Species identification and authentification of human and rodent cell cultures using polymerase chain reaction analysis of vomeronasal receptor genes

被引:4
|
作者
Holder, M. J. [1 ]
Cooper, P. R. [1 ]
机构
[1] Univ Birmingham, Sch Dent, Birmingham B4 6NN, W Midlands, England
关键词
PCR; Vomeronasal receptors; Species specificity; Genomic DNA; CROSS-CONTAMINATION; ANIMAL-CELLS; LINES; DNA; AUTHENTICATION; PCR; ISOENZYME; IDENTITY;
D O I
10.1007/s10616-011-9394-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cell culture and the use of cell lines are routinely used in basic scientific research. It is therefore imperative for researchers to ensure the origin of the cell lines used and that they are routinely re-analysed for contamination and misidentification. Inter-species contamination is relatively frequent, and the most commonly used cell lines are of human, mouse and rat derivation. We have developed simple species specific primer assays based on genomic sequence differences in vomeronasal receptor gene family members to discriminate between human, mouse and rat DNA using standard agarose gel electrophoresis. Furthermore, these PCR assays are able to identify the species composition within an inter-species mixed population. This approach therefore provides a valuable tool to enable a rapid, simple and relatively inexpensive determination of the authentication and contamination of cell cultures.
引用
收藏
页码:553 / 558
页数:6
相关论文
共 50 条
  • [1] Species identification and authentification of human and rodent cell cultures using polymerase chain reaction analysis of vomeronasal receptor genes
    M. J. Holder
    P. R. Cooper
    Cytotechnology, 2011, 63 : 553 - 558
  • [2] Identification and verification of rodent cell lines by polymerase chain reaction
    Steube, Klaus G.
    Koelz, Anne-Leena
    Drexler, Hans G.
    CYTOTECHNOLOGY, 2008, 56 (01) : 49 - 56
  • [3] Identification and verification of rodent cell lines by polymerase chain reaction
    Klaus G. Steube
    Anne-Leena Koelz
    Hans G. Drexler
    Cytotechnology, 2008, 56 : 49 - 56
  • [4] Identification of Mycobacterium species in contaminated cultures by polymerase chain reaction
    Lima, DM
    Bollela, VR
    Jácomo, BJT
    Martinez, R
    da Fonseca, BAL
    CHEST, 2005, 127 (04) : 1283 - 1288
  • [5] DETECTION OF RODENT CORONAVIRUSES IN TISSUES AND CELL-CULTURES BY USING POLYMERASE CHAIN-REACTION
    HOMBERGER, FR
    SMITH, AL
    BARTHOLD, SW
    JOURNAL OF CLINICAL MICROBIOLOGY, 1991, 29 (12) : 2789 - 2793
  • [6] Detection and species identification of four human herpesviruses using polymerase chain reaction coupled with restriction endonuclease analysis
    Demkin, VV
    Kruglova, AI
    Nikolaeva, NP
    Yurchenko, JV
    JOURNAL OF VIROLOGICAL METHODS, 2002, 103 (02) : 121 - 128
  • [7] Multiplex polymerase chain reaction for rapid identification of mycobacterial species in liquid cultures.
    Ryang, DW
    Kim, SM
    Kee, SJ
    Shin, MG
    Shin, JH
    Suh, SP
    CLINICAL CHEMISTRY, 2000, 46 (06) : A204 - A204
  • [8] ANALYSIS OF T-CELL RECEPTOR TRANSCRIPTS USING THE POLYMERASE CHAIN-REACTION
    ROTH, ME
    LACY, MJ
    MCNEIL, LK
    KRANZ, DM
    BIOTECHNIQUES, 1989, 7 (07) : 746 - &
  • [9] IDENTIFICATION OF MUSCARINIC RECEPTOR SUBTYPES IN HUMAN EYE BY POLYMERASE CHAIN-REACTION
    GIL, DW
    BOGARDUS, AM
    WOLDEMUSSIE, E
    COCAPRADOS, M
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1991, 32 (04) : 1256 - 1256
  • [10] Identification of mycobacteria infecting fish to the species level using polymerase chain reaction and restriction enzyme analysis
    Talaat, AM
    Reimschuessel, R
    Trucksis, M
    VETERINARY MICROBIOLOGY, 1997, 58 (2-4) : 229 - 237