首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Disease gene candidates revealed by expression profiling of retinal ganglion cell development.
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Disease gene candidates revealed by expression profiling of retinal ganglion cell development.

机译:通过视网膜神经节细胞发育的表达谱揭示的疾病候选基因。

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摘要

To what extent do postmitotic neurons regulate gene expression during development or after injury? We took advantage of our ability to highly purify retinal ganglion cells (RGCs) to profile their pattern of gene expression at 13 ages from embryonic day 17 through postnatal day 21. We found that a large proportion of RGC genes are regulated dramatically throughout their postmitotic development, although the genes regulated through development in vivo generally are not regulated similarly by RGCs allowed to age in vitro. Interestingly, we found that genes regulated by developing RGCs are not generally correlated with genes regulated in RGCs stimulated to regenerate their axons. We unexpectedly found three genes associated with glaucoma, optineurin, cochlin, and CYP1B1 (cytochrome P450, family 1, subfamily B, polypeptide 1), previously thought to be primarily expressed in the trabecular meshwork, which are highly expressed by RGCs and regulated through their development. We also identified several other RGC genes that are encoded by loci linked to glaucoma. The expression of glaucoma-linked genes by RGCs suggests that, at least in some cases, RGCs may be directly involved in glaucoma pathogenesis rather than indirectly involved in response to increased intraocular pressure. Consistent with this hypothesis, we found that CYP1B1 overexpression potentiates RGC survival.
机译:有丝分裂后神经元在发育过程中或损伤后在多大程度上调节基因表达?我们利用了高度纯化视网膜神经节细胞(RGC)的能力,以分析从胚胎第17天到出生后21天的13个年龄段的基因表达模式。我们发现,很大一部分RGC基因在有丝分裂后的整个发育过程中受到显着调控。 ,尽管通过体内发育调控的基因通常不受允许在体外老化的RGC的相似调控。有趣的是,我们发现受发育中的RGC调控的基因通常与受刺激再生其轴突的RGC中调控的基因不相关。我们意外地发现了与青光眼,optineurin,cochlin和CYP1B1相关的三个基因(细胞色素P450,家族1,亚家族B,多肽1),先前被认为主要在小梁网中表达,并由RGC高度表达并通过它们的调控发展。我们还确定了由其他与青光眼有关的基因座编码的其他RGC基因。 RGCs与青光眼相关基因的表达表明,至少在某些情况下,RGCs可能直接参与青光眼的发病机理,而不是间接参与对眼压升高的反应。与此假设相符,我们发现CYP1B1过表达增强RGC的生存。

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