The mts1/S100A4 gene encodes a small acidic calcium-binding protein that is expressed in a cell-specific manner in development, tumorigenesis and certain tissues of adult mice. A composite enhancer that is active in murine mammary adenocarcinoma cells was previously identified in the first intron of the mts1/S100A4 gene. Here we present a detailed analysis of the structure and function of this enhancer in the Mts1/S100A4-expressing CSML100 and non-expressing CSML0 mouse adenocarcinoma cell lines. In CSML100 cells the enhancer activity is composed of at least six cis-elements interacting with Sp1 and AP-1 family members and CBF/AML/PEBP2 and KRC transcription factors. In addition, a minisatellite-like DNA sequence significantly contributes to the enhancer activity via interaction with abundant proteins, which likely have been described previously under the name minisatellite-binding proteins. Extensive mutational analysis of the mts1/S100A4 enhancer revealed a cooperative function of KRC and the factors binding minisatellite DNA. This is the first example of an enhancer where two nuclear factors earlier implicated in different recombination processes cooperate to activate transcription. In Mts1/S100A4-negative CSML0 cells the strength of the enhancer was 7- to 12.5-fold lower compared to that in CSML100 cells, when referred to the activities of three viral promoters. In CSML0 cells the enhancer could be activated by exogenous AP-1 and CBF transcription factors.

译文

:mts1 / S100A4基因编码一种小的酸性钙结合蛋白,该蛋白在成年小鼠的发育,肿瘤发生和某些组织中以细胞特异性方式表达。先前在mts1 / S100A4基因的第一个内含子中鉴定出了一种在鼠乳腺腺癌细胞中有活性的复合增强子。在这里,我们目前在表达Mts1 / S100A4的CSML100和非表达CSML0小鼠腺癌细胞系中对该增强子的结构和功能进行详细分析。在CSML100细胞中,增强子活性由至少六个与Sp1和AP-1家族成员以及CBF / AML / PEBP2和KRC转录因子相互作用的顺式元件组成。另外,类似小卫星的DNA序列通过与丰富的蛋白质相互作用而显着地促进了增强子的活性,这可能先前已经以小卫星结合蛋白的名称进行了描述。对mts1 / S100A4增强子的广泛突变分析揭示了KRC和结合小卫星DNA的因子的协同功能。这是增强子的第一个例子,其中先前涉及不同重组过程的两个核因子协同激活转录。在Mts1 / S100A4阴性CSML0细胞中,与三种病毒启动子的活性相比,增强子的强度比CSML100细胞低7到12.5倍。在CSML0细胞中,增强子可以被外源AP-1和CBF转录因子激活。

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