首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >Stable intronic sequence RNA (sisRNA), a new class of noncoding RNA from the oocyte nucleus of Xenopus tropicalis
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Stable intronic sequence RNA (sisRNA), a new class of noncoding RNA from the oocyte nucleus of Xenopus tropicalis

机译:稳定的内含子序列RNA(sisRNA),来自热带非洲爪蟾卵母细胞核的新型​​非编码RNA

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摘要

To compare nuclear and cytoplasmic RNA from a single cell type, free of cross-contamination, we studied the oocyte of the frog Xenopus tropicalis, a giant cell with an equally giant nucleus. We isolated RNA from manually dissected nuclei and cytoplasm of mature oocytes and subjected it to deep sequencing. Cytoplasmic mRNA consisted primarily of spliced exons derived from ~6700 annotated genes. Nearly all of these genes were represented in the nucleus by intronic sequences. However, unspliced nascent transcripts were not detected. Inhibition of transcription or splicing for 1-2 d had little or no effect on the abundance of nuclear intronic sequences, demonstrating that they are unusually stable. RT-PCR analysis showed that these stable intronic sequences are transcribed from the coding strand and that a given intron can be processed into more than one molecule. Stable intronic sequence RNA (sisRNA) from the oocyte nucleus constitutes a new class of noncoding RNA. sisRNA is detectable by RT-PCR in samples of total RNA from embryos up to the mid-blastula stage, when zygotic transcription begins. Storage of sisRNA in the oocyte nucleus and its transmission to the developing embryo suggest that it may play important regulatory roles during oogenesis and/or early embryogenesis.
机译:为了比较没有交叉污染的单一细胞类型的核和细胞质RNA,我们研究了青蛙Xenopustropicis的卵母细胞,它是一个具有同样巨大核的巨大细胞。我们从人工解剖的成熟卵母细胞的细胞核和细胞质中分离出RNA,并对其进行了深度测序。细胞质mRNA主要由衍生自〜6700个带注释基因的剪接外显子组成。这些基因几乎全部由内含子序列表示在细胞核中。但是,未检测到未剪接的新生转录本。抑制转录或剪接1-2天对核内含子序列的丰度几乎没有影响,甚至没有影响,这表明它们异常稳定。 RT-PCR分析表明,这些稳定的内含子序列是从编码链转录而来的,给定的内含子可以被加工成一个以上的分子。来自卵母细胞核的稳定内含子序列RNA(sisRNA)构成了一类新的非编码RNA。当合子转录开始时,可​​以通过RT-PCR在从胚胎直至胚泡中期的总RNA样品中检测到sisRNA。 sisRNA在卵母细胞核中的存储及其向发育中胚胎的传播表明,它可能在卵子发生和/或早期胚胎发生过程中发挥重要的调节作用。

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