BHLHB4 is a bHLH transcriptional regulator in pancreas and brain that marks the dimesencephalic boundary

被引:33
作者
Bramblett, DE
Copeland, NG
Jenkins, NA
Tsai, MJ
机构
[1] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Program Dev Biol, Houston, TX 77030 USA
[3] NCI, Mouse Canc Genet Program, Frederick, MD 21702 USA
基金
美国国家卫生研究院;
关键词
transcription factor; basic helix-loop-helix protein; phylogeny; diencephalon; pancreatic beta-cells; development; physical chromosome mapping;
D O I
10.1006/geno.2002.6708
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have cloned a basic helix-loop-helix (bHLH) factor gene, Bhlhb4, from a mouse P-cell line. Fluorescence in situ hybridization (FISH) and genetic mapping place Bhlhb4 at the telomeric end of mouse chromosome 2 (H3-H4), syntenic to human chromosome 20q13. Based on phylogenetic analysis, BHLHB4 belongs to a new subgroup of bHLH factors including at least four previously identified mouse bHLH factors: BHLHB5, MIST1, OLIG1, OLIG2, and OLIG3. In the developing nervous system, Bhlhb4 was found to mark the dimesencephalic boundary, suggesting that Bhlhb4 may have a role in diencephalic regionalization. In the pancreas, Bhlhb4 is expressed in a transient fashion that suggests a role in the pancreatic endocrine cell lineage. Transfection experiments show that BHLHB4 can repress transcriptional activation mediated through the pancreatic p-cell specific insulin promoter enhancer RIPE3. Together, these data suggest that BHLHB4 may modulate the expression of genes required for the differentiation and/or maintenance of pancreatic and neuronal cell types.
引用
收藏
页码:402 / 412
页数:11
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