Regulation of the stem cell leukemia (SCL) gene:: A tale of two fishes

被引:41
作者
Barton, LM
Göttgens, B
Gering, M
Gilbert, JGR
Grafham, D
Rogers, J
Bentley, D
Patient, R
Green, AR [1 ]
机构
[1] Univ Cambridge, Cambridge Inst Med Res, Addenbrookes Hosp, Dept Hematol, Cambridge CB2 2XY, England
[2] Sanger Ctr, Cambridge CB10 1RQ, England
[3] Univ Nottingham, Queens Med Ctr, Inst Genet, Nottingham NG7 2UH, England
基金
英国惠康基金;
关键词
D O I
10.1073/pnas.101532998
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The stem cell leukemia (SQ) gene encodes a tissue-specific basic helix-loop-helix (bHLH) protein with a pivotal role in hemopoiesis and vasculogenesis. Several enhancers have been identified within the murine SCL locus that direct reporter gene expression to subdomains of the normal SCL expression pattern, and long-range sequence comparisons of the human and murine SCL loci have identified additional candidate enhancers. To facilitate the characterization of regulatory elements, we have sequenced and analyzed 33 kb of the SCL genomic locus from the pufferfish Fugu rubripes, a species with a highly compact genome. Although the pattern of SCL expression is highly conserved from mammals to teleost fish, the genes flanking pufferfish SCL were unrelated to those known to flank both avian and mammalian SCL genes. These data suggest that SCL regulatory elements are confined to the region between the upstream and downstream flanking genes, a region of 65 kb in human and 8.5 kb in pufferfish, Consistent with this hypothesis, the entire 33-kb pufferfish Sa locus directed appropriate expression to hemopoietic and neural tissue in transgenic zebrafish embryos, as did a 10.4-kb fragment containing the SQ gene and extending to the 5' and 3' flanking genes. These results demonstrate the power of combining the compact genome of the pufferfish with the advantages that zebrafish provide for studies of gene regulation during development. Furthermore, the pufferfish SCL locus provides a powerful tool for the manipulation of hemopoiesis and vasculogenesis in vivo.
引用
收藏
页码:6747 / 6752
页数:6
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