Montoliu L, Umland T, Schütz G
Division of Molecular Biology of the Cell I, German Cancer Research Center, Heidelberg, Germany.
EMBO J. 1996 Nov 15;15(22):6026-34.
We have shown previously that the tyrosinase gene encompassed in a 250 kb yeast artificial chromosome (YAC) is expressed faithfully in transgenic mice. To define the sequences important for this qualitatively and quantitatively correct expression pattern, we have generated transgenic mice with YACs carrying several deletions in the mouse tyrosinase locus. In particular, we wanted to address the in vivo relevance of a regulatory element indicated by a cell-specific DNase I hypersensitive site (HS) located -12 kb upstream of the gene. Wild-type level expression was observed only when the YACs transferred contained this HS. Constructs in which the HS was deleted gave rise to much weaker expression and variable patterns of expression. In conclusion, this HS region appears to harbour the essential regulatory element for the correct expression of the tyrosinase gene. Moreover, it behaves as a locus control region in that it commands the functional status of this expression domain, protecting it from position effects.
我们之前已经表明,包含在一个250 kb酵母人工染色体(YAC)中的酪氨酸酶基因在转基因小鼠中能得到忠实表达。为了定性和定量地确定对这种正确表达模式至关重要的序列,我们构建了携带小鼠酪氨酸酶基因座若干缺失的YAC转基因小鼠。特别地,我们想要研究位于该基因上游-12 kb处一个细胞特异性的DNA酶I超敏位点(HS)所指示的调控元件在体内的相关性。只有当转入的YAC包含这个HS时,才能观察到野生型水平的表达。缺失HS的构建体导致表达弱得多且表达模式可变。总之,这个HS区域似乎包含酪氨酸酶基因正确表达所必需的调控元件。此外,它表现为一个基因座控制区,因为它控制这个表达域的功能状态,保护其免受位置效应的影响。