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本文引用的文献

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Comprehensive discovery of endogenous Argonaute binding sites in Caenorhabditis elegans.全面发现秀丽隐杆线虫内源性 Argonaute 结合位点。
Nat Struct Mol Biol. 2010 Feb;17(2):173-9. doi: 10.1038/nsmb.1745. Epub 2010 Jan 10.
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WormBase: a comprehensive resource for nematode research.WormBase:线虫研究的综合资源。
Nucleic Acids Res. 2010 Jan;38(Database issue):D463-7. doi: 10.1093/nar/gkp952. Epub 2009 Nov 12.
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Deadenylation of maternal mRNAs mediated by miR-427 in Xenopus laevis embryos.非洲爪蟾胚胎中由miR-427介导的母体mRNA去腺苷酸化作用
RNA. 2009 Dec;15(12):2351-63. doi: 10.1261/rna.1882009. Epub 2009 Oct 23.
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Role of 5'- and 3'-untranslated regions of mRNAs in human diseases.信使核糖核酸的5'非翻译区和3'非翻译区在人类疾病中的作用。
Biol Cell. 2009 May;101(5):251-62. doi: 10.1042/BC20080104.
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Massively parallel sequencing of the polyadenylated transcriptome of C. elegans.秀丽隐杆线虫多聚腺苷酸化转录组的大规模平行测序。
Genome Res. 2009 Apr;19(4):657-66. doi: 10.1101/gr.088112.108. Epub 2009 Jan 30.
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MicroRNAs: target recognition and regulatory functions.微小RNA:靶标识别与调控功能
Cell. 2009 Jan 23;136(2):215-33. doi: 10.1016/j.cell.2009.01.002.
7
Metabolism and regulation of canonical histone mRNAs: life without a poly(A) tail.经典组蛋白mRNA的代谢与调控:无poly(A)尾的生命历程
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8
Transcriptome analysis for Caenorhabditis elegans based on novel expressed sequence tags.基于新表达序列标签的秀丽隐杆线虫转录组分析。
BMC Biol. 2008 Jul 8;6:30. doi: 10.1186/1741-7007-6-30.
9
Two distinct mechanisms generate endogenous siRNAs from bidirectional transcription in Drosophila melanogaster.在黑腹果蝇中,两种不同的机制从双向转录中产生内源性小干扰RNA。
Nat Struct Mol Biol. 2008 Jun;15(6):581-90. doi: 10.1038/nsmb.1438. Epub 2008 May 25.
10
UTRome.org: a platform for 3'UTR biology in C. elegans.UTRome.org:秀丽隐杆线虫3'非翻译区生物学研究平台。
Nucleic Acids Res. 2008 Jan;36(Database issue):D57-62. doi: 10.1093/nar/gkm946. Epub 2007 Nov 5.

秀丽隐杆线虫 3'UTR 景观。

The landscape of C. elegans 3'UTRs.

机构信息

Center for Genomics and Systems Biology, Department of Biology, New York University, 1009 Silver Center, New York, NY 10003, USA.

出版信息

Science. 2010 Jul 23;329(5990):432-5. doi: 10.1126/science.1191244. Epub 2010 Jun 3.

DOI:10.1126/science.1191244
PMID:20522740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3142571/
Abstract

Three-prime untranslated regions (3'UTRs) of metazoan messenger RNAs (mRNAs) contain numerous regulatory elements, yet remain largely uncharacterized. Using polyA capture, 3' rapid amplification of complementary DNA (cDNA) ends, full-length cDNAs, and RNA-seq, we defined approximately 26,000 distinct 3'UTRs in Caenorhabditis elegans for approximately 85% of the 18,328 experimentally supported protein-coding genes and revised approximately 40% of gene models. Alternative 3'UTR isoforms are frequent, often differentially expressed during development. Average 3'UTR length decreases with animal age. Surprisingly, no polyadenylation signal (PAS) was detected for 13% of polyadenylation sites, predominantly among shorter alternative isoforms. Trans-spliced (versus non-trans-spliced) mRNAs possess longer 3'UTRs and frequently contain no PAS or variant PAS. We identified conserved 3'UTR motifs, isoform-specific predicted microRNA target sites, and polyadenylation of most histone genes. Our data reveal a rich complexity of 3'UTRs, both genome-wide and throughout development.

摘要

真核生物信使 RNA(mRNA)的 3' 非翻译区(3'UTR)含有许多调节元件,但仍在很大程度上未被描述。通过 polyA 捕获、3' 快速 cDNA 末端扩增、全长 cDNA 和 RNA-seq,我们在秀丽隐杆线虫中定义了大约 26000 个独特的 3'UTR,这些 3'UTR 约占 18328 个经实验支持的蛋白质编码基因的 85%,并对大约 40%的基因模型进行了修订。替代的 3'UTR 异构体很常见,在发育过程中通常会有差异表达。平均 3'UTR 长度随着动物年龄的增长而减少。令人惊讶的是,在 13%的多聚腺苷酸化位点中没有检测到多聚腺苷酸化信号 (PAS),主要是在较短的替代异构体中。反式拼接(与非反式拼接相比)的 mRNA 具有更长的 3'UTR,并且通常不含 PAS 或变体 PAS。我们鉴定了保守的 3'UTR 基序、异构体特异性预测的 microRNA 靶位点以及大多数组蛋白基因的多聚腺苷酸化。我们的数据揭示了 3'UTR 在全基因组和整个发育过程中的丰富复杂性。