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Alternative polyadenylation produces multiple 3’ untranslated regions of odorant receptor mRNAs in mouse olfactory sensory neurons

机译:替代的聚腺苷酸化在小鼠嗅觉感觉神经元中产生多种3'未翻转的气味受体MRNA区域

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Odorant receptor genes constitute the largest gene family in mammalian genomes and this family has been extensively studied in several species, but to date far less attention has been paid to the characterization of their mRNA 3' untranslated regions (3'UTRs). Given the increasing importance of UTRs in the understanding of RNA metabolism, and the growing interest in alternative polyadenylation especially in the nervous system, we aimed at identifying the alternative isoforms of odorant receptor mRNAs generated through 3'UTR variation. We implemented a dedicated pipeline using IsoSCM instead of Cufflinks to analyze RNA-Seq data from whole olfactory mucosa of adult mice and obtained an extensive description of the 3'UTR isoforms of odorant receptor mRNAs. To validate our bioinformatics approach, we exhaustively analyzed the 3'UTR isoforms produced from 2 pilot genes, using molecular approaches including northern blot and RNA ligation mediated polyadenylation test. Comparison between datasets further validated the pipeline and confirmed the alternative polyadenylation patterns of odorant receptors. Qualitative and quantitative analyses of the annotated 3' regions demonstrate that 1) Odorant receptor 3'UTRs are longer than previously described in the literature; 2) More than 77% of odorant receptor mRNAs are subject to alternative polyadenylation, hence generating at least 2 detectable?3'UTR isoforms; 3) Splicing events in 3'UTRs are restricted to a limited subset of odorant receptor genes; and 4) Comparison between male and female data shows no sex-specific differences in odorant receptor 3'UTR isoforms. We demonstrated for the first time that odorant receptor genes are extensively subject to alternative polyadenylation. This ground-breaking change to the landscape of 3'UTR isoforms of Olfr mRNAs opens new avenues for investigating their respective functions, especially during the differentiation of olfactory sensory neurons.
机译:气味受体基因构成哺乳动物基因组中最大的基因家族,这个家庭已经在几种物种中进行了广泛研究,但迄今为止,他们的mRNA 3'未翻译地区的表征已经不那么注意(3'UTRS)。鉴于UTR在理解RNA代谢的情况下越来越重要,以及替代多腺苷酸的越来越多的兴趣,特别是在神经系统中,我们旨在鉴定通过3'UTR变异产生的气味受体MRNA的替代异构体。我们使用ISOSOM实现了专用管道,而不是Cufflinks,以分析来自成人小鼠的整个嗅觉粘膜的RNA-SEQ数据,并获得了对气味受体MRNA的3'UTR同种型的广泛描述。为了验证我们的生物信息学方法,我们彻底地分析了由2个试点基因产生的3'UTR同种型,使用包括Northern印迹和RNA连接介导的多腺苷酸化试验的分子方法。数据集之间的比较进一步验证了管道并确认了替代的气味受体的多腺苷酸化图案。注释的3'区域的定性和定量分析表明1)气味受体3'UTRS比在文献中的先前描述; 2)超过77%的气味受体MRNA经受替代的多腺苷酸化,因此产生至少2个可检测的β3'UTR同种型; 3)3'UTR中的剪接事件仅限于气味受体基因的有限子集; 4)男性和女性数据之间的比较显示出气味受体3'UTR同种型的性别特异性差异。我们首次证明了气味受体基因广泛受到替代多腺苷酸化的。这种接地变化为OLFR MRNA的3'UTR同种型的景观打开了新的途径,用于研究各自的功能,特别是在嗅觉感觉神经元的分化期间。

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