非洲爪蟾snc-RNA基因主要位于te内,并在脊髓损伤后的再生和非再生阶段差异表达。

D. Araya, B. Valdebenito, Johany Peñailillo, J. Larraín, Gonzalo Riadi
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引用次数: 0

摘要

非洲爪蟾的早期发育阶段被称为再生(R)阶段,因为在这段时间里,它能够再生。在其蜕变为蛙类后,进入非再生阶段。据报道,在脊髓损伤后的各个阶段表达的基因库存在差异,并且在其时间上也存在差异。一个可能影响基因表达及其时间的分子因子是小的非编码rna (snc- rna)。为了深入了解snc- rna的作用,在这项工作中,我们旨在研究它们在R和NR阶段的差异表达及其在基因组区域的起源。我们对R期和NR期进行了小RNA测序和差异表达分析。大多数测序的snc-RNA具有高质量,其长度表明大多数属于小干扰RNA或微RNA类。平均而言,约5000万个序列中98%完全与野田鼠基因组一致,约45%为新的snc- rna。以snc-RNA的基因组定位为标准,进一步将snc-RNA分为2.238个家族:约49%的新snc-RNA位于TEs区。~53%的家族起源于基因(~33%在内含子区),~47%在基因间区。374种新的snc- rna被差异表达。289个来自te,其中250个位于基因间区,39个位于内含子区。这些结果,连同差异表达的基因,将有助于理解青蛙的脊髓再生过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Xenopus snc-RNA genes are predominantly located within TEs and are differentially expressed in regenerative and non-regenerative stages after spinal cord injury.
The early development stages of the frog Xenopus laevis are known as the regenerative (R) stage, because during that time, it is able to regenerate. After its metamorphosis into a frog, X. laevis goes into its non-regenerative (NR) stage. It has been reported that there are differences in the gene repertoire expressed at each stage after spinal cord injury, and also in its timing. One molecular agent that might influence gene expression and its timing are small non-coding RNAs (snc-RNAs). To gain insights into the role of snc-RNAs, in this work we aimed to investigate their differential expression between the R and the NR stages and their origins in genome regions. We have performed small RNA sequencing and differential expression analysis between the R and the NR stages. The majority of sequenced snc-RNAs have high quality, and their lengths suggest that the majority belong to the small interfering or, to the micro RNA class. In average, 98% of the ~50 million sequences completely aligned to X. laevis genome, and ~45% of them represent novel snc-RNAs. The snc-RNAs were further classified in 2.238 families, using as criteria their genomic location: ~49% of novel snc-RNA are in TEs regions. ~53% of families have their origins in genes (~33% in intronic regions) and ~47% in intergenic regions. 374 novel snc-RNAs are differentially expressed. 289 come from TEs, 250 of which are in intergenic regions and 39 are in intronic regions. These results, taken together with the differentially expressed genes, will help understanding the spinal cord regeneration process in frogs.
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