Literature DB >> 7866865

Inverse polymerase chain reaction. An efficient approach to cloning cDNA ends.

S H Huang1.   

Abstract

The conventional polymerase chain reaction (PCR) requires that DNA sequences at both ends of the region to be amplified be known. Inverse PCR (IPCR) and anchored PCR overcome this limitation and amplify flanking unknown DNA sequences by utilizing inverse amplification and a universal primer, respectively. The major advantage of IPCR is that two gene-specific primers are reserved for specific and efficient amplification of the unknown cDNA ends on the basis of a small stretch of known sequence. The protocol consists of five steps: reverse transcription, synthesis of second strand cDNA, circularization of double strand cDNA, reopen the circle DNA, and amplification of the inverse DNA fragment.

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Year:  1994        PMID: 7866865     DOI: 10.1007/BF02789286

Source DB:  PubMed          Journal:  Mol Biotechnol        ISSN: 1073-6085            Impact factor:   2.695


  23 in total

1.  Double stranded DNA sequencing as a choice for DNA sequencing.

Authors:  H Zhang; R Scholl; J Browse; C Somerville
Journal:  Nucleic Acids Res       Date:  1988-02-11       Impact factor: 16.971

2.  High-efficiency cloning of full-length cDNA; construction and screening of cDNA expression libraries for mammalian cells.

Authors:  H Okayama; M Kawaichi; M Brownstein; F Lee; T Yokota; K Arai
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

3.  First-strand cDNA synthesis primed with oligo(dT).

Authors:  M S Krug; S L Berger
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

4.  An efficient strategy for cloning 5' extremities of rare transcripts permits isolation of multiple 5'-untranslated regions of rat tryptophan hydroxylase mRNA.

Authors:  J Delort; J B Dumas; M C Darmon; J Mallet
Journal:  Nucleic Acids Res       Date:  1989-08-25       Impact factor: 16.971

5.  Message amplification phenotyping (MAPPing): a technique to simultaneously measure multiple mRNAs from small numbers of cells.

Authors:  C A Brenner; A W Tam; P A Nelson; E G Engleman; N Suzuki; K E Fry; J W Larrick
Journal:  Biotechniques       Date:  1989 Nov-Dec       Impact factor: 1.993

6.  In vitro synthesis of DNA complementary to rabbit reticulocyte 10S RNA.

Authors:  I M Verma; G F Temple; H Fan; D Baltimore
Journal:  Nat New Biol       Date:  1972-02-09

7.  Common RNA polymerase I, II, and III upstream elements in mouse 7SK gene locus revealed by the inverse polymerase chain reaction.

Authors:  I S Moon; M O Krause
Journal:  DNA Cell Biol       Date:  1991 Jan-Feb       Impact factor: 3.311

8.  Preparation of denatured plasmid templates for PCR amplification.

Authors:  E C Lau; Z Q Li; H C Slavkin
Journal:  Biotechniques       Date:  1993-03       Impact factor: 1.993

9.  Interaction of bacteriophage T4 RNA and DNA ligases in joining of duplex DNA at base-paired ends.

Authors:  A Sugino; H M Goodman; H L Heyneker; J Shine; H W Boyer; N R Cozzarelli
Journal:  J Biol Chem       Date:  1977-06-10       Impact factor: 5.157

10.  Sequence-specific cleavage of single-stranded DNA: oligodeoxynucleotide-EDTA X Fe(II).

Authors:  G B Dreyer; P B Dervan
Journal:  Proc Natl Acad Sci U S A       Date:  1985-02       Impact factor: 11.205

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  9 in total

1.  A novel chromodomain protein, pdd3p, associates with internal eliminated sequences during macronuclear development in Tetrahymena thermophila.

Authors:  M A Nikiforov; M A Gorovsky; C D Allis
Journal:  Mol Cell Biol       Date:  2000-06       Impact factor: 4.272

2.  Isolation of the 5'-end of plant genes from genomic DNA by TATA-box-based degenerate primers.

Authors:  Yanwu Guo; Lanqing Ma; Yunpeng Ji; Gaobin Pu; Benye Liu; Zhigao Du; Guofeng Li; Hechun Ye; Hong Wang
Journal:  Mol Biotechnol       Date:  2011-02       Impact factor: 2.695

3.  T-linker-specific ligation PCR (T-linker PCR): an advanced PCR technique for chromosome walking or for isolation of tagged DNA ends.

Authors:  Yan Yuanxin; An Chengcai; Li Li; Gu Jiayu; Tan Guihong; Chen Zhangliang
Journal:  Nucleic Acids Res       Date:  2003-06-15       Impact factor: 16.971

4.  Targeted Transcriptional Repression in Bacteria Using CRISPR Interference (CRISPRi).

Authors:  John S Hawkins; Spencer Wong; Jason M Peters; Ricardo Almeida; Lei S Qi
Journal:  Methods Mol Biol       Date:  2015

5.  CRISPR interference (CRISPRi) for sequence-specific control of gene expression.

Authors:  Matthew H Larson; Luke A Gilbert; Xiaowo Wang; Wendell A Lim; Jonathan S Weissman; Lei S Qi
Journal:  Nat Protoc       Date:  2013-10-17       Impact factor: 13.491

6.  Shoot-specific down-regulation of protein farnesyltransferase (alpha-subunit) for yield protection against drought in canola.

Authors:  Yang Wang; Michelle Beaith; Maryse Chalifoux; Jifeng Ying; Tina Uchacz; Carlene Sarvas; Rebecca Griffiths; Monika Kuzma; Jiangxin Wan; Yafan Huang
Journal:  Mol Plant       Date:  2009-01       Impact factor: 13.164

7.  NXT2 is required for embryonic heart development in zebrafish.

Authors:  Haigen Huang; Bo Zhang; Parvana A Hartenstein; Jau-nian Chen; Shuo Lin
Journal:  BMC Dev Biol       Date:  2005-03-24       Impact factor: 1.978

8.  Wristwatch PCR: A Versatile and Efficient Genome Walking Strategy.

Authors:  Lingqin Wang; Mengya Jia; Zhaoqin Li; Xiaohua Liu; Tianyi Sun; Jinfeng Pei; Cheng Wei; Zhiyu Lin; Haixing Li
Journal:  Front Bioeng Biotechnol       Date:  2022-04-12

9.  Characterization of bacterial operons consisting of two tubulins and a kinesin-like gene by the novel Two-Step Gene Walking method.

Authors:  Martin Pilhofer; Andreas Peter Bauer; Martina Schrallhammer; Lothar Richter; Wolfgang Ludwig; Karl-Heinz Schleifer; Giulio Petroni
Journal:  Nucleic Acids Res       Date:  2007-10-16       Impact factor: 16.971

  9 in total

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