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Loss of cone cyclic nucleotide-gated channel leads to alterations in light response modulating system and cellular stress response pathways: a gene expression profiling study

机译:锥环核苷酸门控通道的丢失导致光反应调节系统和细胞应激反应途径的改变:一项基因表达谱研究

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摘要

The cone photoreceptor cyclic nucleotide-gated (CNG) channel is essential for central and color vision and visual acuity. Mutations in the channel subunits CNGA3 and CNGB3 are associated with achromatopsia and cone dystrophy. We investigated the gene expression profiles in mouse retina with CNG channel deficiency using whole genome expression microarrays. As cones comprise only 2 to 3% of the total photoreceptor population in the wild-type mouse retina, the mouse lines with CNG channel deficiency on a cone-dominant background, i.e. Cnga3−/−/Nrl−/− and Cngb3−/−/Nrl−/− mice, were used in our study. Comparative data analysis revealed a total of 105 genes altered in Cnga3−/−/Nrl−/− and 92 in Cngb3−/−/Nrl−/− retinas, relative to Nrl−/− retinas, with 27 genes changed in both genotypes. The differentially expressed genes primarily encode proteins associated with cell signaling, cellular function maintenance and gene expression. Ingenuity pathway analysis (IPA) identified 26 and 9 canonical pathways in Cnga3−/−/Nrl−/− and Cngb3−/−/Nrl−/− retinas, respectively, with 6 pathways being shared. The shared pathways include phototransduction, cAMP/PKA-mediated signaling, endothelin signaling, and EIF2/endoplasmic reticulum (ER) stress, whereas the IL-1, CREB, and purine metabolism signaling were found to specifically associate with Cnga3 deficiency. Thus, CNG channel deficiency differentially regulates genes that affect cell processes such as phototransduction, cellular survival and gene expression, and such regulations play a crucial role(s) in the retinal adaptation to impaired cone phototransduction. Though lack of Cnga3 and Cngb3 shares many common pathways, deficiency of Cnga3 causes more significant alterations in gene expression. This work provides insights into how cones respond to impaired phototransduction at the gene expression levels.
机译:视锥细胞环状环状核苷酸门控(CNG)通道对于中央视觉和彩色视觉以及视敏度至关重要。通道亚基CNGA3和CNGB3的突变与色盲和视锥细胞营养不良有关。我们使用全基因组表达微阵列研究了CNG通道不足的小鼠视网膜中的基因表达谱。由于视锥细胞仅占野生型小鼠视网膜总感光细胞总数的2%至3%,因此在视锥细胞显性背景下具有CNG通道缺失的小鼠品系,即Cnga3 -// / Nrl <在我们的研究中使用了sup>-/-和Cngb3 -/- / Nrl -/-小鼠。比较数据分析显示,共有105个基因在Cnga3 -/- / Nrl -/-中发生了改变,在Cngb3 -/- / Nrl中发生了92个改变。相对于Nrl -/-视网膜,-/-视网膜具有两种基因型,其中27个基因发生了改变。差异表达的基因主要编码与细胞信号转导,细胞功能维持和基因表达相关的蛋白质。独创性途径分析(IPA)在Cnga3 -// / Nrl -/-和Cngb3 -/- / Nrl中确定了26和9个经典途径-/-视网膜分别具有6条路径。共有的途径包括光转导,cAMP / PKA介导的信号传导,内皮素信号传导和EIF2 /内质网(ER)应激,而IL-1,CREB和嘌呤代谢信号传导被发现与Cnga3缺乏症特别相关。因此,CNG通道缺乏差异性地调节影响细胞过程的基因,例如光转导,细胞存活和基因表达,并且这种调节在视网膜对视锥细胞光传导受损的适应中起着至关重要的作用。尽管缺乏Cnga3和Cngb3共有许多常见途径,但Cnga3的缺乏会导致基因表达发生更大的改变。这项工作提供了有关视锥细胞如何在基因表达水平上响应受损的光转导的见解。

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