Doukeris Christina E, Planchart Antonio
Department of Biology, Bates College, Lewiston, ME 04240.
Adv Biol Res (Rennes). 2007;1(1-2):1-16.
The identification of novel DNA sequence motifs potentially participating in the regulation of gene transcription is a difficult task due to the small size and relative simplicity of the sequences involved. One possible way of overcoming this difficulty is to examine the promoter region of genes with similar expression profiles. Parameters of interest include similar tissue and cell-type specificity and quantitatively similar levels of mRNA in wild-type backgrounds. Tcp10b and Tctex1 are genes exhibiting these properties in that both are expressed at similar levels in pachytene spermatocytes of male mouse germ cells with little to no expression elsewhere. An analysis of the promoter region of these genes has uncovered a novel 20-nucleotide motif perfectly conserved in both. We have characterized the binding properties of this motif and show that it is specifically recognized by a 43 kD nuclear protein. The complex is highly stable and exhibits strong specificity. Furthermore, results from analyzing the sequence of several vertebrate genomes for the presence of the motif are consistent with the existence of a novel motif in the vicinity of several hundred genes.
由于所涉及序列的规模小且相对简单,鉴定可能参与基因转录调控的新型DNA序列基序是一项艰巨的任务。克服这一困难的一种可能方法是检查具有相似表达谱的基因的启动子区域。感兴趣的参数包括相似的组织和细胞类型特异性以及野生型背景下定量相似的mRNA水平。Tcp10b和Tctex1是表现出这些特性的基因,因为它们在雄性小鼠生殖细胞的粗线期精母细胞中以相似水平表达,而在其他地方几乎不表达或不表达。对这些基因的启动子区域进行分析发现了一个在两者中完全保守的新型20核苷酸基序。我们已经表征了该基序的结合特性,并表明它被一种43 kD的核蛋白特异性识别。该复合物高度稳定并表现出很强的特异性。此外,分析几个脊椎动物基因组序列中该基序存在情况的结果与数百个基因附近存在新型基序的情况一致。