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Myc与USF:cad基因处的区分由核心启动子元件决定。

Myc versus USF: discrimination at the cad gene is determined by core promoter elements.

作者信息

Boyd K E, Farnham P J

机构信息

McArdle Laboratory for Cancer Research, University of Wisconsin Medical School, Madison 53706, USA.

出版信息

Mol Cell Biol. 1997 May;17(5):2529-37. doi: 10.1128/MCB.17.5.2529.

Abstract

Carbamoyl-phosphate synthase/aspartate carbamoyltransferase/dihydroorotase, which is encoded by the cad gene, is required for the first three rate-limiting steps of de novo pyrimidine biosynthesis. It has been previously demonstrated that cad transcription increases at the G1/S-phase boundary, as quiescent cells reenter the proliferative cell cycle. The growth-responsive element has been mapped to an E box at +65 in the hamster cad promoter. Using an in vivo UV cross-linking and immunoprecipitation assay, we show that Myc, Max, and upstream stimulatory factor (USF) bind to the chromosomal cad promoter. To determine whether binding of Myc-Max or USF is critical for cad growth regulation, we analyzed promoter constructs which contain mutations in the nucleotides flanking the E box. We demonstrate that altering nucleotides which flank the cad E box to sequences which decrease Myc-Max binding in vitro correlates with a loss of cad G1/S-phase transcriptional activation. This result supports the conclusion that binding of Myc-Max, but not USF, is essential for cad regulation. Our investigations demonstrate that the endogenous cad E box can be bound by more than one transcription factor, but growth-induced cad expression is achieved only by Myc.

摘要

由cad基因编码的氨甲酰磷酸合成酶/天冬氨酸氨甲酰转移酶/二氢乳清酸酶,是嘧啶从头合成前三个限速步骤所必需的。先前已经证明,随着静止细胞重新进入增殖细胞周期,cad转录在G1/S期边界增加。生长反应元件已定位到仓鼠cad启动子中+65处的一个E盒。使用体内紫外线交联和免疫沉淀试验,我们表明Myc、Max和上游刺激因子(USF)与染色体cad启动子结合。为了确定Myc-Max或USF的结合对于cad生长调节是否至关重要,我们分析了在E盒侧翼核苷酸中含有突变的启动子构建体。我们证明,将cad E盒侧翼的核苷酸改变为在体外降低Myc-Max结合的序列,与cad G1/S期转录激活的丧失相关。这一结果支持了Myc-Max而非USF的结合对于cad调节至关重要的结论。我们的研究表明,内源性cad E盒可被不止一种转录因子结合,但生长诱导的cad表达仅通过Myc实现。

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