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作 者:童英[1] 李冰霞[1] 陈金辉[1] 刘正华[1] 郑康[1] 罗琛[2]
机构地区:[1]湖南师范大学生命科学学院,湖南长沙410081 [2]浙江大学生命科学学院,浙江杭州310058
出 处:《激光生物学报》2007年第4期418-423,共6页Acta Laser Biology Sinica
基 金:国家自然科学基金项目(30370696);国家"973"项目(2004CB117401)
摘 要:Vsx1是第一个在金鱼中发现的编码含有同源异型框(homeodomain)和CVC结构域蛋白的基因。该基因在胚胎发育的不同阶段在胚胎的不同区域和不同组织中表达,并已经证明它在视网膜视锥双极细胞的分化和正常功能的维持中具有重要作用。为了进一步研究该基因在不同发育阶段组织特异性表达的调节机制,实验用PCR方法分析了金鱼Vsx1的基因组结构和内含子多态性。结果表明:金鱼Vsx1基因由5个外显子和4个内含子组成,与斑马鱼、人、小鼠的Vsx1基因结构相同。4个内含子中,第一内含子有两种序列差异明显的类型,但第二、三、四内含子无明显差异。第一内含子的一种类型比另外一种类型多39个碱基,这39个碱基中包括了真核生物增强子的核心序列。这一观测结果提示金鱼Vsx1第一内含子可能与该基因的发育阶段特异性和组织特异性表达调节有关。同时,第一内含子序列的明显差异也为分析Vsx1不同等位基因或基因拷贝的表达活性,以及组织特异性表达调节方式提供了合适的探针序列。Visual system homeobox-1 ( Vsxl ) is a homeobox gene encoding a homeodomain and a CVC domain that was first cloned from an adult goldfish retinal library. This gene is expressed in different regions and tissues of the embryo during development. It plays a pivotal role in differentiation and maintenance of retinal bipolar cells. To study the regulatory mechanism of Vsxl expression, we analyzed the genomic structure and intron polymorphism of goldfish Vsxl by PCR. The gene was found to consist of five exons and four introns. The exon-intron structure is conserved among zebrafish Vsxl, mouse Vsxl and human Vsxl. Two obviously different categories were determined in the first intron of goldfish Vsxl, one has 39 base pairs, which contain a core sequence of eukaryote enhancer, more than the other. No significant divergence was detected in the other three intrans. The results suggest that the first intron of goldfish Vsxl may be associated with the expression regulatory of Vsxl, The significant polymorphism in the first intron of goldfish Vsxl also provides us with suitable probes to analyze expression levels of Vsxl at the same loci or different locus as well as the regulatory mechanism of Vsxl tissue-specific expression.
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