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本文引用的文献

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Poly(A) tail recognition by a viral RNA element through assembly of a triple helix.通过三聚体形成识别多聚(A)尾的病毒 RNA 元件。
Science. 2010 Nov 26;330(6008):1244-7. doi: 10.1126/science.1195858.
2
A role for TREX components in the release of spliced mRNA from nuclear speckle domains.TREX 组件在从核斑点域中释放剪接 mRNA 中的作用。
Nat Commun. 2010 Oct 19;1:97. doi: 10.1038/ncomms1103.
3
ATP is required for interactions between UAP56 and two conserved mRNA export proteins, Aly and CIP29, to assemble the TREX complex.ATP 是 UAP56 与 Aly 和 CIP29 这两种保守的 mRNA 输出蛋白相互作用组装 TREX 复合物所必需的。
Genes Dev. 2010 Sep 15;24(18):2043-53. doi: 10.1101/gad.1898610.
4
Distinct patterns of expression and evolution of intronless and intron-containing mammalian genes.内含子和外显子哺乳动物基因的表达和进化的不同模式。
Mol Biol Evol. 2010 Aug;27(8):1745-9. doi: 10.1093/molbev/msq086. Epub 2010 Apr 1.
5
"Cotranscriptionality": the transcription elongation complex as a nexus for nuclear transactions.“共转录性”:作为核内活动枢纽的转录延伸复合体
Mol Cell. 2009 Oct 23;36(2):178-91. doi: 10.1016/j.molcel.2009.09.018.
6
UIF, a New mRNA export adaptor that works together with REF/ALY, requires FACT for recruitment to mRNA.UIF,一种新的与 REF/ALY 共同作用的 mRNA 输出衔接蛋白,需要 FACT 才能被招募到 mRNA 上。
Curr Biol. 2009 Dec 1;19(22):1918-24. doi: 10.1016/j.cub.2009.09.041.
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Nuclear neighborhoods and gene expression.核邻域与基因表达。
Curr Opin Genet Dev. 2009 Apr;19(2):172-9. doi: 10.1016/j.gde.2009.02.007. Epub 2009 Mar 30.
8
Pre-mRNA processing reaches back to transcription and ahead to translation.前体信使核糖核酸(pre-mRNA)加工可追溯到转录阶段,并延伸至翻译阶段。
Cell. 2009 Feb 20;136(4):688-700. doi: 10.1016/j.cell.2009.02.001.
9
Cotranscriptional recruitment of the mRNA export factor Yra1 by direct interaction with the 3' end processing factor Pcf11.通过与3'端加工因子Pcf11直接相互作用,mRNA输出因子Yra1的共转录募集。
Mol Cell. 2009 Jan 30;33(2):215-26. doi: 10.1016/j.molcel.2008.12.007. Epub 2008 Dec 24.
10
Imaging and characterizing influenza A virus mRNA transport in living cells.对甲型流感病毒mRNA在活细胞中的转运进行成像与表征。
Nucleic Acids Res. 2008 Sep;36(15):4913-28. doi: 10.1093/nar/gkn475. Epub 2008 Jul 24.

天然无内含子的 mRNAs 的输出和稳定性需要特定的编码区序列和 TREX mRNA 输出复合物。

Export and stability of naturally intronless mRNAs require specific coding region sequences and the TREX mRNA export complex.

机构信息

Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Proc Natl Acad Sci U S A. 2011 Nov 1;108(44):17985-90. doi: 10.1073/pnas.1113076108. Epub 2011 Oct 18.

DOI:10.1073/pnas.1113076108
PMID:22010220
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3207654/
Abstract

A great deal is known about the export of spliced mRNAs, but little is known about the export of mRNAs encoded by human cellular genes that naturally lack introns. Here, we investigated the requirements for export of three naturally intronless mRNAs (HSPB3, IFN-α1, and IFN-β1). Significantly, we found that all three mRNAs are stable and accumulate in the cytoplasm, whereas size-matched random RNAs are unstable and detected only in the nucleus. A portion of the coding region confers this stability and cytoplasmic localization on the naturally intronless mRNAs and a cDNA transcript, which is normally retained in the nucleus and degraded. A polyadenylation signal, TREX mRNA export components, and the mRNA export receptor TAP are required for accumulation of the naturally intronless mRNAs in the cytoplasm. We conclude that naturally intronless mRNAs contain specific sequences that result in efficient packaging into the TREX mRNA export complex, thereby supplanting the splicing requirement for efficient mRNA export.

摘要

关于拼接 mRNA 的输出,人们已经了解很多,但对于天然缺乏内含子的人类细胞基因编码的 mRNA 的输出,人们知之甚少。在这里,我们研究了三种天然无内含子的 mRNA(HSPB3、IFN-α1 和 IFN-β1)的输出要求。重要的是,我们发现这三种 mRNA 都是稳定的,并在细胞质中积累,而大小匹配的随机 RNA 是不稳定的,只能在核内检测到。编码区的一部分赋予了这些天然无内含子的 mRNA 和 cDNA 转录本稳定性和细胞质定位,而 cDNA 转录本通常保留在核内并被降解。多聚腺苷酸化信号、 TREX mRNA 输出成分和 mRNA 输出受体 TAP 是将天然无内含子的 mRNA 在细胞质中积累所必需的。我们得出结论,天然无内含子的 mRNA 含有特定的序列,这些序列导致其有效地包装到 TREX mRNA 输出复合物中,从而取代了高效 mRNA 输出所需的拼接要求。