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PRE-1, a cis element sufficient to enhance cone- and rod- specific expression in differentiating zebrafish photoreceptors

机译:PRE-1,一种足以增强分化斑马鱼感光器中视锥和视杆特异性表达的顺式元件

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Background Appropriate transcriptional regulation is required for cone photoreceptor development and integrity. To date, only a few cis-regulatory elements that control cone photoreceptor-specific expression have been characterised. The alpha-subunit of cone transducin (TαC) is specifically expressed in cone photoreceptors and is required for colour vision. In order to better understand the molecular genetics controlling the initiation of cone photoreceptor-specific expression in vivo, we have utilised zebrafish to identify cis-regulatory elements in the upstream promoter region of the TαC gene. Results A 0.5 kb TαC promoter fragment is sufficient to direct cone-specific expression in transgenic larvae. Within this minimal promoter, we identify photoreceptor regulatory element-1 (PRE-1), a unique 41 bp sequence. PRE-1 specifically binds nuclear factors expressed in ocular tissue. PRE-1 is not required for cone-specific expression directed from a 2.5 kb TαC promoter. However, PRE-1-like sequences, with potential functional redundancy, are located in this 2.5 kb promoter. PRE-1-rho which has the highest sequence and structural homology to PRE-1 is located in the rhodopsin promoter. Surprisingly, PRE-1 and PRE-1-rho are functionally distinct. We demonstrate that PRE-1, but not PRE-1-rho, is sufficient to enhance expression from a heterologous UV cone promoter. PRE-1 is also sufficient to enhance expression from a heterologous rhodopsin promoter without altering its rod photoreceptor specificity. Finally, mutations in consensus E-box and Otx sites prevent PRE-1 from forming complexes with eye nuclear protein and enhancing photoreceptor expression. Conclusions PRE-1 is a novel cis-regulatory module that is sufficient to enhance the initiation of photoreceptor-specific gene expression in differentiating rod and cone photoreceptors.
机译:背景技术视锥感光细胞的发育和完整性需要适当的转录调节。迄今为止,仅表征了少数控制视锥感光细胞特异性表达的顺式调控元件。视锥转导蛋白(TαC)的α亚基在视锥感光器中特别表达,是彩色视觉所必需的。为了更好地了解在体内控制视锥光感受器特异性表达起始的分子遗传学,我们利用斑马鱼来鉴定TαC基因上游启动子区域的顺式调控元件。结果一个0.5 kb的TαC启动子片段足以指导转基因幼虫中视锥细胞的特异性表达。在这个最小的启动子内,我们确定了感光受体调控元件1(PRE-1),一个独特的41 bp序列。 PRE-1特异性结合眼组织中表达的核因子。对于来自2.5 kbTαC启动子的视锥细胞特异性表达,不需要PRE-1。但是,具有潜在功能冗余的PRE-1类序列位于此2.5 kb启动子中。在视紫红质启动子中与PRE-1具有最高序列和结构同源性的PRE-1-rho。令人惊讶的是,PRE-1和PRE-1-rho在功能上是不同的。我们证明PRE-1,但不是PRE-1-rho,足以增强从异源UV锥启动子的表达。 PRE-1也足以增强异源视紫红质启动子的表达而不会改变其杆感光受体的特异性。最后,共有E-box和Otx位点的突变可防止PRE-1与眼核蛋白形成复合物并增强感光细胞的表达。结论PRE-1是一种新型的顺式调控模块,足以增强分化杆和视锥感光细胞中感光细胞特异性基因表达的启动。

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