首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Sox3: a transcription factor for Cyp19 expression in the frog Rana rugosa.
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Sox3: a transcription factor for Cyp19 expression in the frog Rana rugosa.

机译:Sox3:一种在蛙蛙蛙中Cyp19表达的转录因子。

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Cyp19 is expressed at a high level in the gonad of the female tadpole of the frog Rana rugosa during sex determination. To identify sequence elements important for expression of Cyp19, we isolated a genomic clone (approximately 40 kbp) carrying R. rugosa Cyp19 and analyzed the nucleotide sequence of the 5'-flanking region to search for potential transcription factor binding sites. Sox (SRY-related HMG box) protein and Sf1 binding sites were found in the ovary-specific promoter region of Cyp19. Because Sox3 is located on the sex chromosome in R. rugosa, we conducted the luciferase reporter assay in Xenopus A6 cells using the promoter region. Sox3 drove the reporter gene in the cells, but Sf1 did not. When sequential deletion of the 2.7 kbp Cyp19-promoter region was undertaken, a fragment spanning nucleotides -191 to +48 was sufficient to drive the transcription of the reporter gene. In site-directed mutagenesis, the binding site at -57 in the region was critical for Sox3 responsiveness. Sox3 lacking the HMG box had no ability to promote Cyp19 transcription. In addition, a chromatin immunoprecipitation (ChIP) assay showed that DNA fragments were enriched 8-fold, as determined by real-time PCR, when chromatin was immunoprecipitated with the anti-His antibody against His-tagged Sox3. The results, taken together, suggest that Sox3 activates Cyp19 transcription by its direct binding to the binding site of the Cyp19 promoter region. Sox3 appears to be a factor that directs indifferent gonads to develop into an ovary in R. rugosa.
机译:在性别确定过程中,Cyp19在青蛙蛙蛙的雌性the的性腺中高水平表达。为了鉴定对Cyp19表达重要的序列元件,我们分离了携带R. rugosa Cyp19的基因组克隆(约40 kbp),并分析了5'侧翼区的核苷酸序列以寻找潜在的转录因子结合位点。在Cyp19的卵巢特异性启动子区域发现了Sox(与SRY相关的HMG框)蛋白和Sf1结合位点。因为Sox3位于R. rugosa的性染色体上,所以我们在Xenopus A6细胞中使用启动子区域进行了荧光素酶报告基因检测。 Sox3在细胞中驱动了报告基因,而Sf1没有。当进行2.7kbp的Cyp19-启动子区的顺序缺失时,跨越-191至+48核苷酸的片段足以驱动报告基因的转录。在定点诱变中,该区域-57处的结合位点对于Sox3反应性至关重要。缺少HMG框的Sox3没有能力促进Cyp19转录。此外,染色质免疫沉淀(ChIP)分析表明,当染色质用抗His标记的Sox3的抗His抗体免疫沉淀时,通过实时PCR测定,DNA片段富集了8倍。在一起的结果表明,Sox3通过直接结合Cyp19启动子区域的结合位点来激活Cyp19转录。 Sox3似乎是引导无性生殖腺发育成皱纹杜鹃卵巢的一个因素。

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