The Donnelly Centre, University of Toronto, Toronto, Ontario M5S 3E1, Canada; Department of Molecular Genetics, University of Toronto, Toronto, Ontario M5S 3E1, Canada;
The Donnelly Centre, University of Toronto, Toronto, Ontario M5S 3E1, Canada;
Genes Dev. 2016 Mar 1;30(5):594-609. doi: 10.1101/gad.276931.115.
In a previous analysis of 2300 mRNAs via whole-mount fluorescent in situ hybridization in cellularizing Drosophila embryos, we found that 70% of the transcripts exhibited some form of subcellular localization. To see whether this prevalence is unique to early Drosophila embryos, we examined ∼8000 transcripts over the full course of embryogenesis and ∼800 transcripts in late third instar larval tissues. The numbers and varieties of new subcellular localization patterns are both striking and revealing. In the much larger cells of the third instar larva, virtually all transcripts observed showed subcellular localization in at least one tissue. We also examined the prevalence and variety of localization mechanisms for >100 long noncoding RNAs. All of these were also found to be expressed and subcellularly localized. Thus, subcellular RNA localization appears to be the norm rather than the exception for both coding and noncoding RNAs. These results, which have been annotated and made available on a recompiled database, provide a rich and unique resource for functional gene analyses, some examples of which are provided.
在对细胞化果蝇胚胎中的 2300 个 mRNA 进行全胚胎荧光原位杂交的先前分析中,我们发现 70%的转录本表现出某种形式的亚细胞定位。为了确定这种普遍性是否仅存在于早期果蝇胚胎中,我们在胚胎发生的全过程中检查了大约 8000 个转录本,在晚期三龄幼虫组织中检查了大约 800 个转录本。新的亚细胞定位模式的数量和种类都引人注目且具有启发性。在三龄幼虫的较大细胞中,观察到的几乎所有转录本在至少一种组织中都显示出亚细胞定位。我们还检查了 >100 个长非编码 RNA 的定位机制的普遍性和多样性。所有这些都被发现表达并定位于亚细胞。因此,对于编码和非编码 RNA 来说,亚细胞 RNA 定位似乎是常态而不是例外。这些结果已被注释并在重新编译的数据库中提供,为功能基因分析提供了丰富而独特的资源,其中提供了一些示例。