Milash Brett, Gao Jingxia, Stevenson Tamara J, Son Jong-Hyun, Dahl Tiffanie, Bonkowsky Joshua L
Bioinformatics Shared Resource, Huntsman Cancer Institute, Salt Lake City, USA.
Department of Pediatrics, University of Utah, 295 Chipeta Way, 84108, Salt Lake City, UT, USA.
BMC Genomics. 2016 May 4;17:334. doi: 10.1186/s12864-016-2638-x.
Despite the fundamental biological importance and clinical relevance of characterizing the effects of chronic hypoxia exposure on central nervous system (CNS) development, the changes in gene expression from hypoxia are unknown. It is not known if there are unifying principles, properties, or logic in the response of the developing CNS to hypoxic exposure. Here, we use the small vertebrate zebrafish (Danio rerio) to study the effects of hypoxia on connectivity gene expression across development. We perform transcriptional profiling at high temporal resolution to systematically determine and then experimentally validate the response of CNS connectivity genes to hypoxia exposure.
We characterized mRNA changes during development, comparing the effects of chronic hypoxia exposure at different time-points. We focused on changes in expression levels of a subset of 1270 genes selected for their roles in development of CNS connectivity, including axon pathfinding and synapse formation. We found that the majority of CNS connectivity genes were unaffected by hypoxia. However, for a small subset of genes hypoxia significantly affected their gene expression profiles. In particular, hypoxia appeared to affect both the timing and levels of expression, including altering expression of interacting gene pairs in a fashion that would potentially disrupt normal function.
Overall, our study identifies the response of CNS connectivity genes to hypoxia exposure during development. While for most genes hypoxia did not significantly affect expression, for a subset of genes hypoxia changed both levels and timing of expression. Importantly, we identified that some genes with interacting proteins, for example receptor/ligand pairs, had dissimilar responses to hypoxia that would be expected to interfere with their function. The observed dysynchrony of gene expression could impair the development of normal CNS connectivity maps.
尽管表征慢性低氧暴露对中枢神经系统(CNS)发育的影响具有根本的生物学重要性和临床相关性,但低氧导致的基因表达变化尚不清楚。发育中的中枢神经系统对低氧暴露的反应是否存在统一的原则、特性或逻辑也不明确。在此,我们使用小型脊椎动物斑马鱼(Danio rerio)来研究低氧对整个发育过程中连接相关基因表达的影响。我们以高时间分辨率进行转录谱分析,以系统地确定并通过实验验证中枢神经系统连接相关基因对低氧暴露的反应。
我们表征了发育过程中的mRNA变化,比较了不同时间点慢性低氧暴露的影响。我们关注了1270个因其在中枢神经系统连接发育中的作用而被选择的基因子集的表达水平变化,这些作用包括轴突导向和突触形成。我们发现大多数中枢神经系统连接相关基因不受低氧影响。然而,对于一小部分基因,低氧显著影响了它们的基因表达谱。特别是,低氧似乎影响了表达的时间和水平,包括以可能破坏正常功能的方式改变相互作用基因对的表达。
总体而言,我们的研究确定了发育过程中中枢神经系统连接相关基因对低氧暴露的反应。虽然对于大多数基因低氧没有显著影响其表达,但对于一小部分基因,低氧改变了表达水平和时间。重要的是,我们发现一些具有相互作用蛋白的基因,例如受体/配体对,对低氧有不同的反应,这预计会干扰它们的功能。观察到的基因表达不同步可能会损害正常中枢神经系统连接图谱的发育。