[Mapping of FHL2 transcription activation domain].

Jing-Hua Yan, Qi-Nong Ye, Yan Fang, Jian-Hua Zhu, Cui-Fen Huang
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Abstract

FHL2, a member of LIM-only protein family, plays an important role in transcription regulation, apoptosis, cancer development and progression. In this study, a mammalian transcription activation system was constructed by using DNA binding domain(DBD) of GAL4 and luciferase reporter gene with DBD binding sequence, and used for mapping of FHL2 transcription activation domain. First, the coding sequence of GAL4-DBD was inserted into expression vector pcDNA3, generating the pDBD recombinant plasmid, then the wild-type FHL2 and its mutants were fused in-frame with GAL4-DBD, resulting in expression vectors for wild-type FHL2 and its mutants. All of the recombinant plasmids were transfected into 293T cells. Western blot assay showed that all of the fusion proteins were expressed. The analysis of FHL2 transcription activation properties by using the GAL4-luciferase reporter gene indicated that wild-type FHL2 had activation activity in both 293T and MCF-7 cells. The deletion of the half LIM domain at the N-terminus severely impaired the capacity of FHL2 to stimulate transcription. The mutant lacking the LIM domain at the C-terminus was totally inactive, while the deletion of two LIM domains at the C-terminus partially recovered its ability to stimulate transcription. The deletion of the second LIM domain at C-terminus did not alter the activation capacity of FHL2. These results suggest that the last LIM domain at the C-terminus of FHL2 is critical for its transcription activation function, the second LIM domain at the C-terminus may be a negative regulation region, but this negative regulation depends on the last LIM domain. Mapping of transcription activation domain of FHL2 lays solid basis for further study on various FHL2 functions.

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[FHL2转录激活域的定位]。
FHL2是LIM-only蛋白家族成员,在转录调控、细胞凋亡、肿瘤发生进展等方面发挥重要作用。本研究利用GAL4的DNA结合域(DBD)和具有DBD结合序列的荧光素酶报告基因构建了哺乳动物转录激活系统,并用于FHL2转录激活域的定位。首先将GAL4-DBD的编码序列插入到表达载体pcDNA3中,生成pDBD重组质粒,然后将野生型FHL2及其突变体与GAL4-DBD在框内融合,得到野生型FHL2及其突变体表达载体。将重组质粒转染到293T细胞中。Western blot结果显示,所有融合蛋白均有表达。利用gal4荧光素酶报告基因分析FHL2的转录激活特性,结果表明野生型FHL2在293T和MCF-7细胞中均具有激活活性。n端一半LIM结构域的缺失严重损害了FHL2刺激转录的能力。在c端缺乏LIM结构域的突变体完全失活,而在c端缺失两个LIM结构域则部分恢复了其刺激转录的能力。c端第二个LIM结构域的缺失没有改变FHL2的激活能力。这些结果表明,FHL2 c端最后一个LIM结构域对其转录激活功能至关重要,c端第二个LIM结构域可能是一个负调控区,但这种负调控依赖于最后一个LIM结构域。FHL2转录激活域的定位为进一步研究FHL2的各种功能奠定了坚实的基础。
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