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Trans-natural antisense transcripts including noncoding RNAs in 10 species: implications for expression regulation.

机译:包括10种物种的非编码RNA在内的反天然反义转录物:对表达调控的影响。

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摘要

Natural antisense transcripts are at least partially complementary to their sense transcripts. Cis-Sense/Antisense pairs (cis-SAs) have been extensively characterized and known to play diverse regulatory roles, whereas trans-Sense/Antisense pairs (trans-SAs) in animals are poorly studied. We identified long trans-SAs in human and nine other animals, using ESTs to increase coverage significantly over previous studies. The percentage of transcriptional units (TUs) involved in trans-SAs among all TUs was as high as 4.13%. Particularly 2896 human TUs (or 2.89% of all human TUs) were involved in 3327 trans-SAs. Sequence complementarities over multiple segments with predicted RNA hybridization indicated that some trans-SAs might have sophisticated RNA-RNA pairing patterns. One-fourth of human trans-SAs involved noncoding TUs, suggesting that many noncoding RNAs may function by a trans-acting antisense mechanism. TUs in trans-SAs were statistically significantly enriched in nucleic acid binding, ion/protein binding and transport and signal transduction functions and pathways; a significant number of human trans-SAs showed concordant or reciprocal expression pattern; a significant number of human trans-SAs were conserved in mouse. This evidence suggests important regulatory functions of trans-SAs. In 30 cases, trans-SAs were related to cis-SAs through paralogues, suggesting a possible mechanism for the origin of trans-SAs. All trans-SAs are available at http://trans.cbi.pku.edu.cn/.
机译:天然反义转录物与其有义转录物至少部分互补。顺式/反义对(cis-SAs)已被广泛表征,并已知具有多种调节作用,而动物反式/反义对(trans-SAs)的研究却很少。我们在人类和其他九种动物中鉴定出长反式SA,使用EST可以大大提高覆盖率,优于以往的研究。在所有翻译单元中,涉及反式SA的转录单元(TU)的百分比高达4.13%。特别是2896个人类TU(占所有人类TU的2.89%)参与了3327个反式SA。具有预测的RNA杂交的多个片段的序列互补性表明,某些反式SA可能具有复杂的RNA-RNA配对模式。人类反式SA的四分之一涉及非编码TU,这表明许多非编码RNA可能通过反式反义机制发挥作用。在统计上,反式SA中的TU在核酸结合,离子/蛋白质结合以及运输和信号转导功能和途径方面显着丰富。大量的人类反式SA显示出一致或相互表达的模式;大量的人类反式SA在小鼠中保守。该证据表明反式SA的重要调控功能。在30例病例中,反式SA通过旁系同源物与顺式SA相关,这表明反式SA起源的可能机制。所有trans-SA均位于http://trans.cbi.pku.edu.cn/。

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