University of Wisconsin School of Medicine and Public Health, Department of Cell and Regenerative Biology, Madison, Wisconsin, United States of America.
PLoS One. 2012;7(9):e45009. doi: 10.1371/journal.pone.0045009. Epub 2012 Sep 11.
To investigate the importance of core promoter elements for tissue-specific transcription of RNA polymerase II genes, we examined testis-specific transcription in Drosophila melanogaster. Bioinformatic analyses of core promoter sequences from 190 genes that are specifically expressed in testes identified a 10 bp A/T-rich motif that is identical to the translational control element (TCE). The TCE functions in the 5' untranslated region of Mst(3)CGP mRNAs to repress translation, and it also functions in a heterologous gene to regulate transcription. We found that among genes with focused initiation patterns, the TCE is significantly enriched in core promoters of genes that are specifically expressed in testes but not in core promoters of genes that are specifically expressed in other tissues. The TCE is variably located in core promoters and is conserved in melanogaster subgroup species, but conservation dramatically drops in more distant species. In transgenic flies, short (300-400 bp) genomic regions containing a TCE directed testis-specific transcription of a reporter gene. Mutation of the TCE significantly reduced but did not abolish reporter gene transcription indicating that the TCE is important but not essential for transcription activation. Finally, mutation of testis-specific TFIID (tTFIID) subunits significantly reduced the transcription of a subset of endogenous TCE-containing but not TCE-lacking genes, suggesting that tTFIID activity is limited to TCE-containing genes but that tTFIID is not an obligatory regulator of TCE-containing genes. Thus, the TCE is a core promoter element in a subset of genes that are specifically expressed in testes. Furthermore, the TCE regulates transcription in the context of short genomic regions, from variable locations in the core promoter, and both dependently and independently of tTFIID. These findings set the stage for determining the mechanism by which the TCE regulates testis-specific transcription and understanding the dual role of the TCE in translational and transcriptional regulation.
为了研究核心启动子元件对于 RNA 聚合酶 II 基因组织特异性转录的重要性,我们研究了黑腹果蝇的睾丸特异性转录。通过对 190 个仅在睾丸中特异性表达的基因的核心启动子序列进行生物信息学分析,鉴定出一个 10bp 的 A/T 富含基序,该基序与翻译控制元件 (TCE) 相同。TCE 在 Mst(3)CGP mRNAs 的 5'非翻译区起抑制翻译的作用,并且在异源基因中也起调节转录的作用。我们发现,在具有聚焦起始模式的基因中,TCE 在仅在睾丸中特异性表达的基因的核心启动子中显著富集,但在其他组织中特异性表达的基因的核心启动子中则不然。TCE 位于核心启动子中的位置不同,在黑腹果蝇亚组物种中保守,但在更远缘的物种中则显著降低。在转基因果蝇中,含有 TCE 的短(300-400bp)基因组区域可指导报告基因的睾丸特异性转录。TCE 的突变显著降低但并未完全消除报告基因的转录,表明 TCE 对于转录激活很重要但不是必需的。最后,睾丸特异性 TFIID(tTFIID)亚基的突变显著降低了一组内源性含 TCE 但不含 TCE 的基因的转录,表明 tTFIID 活性仅限于含 TCE 的基因,但 tTFIID 不是含 TCE 基因的必需调节剂。因此,TCE 是一组仅在睾丸中特异性表达的基因的核心启动子元件。此外,TCE 在短基因组区域内、核心启动子的不同位置、以及依赖和独立于 tTFIID 的情况下调节转录。这些发现为确定 TCE 调节睾丸特异性转录的机制以及理解 TCE 在翻译和转录调节中的双重作用奠定了基础。