Literature DB >> 2463672

Polymerase chain reaction with single-sided specificity: analysis of T cell receptor delta chain.

E Y Loh1, J F Elliott, S Cwirla, L L Lanier, M M Davis.   

Abstract

In the polymerase chain reaction (PCR), two specific oligonucleotide primers are used to amplify the sequences between them. However, this technique is not suitable for amplifying genes that encode molecules where the 5' portion of the sequences of interest is not known, such as the T cell receptor (TCR) or immunoglobulins. Because of this limitation, a novel technique, anchored polymerase chain reaction (A-PCR), was devised that requires sequence specificity only on the 3' end of the target fragment. It was used to analyze TCR delta chain mRNA's from human peripheral blood gamma delta T cells. Most of these cells had a V delta gene segment not previously described (V delta 3), and the delta chain junctional sequences formed a discrete subpopulation compared with those previously reported.

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Year:  1989        PMID: 2463672     DOI: 10.1126/science.2463672

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  183 in total

1.  Identification of differentially expressed 5'-end mRNA variants by an improved RACE technique (PEETA).

Authors:  G Flouriot; H Brand; F Gannon
Journal:  Nucleic Acids Res       Date:  1999-08-01       Impact factor: 16.971

2.  Conservation of Babesia bovis small heat shock protein (Hsp20) among strains and definition of T helper cell epitopes recognized by cattle with diverse major histocompatibility complex class II haplotypes.

Authors:  Junzo Norimine; Juan Mosqueda; Guy H Palmer; Harris A Lewin; Wendy C Brown
Journal:  Infect Immun       Date:  2004-02       Impact factor: 3.441

3.  Sequence specific generation of a DNA panhandle permits PCR amplification of unknown flanking DNA.

Authors:  D H Jones; S C Winistorfer
Journal:  Nucleic Acids Res       Date:  1992-02-11       Impact factor: 16.971

4.  Sequence analyses of three immunoglobulin G anti-virus antibodies reveal their utilization of autoantibody-related immunoglobulin Vh genes, but not V lambda genes.

Authors:  D F Huang; T Olee; Y Masuho; Y Matsumoto; D A Carson; P P Chen
Journal:  J Clin Invest       Date:  1992-12       Impact factor: 14.808

5.  Major histocompatibility complex determinants select T-cell receptor alpha chain variable region dominance in a peptide-specific response.

Authors:  K Natarajan; D Burstyn; M Zauderer
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-01       Impact factor: 11.205

6.  Identification of novel human T-cell receptor V beta gene segments by the anchored-polymerase chain reaction.

Authors:  C Lunardi; C Marguerie; A K So
Journal:  Immunogenetics       Date:  1992       Impact factor: 2.846

7.  Ligation-anchored PCR: a simple amplification technique with single-sided specificity.

Authors:  A B Troutt; M G McHeyzer-Williams; B Pulendran; G J Nossal
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-15       Impact factor: 11.205

8.  Molecular cloning of human testicular angiotensin-converting enzyme: the testis isozyme is identical to the C-terminal half of endothelial angiotensin-converting enzyme.

Authors:  M R Ehlers; E A Fox; D J Strydom; J F Riordan
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

9.  Characterization of an enteropathogenic bovine calicivirus representing a potentially new calicivirus genus.

Authors:  J R Smiley; K O Chang; J Hayes; J Vinjé; L J Saif
Journal:  J Virol       Date:  2002-10       Impact factor: 5.103

10.  Redefining the Epstein-Barr virus-encoded nuclear antigen EBNA-1 gene promoter and transcription initiation site in group I Burkitt lymphoma cell lines.

Authors:  B C Schaefer; J L Strominger; S H Speck
Journal:  Proc Natl Acad Sci U S A       Date:  1995-11-07       Impact factor: 11.205

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