Stamatoyannopoulos G, Josephson B, Zhang J W, Li Q
Division of Medical Genetics, University of Washington, Seattle 98195.
Mol Cell Biol. 1993 Dec;13(12):7636-44. doi: 10.1128/mcb.13.12.7636-7644.1993.
We report results showing that several gamma gene promoter elements participate in the developmental control of gamma-globin genes. Four gamma gene constructs with 5' truncated at -141, -201, -382, and -730 of the A gamma gene promoter linked to a micro locus control region (microLCR) cassette were used for production of transgenic mice and analysis of gamma gene expression during development. Mice carrying a microLCR -141 A gamma construct displayed downregulation of gamma gene expression in the adult stage of development, indicating that the proximal promoter contains elements participating in gamma gene silencing. Mice carrying a microLCR -201 A gamma or a microLCR -382 A gamma construct displayed high gamma gene expression in the fetal stage of development and complete loss of gamma gene downregulation in the adult stage, suggesting that the -141 to -201 gamma gene sequence contains elements which upregulate gamma gene expression and are dominant over the negative element 3' to -141. Extension of the promoter to -730 resulted in reappearance of gamma gene downregulation, suggesting that the -382 to -730 sequences contain an adult-stage-specific silencer. gamma gene expression in the microLCR -201 A gamma and the microLCR -382 A gamma transgenic mice was copy number dependent. All the microLCR -730 A gamma transgenic mice expressed gamma mRNA; however, gamma gene expression was copy number independent, indicating that levels of gamma gene expression were modulated by the surrounding chromatin. Our results suggest that multiple elements participate in gamma gene silencing. The findings in the microLCR-201 A gamma and microLCR -382 A gamma transgenic mice are interpreted to indicate that the LCR interacts not only with the minimal gamma gene promoter but also with sequences of the upstream promoter. We postulate that gamma gene downregulation is achieved when the interaction between LCR and the upstream promoter is disturbed by the silencer located in the -382 to -730 region. We propose that gamma gene silencing is achieved by the combined effect of negative elements located 3' to -141, the negative element located between -382 and -730, and the competition by the beta gene promoter during the adult stage of development.
我们报告的结果表明,几个γ基因启动子元件参与了γ珠蛋白基因的发育调控。使用四个γ基因构建体,其Aγ基因启动子的5'端在-141、-201、-382和-730处被截断,并与一个微基因座控制区(microLCR)盒相连,用于生产转基因小鼠并分析发育过程中γ基因的表达。携带microLCR -141 Aγ构建体的小鼠在发育的成年阶段显示出γ基因表达的下调,这表明近端启动子包含参与γ基因沉默的元件。携带microLCR -201 Aγ或microLCR -382 Aγ构建体的小鼠在发育的胎儿阶段显示出高γ基因表达,并且在成年阶段完全丧失γ基因下调,这表明-141至-201的γ基因序列包含上调γ基因表达的元件,并且在-141下游的负性元件中占主导地位。将启动子延伸至-730导致γ基因下调再次出现,这表明-382至-730序列包含一个成年期特异性沉默子。microLCR -201 Aγ和microLCR -382 Aγ转基因小鼠中的γ基因表达是拷贝数依赖性的。所有microLCR -730 Aγ转基因小鼠都表达γ mRNA;然而,γ基因表达是拷贝数非依赖性的,这表明γ基因表达水平受周围染色质的调节。我们的结果表明,多个元件参与了γ基因沉默。在microLCR-201 Aγ和microLCR -382 Aγ转基因小鼠中的发现被解释为表明LCR不仅与最小的γ基因启动子相互作用,而且还与上游启动子的序列相互作用。我们推测,当LCR与上游启动子之间的相互作用被位于-382至-730区域的沉默子干扰时,γ基因下调得以实现。我们提出,γ基因沉默是通过位于-141下游的负性元件、位于-382和-730之间的负性元件以及发育成年期β基因启动子的竞争共同作用实现的。