved in the immunity response, catalytic activity, signaling pathways and transcriptional regulation. Expression of several candidates including those for the interferon-stimulated protein (G1p2), small inducible cytokine A7 (Ccl7), ubiquitin-conjugating enzyme 8 (Ube2l6), cysteine-rich protein (Csrp2) and Drosophila delta-like 1 homolog (Dlk1) were confirmed by real-time PCR. The obtained results suggest that TFII-I participates in multiple signaling and regulatory pathways in MEFs.
引用
收藏
页码:225 / 235
页数:11
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