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通过II类限制性内切酶产生的3'端cDNA片段对整个mRNA群体进行描述。

Description of the entire mRNA population by a 3' end cDNA fragment generated by class IIS restriction enzymes.

作者信息

Kato K

机构信息

Okayama Cell Switching Project, ERATO, JRDC, Kyoto, Japan.

出版信息

Nucleic Acids Res. 1995 Sep 25;23(18):3685-90. doi: 10.1093/nar/23.18.3685.

DOI:10.1093/nar/23.18.3685
PMID:7478997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC307266/
Abstract

A novel means of recording the expression status of the total gene population is described. Digestion of cDNA by class IIS restriction enzymes produces a fragment with a poly (A) stretch and a 5' overhang with an unknown sequence. This fragment contains information such as the class IIS enzyme that cuts cDNA nearest to the poly (A) stretch, the sequence of the 5' overhang, and the size of the fragment. Expressed genes can be discriminated and displayed by the fragment as follows: (i) cut the cDNA with one class IIS restriction enzyme; (ii) ligate the digested cDNA to that from a pool of 64 biotinylated adaptors cohesive to all possible overhangs; (iii) digest by other two class IIS enzymes; (iv) recover the ligated molecules with streptavidin-coated paramagnetic beads; (v) perform PCR with the adaptor-primer and an anchored oligo-dT primer; (vi) separate the amplified fragments by denaturing polyacrylamide gel electrophoresis. Repeat the experiment with 64 adaptors, three enzymes and three anchored oligo-dT primers displays most of the expressed genes. Because redundancy is minimized, this technique is also ideal for generating tags for expressed genes, with which to construct a transcript map of the genome.

摘要

本文描述了一种记录全基因组表达状态的新方法。用II类限制性内切酶消化cDNA会产生一个带有poly(A)尾和未知序列5'突出端的片段。该片段包含诸如最靠近poly(A)尾切割cDNA的II类酶、5'突出端的序列以及片段大小等信息。表达的基因可通过该片段按以下方式进行区分和展示:(i) 用一种II类限制性内切酶切割cDNA;(ii) 将消化后的cDNA与64种生物素化接头的混合物连接,这些接头与所有可能的突出端互补;(iii) 用另外两种II类酶消化;(iv) 用链霉亲和素包被的顺磁珠回收连接的分子;(v) 用接头引物和锚定寡聚dT引物进行PCR;(vi) 通过变性聚丙烯酰胺凝胶电泳分离扩增片段。用64种接头、三种酶和三种锚定寡聚dT引物重复该实验可展示大多数表达的基因。由于冗余度最小化,该技术也是生成表达基因标签以构建基因组转录图谱的理想方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce80/307266/4cae97b30c13/nar00018-0086-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce80/307266/88c80cb1479a/nar00018-0085-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce80/307266/0f98cf906ef5/nar00018-0086-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce80/307266/4cae97b30c13/nar00018-0086-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce80/307266/88c80cb1479a/nar00018-0085-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce80/307266/0f98cf906ef5/nar00018-0086-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce80/307266/4cae97b30c13/nar00018-0086-b.jpg

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本文引用的文献

1
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Eur J Neurosci. 1990;2(8):704-711. doi: 10.1111/j.1460-9568.1990.tb00460.x.
2
Distribution and cloning of eukaryotic mRNAs by means of differential display: refinements and optimization.通过差异显示进行真核生物mRNA的分布与克隆:改进与优化
Nucleic Acids Res. 1993 Jul 11;21(14):3269-75. doi: 10.1093/nar/21.14.3269.
3
AmpliGrease: "hot start" PCR using petroleum jelly.AmpliGrease:使用凡士林的“热启动”聚合酶链式反应
Jun二聚化蛋白2(JDP2)是转录因子AP-1家族的成员,介导RANKL诱导的破骨细胞分化。
J Exp Med. 2003 Apr 21;197(8):1029-35. doi: 10.1084/jem.20021321.
4
An integrated computational and laboratory approach for selective amplification of mRNAs containing the adenylate uridylate-rich element consensus sequence.一种用于选择性扩增含有富含腺苷酸尿苷酸元件共有序列的mRNA的综合计算与实验室方法。
Genome Res. 2002 Jun;12(6):985-95. doi: 10.1101/gr.204902.
5
Molecular indexing of human genomic DNA.人类基因组DNA的分子索引
Nucleic Acids Res. 2001 Oct 1;29(19):E95. doi: 10.1093/nar/29.19.e95.
6
A critical evaluation of differential display as a tool to identify genes involved in legume nodulation: looking back and looking forward.对差异显示作为鉴定参与豆科植物结瘤基因工具的批判性评估:回顾与展望。
Nucleic Acids Res. 2001 Sep 1;29(17):3459-68. doi: 10.1093/nar/29.17.3459.
7
Expression profiling by iAFLP: A PCR-based method for genome-wide gene expression profiling.基于iAFLP的表达谱分析:一种用于全基因组基因表达谱分析的基于PCR的方法。
Genome Res. 1999 Dec;9(12):1305-12. doi: 10.1101/gr.9.12.1305.
8
A strategy for genome-wide gene analysis: integrated procedure for gene identification.一种全基因组基因分析策略:基因识别的整合程序。
Proc Natl Acad Sci U S A. 1998 Sep 29;95(20):11909-14. doi: 10.1073/pnas.95.20.11909.
9
Magnetic bead capture of cDNAs from double-stranded plasmid cDNA libraries.从双链质粒cDNA文库中进行磁珠捕获cDNA
Nucleic Acids Res. 1997 Aug 1;25(15):3183-5. doi: 10.1093/nar/25.15.3183.
10
Differential display of genome subsets containing specific interspersed repeats.包含特定散布重复序列的基因组亚群的差异显示
Proc Natl Acad Sci U S A. 1997 Apr 29;94(9):4548-53. doi: 10.1073/pnas.94.9.4548.
Biotechniques. 1994 Jan;16(1):42-3.
4
Non-cloning amplification of specific DNA fragments from whole genomic DNA digests using DNA 'indexers'.
Gene. 1994 Aug 5;145(2):163-9. doi: 10.1016/0378-1119(94)90001-9.
5
A simple and very efficient method for generating cDNA libraries.一种简单且非常有效的生成cDNA文库的方法。
Gene. 1983 Nov;25(2-3):263-9. doi: 10.1016/0378-1119(83)90230-5.
6
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Proc Natl Acad Sci U S A. 1989 Nov;86(22):8902-6. doi: 10.1073/pnas.86.22.8902.
7
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Nucleic Acids Res. 1990 Oct 11;18(19):5705-11. doi: 10.1093/nar/18.19.5705.
8
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Gene. 1991 Apr;100:13-26. doi: 10.1016/0378-1119(91)90345-c.
9
Complementary DNA sequencing: expressed sequence tags and human genome project.互补DNA测序:表达序列标签与人类基因组计划
Science. 1991 Jun 21;252(5013):1651-6. doi: 10.1126/science.2047873.
10
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Curr Opin Genet Dev. 1992 Jun;2(3):412-6. doi: 10.1016/s0959-437x(05)80151-0.