Crish James F, Bone Frederic, Banks Eric B, Eckert Richard L
Department of Physiology and Biophysics, Case Western Reserve University School of Medicine, 2109 Adelbert Road, Cleveland, Ohio, OH 44106-4970, USA.
Oncogene. 2002 Jan 24;21(5):738-47. doi: 10.1038/sj.onc.1205038.
Human involucrin (hINV) is a keratinocyte protein that is expressed in the suprabasal compartment of the epidermis and other stratifying surface epithelia. Involucrin gene expression is initiated early in the differentiation process and is maintained until terminal cell death. The distal regulatory region (DRR) is a segment of the hINV promoter (nucleotides -2473/-1953) that accurately recapitulates the normal pattern of suprabasal (spinous and granular layer) expression in transgenic mouse epithelia. To identify sequences that mediate expression at specific stages of differentiation, we divided the DRR into two segments, a 376 nucleotide upstream region (DRR(-2473/-2100)) and a 147 nucleotide downstream region (DRR(-2100/-1953)), and evaluated the ability of these sequences to drive expression in transgenic mice. The DRR(-2473/-2100) segment drives expression at a level comparable to that observed for the DRR, but expression is restricted to the upper granular layers (i.e., no spinous layer expression). In contrast, the DRR(-2100/-1953) segment does not drive expression. However, reassembling the DRR restores the complete range of expression. These results suggest that two distinct, spatially-separate elements are required to specify the complete differentiation-dependent program of involucrin gene expression. To identify specific transcription factor binding sites involved in this regulation, we mutated an activator protein-1 binding site, AP1-5, located within DRR(-2473/-2100) segment. This site binds AP1 transcription factors present in mouse epidermal extracts, and its mutation eliminates appropriate hINV expression. This result suggests that AP1 factors participate as components of a multi-component transcription factor complex that is required for regulation.
人内披蛋白(hINV)是一种角质形成细胞蛋白,在表皮的基底上层以及其他分层的表面上皮中表达。内披蛋白基因表达在分化过程早期启动,并持续至细胞终末死亡。远端调控区(DRR)是hINV启动子的一个片段(核苷酸-2473/-1953),可精确重现转基因小鼠上皮中基底上层(棘层和颗粒层)的正常表达模式。为了鉴定在分化特定阶段介导表达的序列,我们将DRR分为两个片段,一个376个核苷酸的上游区域(DRR(-2473/-2100))和一个147个核苷酸的下游区域(DRR(-2100/-1953)),并评估这些序列在转基因小鼠中驱动表达的能力。DRR(-2473/-2100)片段驱动的表达水平与DRR观察到的水平相当,但表达仅限于上部颗粒层(即无棘层表达)。相比之下,DRR(-2100/-1953)片段不驱动表达。然而,重新组装DRR可恢复完整的表达范围。这些结果表明,需要两个不同的、空间上分离的元件来指定内披蛋白基因表达的完整分化依赖性程序。为了鉴定参与这种调控的特定转录因子结合位点,我们对位于DRR(-2473/-2100)片段内的一个激活蛋白-1结合位点AP1-5进行了突变。该位点结合小鼠表皮提取物中存在的AP1转录因子,其突变消除了适当的hINV表达。这一结果表明,AP1因子作为调控所需的多组分转录因子复合物的组成部分发挥作用。