Human T-cell receptor V gene segment of alpha and beta families: A revised primer design strategy

被引:1
作者
Ch'ng, Angela Chiew Wen [1 ]
Chan, Soo Khim [1 ]
Ignatius, Joshua [2 ]
Lim, Theam Soon [1 ,3 ]
机构
[1] Univ Sains Malaysia, Inst Res Mol Med, George Town 11800, Malaysia
[2] Univ Warwick, Warwick Mfg Grp, Coventry, W Midlands, England
[3] Univ Sains Malaysia, Analyt Biochem Res Ctr, George Town 11800, Malaysia
关键词
polymerase chain reaction (PCR); phylogenetic tree; semi-qualitative analysis; T-cell receptor; V gene usage; MULTIPLE SEQUENCE ALIGNMENT; YEAST SURFACE-DISPLAY; DIRECTED EVOLUTION; DNA-POLYMERASE; PEPTIDE-MHC; PCR; AMPLIFICATION; FIDELITY; PROTEIN; LYMPHOCYTES;
D O I
10.1002/eji.201747328
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The application of human TCR in cancer immunotherapy has gained momentum with developments in tumor killing strategies using endogenous adaptive immune responses. The successful coverage of a diverse TCR repertoire is mainly attributed to the primer design of the human TCR V genes. Here, we present a refined primer design strategy of the human TCR V gene by clustering V gene sequence homolog for degenerate primer design based on the data from IMGT. The primers designed were analyzed and the PCR efficiency of each primer set was optimized. A total of 112 alpha and 160 beta sequences were aligned and clustered using a phylogram yielding 32 and 27 V gene primers for the alpha and beta family. The new primer set was able to provide 93.75% and 95.63% coverage for the alpha and beta family, respectively. A semi-qualitative approach using the designed primer set was able to provide a relative view of the TCR V gene diversity in different populations. Taken together, the new primers provide a more comprehensive coverage of the TCR gene diversity for improved TCR library generation and TCR V gene analysis studies.
引用
收藏
页码:1186 / 1199
页数:14
相关论文
共 69 条
  • [1] Abramoff MD., 2004, BIOPHOTONICS INT, V11, P36, DOI DOI 10.1201/9781420005615.AX4
  • [2] GAPDH as a housekeeping gene: analysis of GAPDH mRNA expression in a panel of 72 human tissues
    Barber, RD
    Harmer, DW
    Coleman, RA
    Clark, BJ
    [J]. PHYSIOLOGICAL GENOMICS, 2005, 21 (03) : 389 - 395
  • [3] BENNUN A, 1991, P NATL ACAD SCI USA, V88, P2466, DOI 10.1073/pnas.88.6.2466
  • [4] Quantitative ratio of primer pairs and annealing temperature affecting PCR products in duplex amplification
    Bercovich, D
    Regev, Z
    Ratz, T
    Luder, A
    Plotsky, Y
    Gruenbaum, Y
    [J]. BIOTECHNIQUES, 1999, 27 (04) : 762 - +
  • [5] Evolution of Vertebrate Immunity
    Boehm, Thomas
    [J]. CURRENT BIOLOGY, 2012, 22 (17) : R722 - R732
  • [6] Protocol for high-sensitivity/long linear-range spectrofluorimetric DNA quantification using ethidium bromide
    Bonasera, Veronica
    Alberti, Saverio
    Sacchetti, Andrea
    [J]. BIOTECHNIQUES, 2007, 43 (02) : 173 - +
  • [7] Primer sets for cloning the human repertoire of T cell Receptor Variable regions
    Boria, Ilenia
    Cotella, Diego
    Dianzani, Irma
    Santoro, Claudio
    Sblattero, Daniele
    [J]. BMC IMMUNOLOGY, 2008, 9 (1)
  • [8] CHA RS, 1993, PCR METH APPL, V3, pS18
  • [9] Comparative study of IgA VH3 gene usage in healthy TST- and TST+ population exposed to tuberculosis: deep sequencing analysis
    Chin, Siang Tean
    Ignatius, Joshua
    Suraiya, Siti
    Tye, Gee Jun
    Sarmiento, Maria E.
    Acosta, Armando
    Norazmi, Mohd Nor
    Lim, Theam Soon
    [J]. IMMUNOLOGY, 2015, 144 (02) : 302 - 311
  • [10] PCR fidelity of Pfu DNA polymerase and other thermostable DNA polymerases
    Cline, J
    Braman, JC
    Hogrefe, HH
    [J]. NUCLEIC ACIDS RESEARCH, 1996, 24 (18) : 3546 - 3551