Identification of target genes regulated by PAX3 and PAX3-FKHR in embryogenesis and alveolar rhabdomyosarcoma

被引:55
作者
Barber, TD
Barber, MC
Tomescu, O
Barr, FG
Ruben, S
Friedman, TB
机构
[1] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Human Genome Sci Inc, Dept Preclin Discovery, Rockville, MD 20850 USA
[3] Michigan State Univ, Grad Program Genet, E Lansing, MI 48824 USA
[4] Natl Inst Deafness & Other Commun Disorders, NIH, Rockville, MD 20850 USA
关键词
CASTing; PAX3; Waardenburg; cancer; ARMS; FKHR; EN2; TGFA; VEGF; Itm2A; and BVES;
D O I
10.1006/geno.2002.6703
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
PAX3 is a transcription factor important for neural, muscle, and facial development in vertebrates. To identify genes regulated by PAX3, we used a cyclic amplification and selection of targets (CASTing) strategy to isolate cis-regulatory elements bound by PAX3. CASTing libraries were constructed with mouse DNA fragments bound by mouse PAX3, and human genomic DNA fragments bound by human PAX3 and the fusion protein PAX3-FKHR. Approximately 1000 clones were sequenced from each of these three libraries. Numerous putative targets of PAX3 and PAX3-FKHR were identified and six genes, Itm2A, Fath, FLT1, TGFA, BVES, and EN2, were examined closely. The genomic DNA fragments near these genes contain PAX3 binding sites and confer PAX3-dependent regulation. The expression levels of these genes correlate with the PAX3 expression levels in mouse embryos or with PAX3-FKHR expression levels in rhabdomyosarcoma cell lines, and indicate they may be part of the PAX3 regulatory circuitry during embryogenesis and tumor formation.
引用
收藏
页码:278 / 284
页数:7
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