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Short Technical ReportsOpen Accesscc iconby icon

Dicistronic LacZ and Alkaline Phosphatase Reporter Constructs Permit Simultaneous Histological Analysis of Expression from Multiple Transgenes

    Xue Li

    Mount Sinai School of Medicine, New York, NY, USA

    ,
    Weidong Wang

    Mount Sinai School of Medicine, New York, NY, USA

    &
    Thomas Lufkin

    *Address correspondence to Thomas Lufkin, Brookdale Center for Developmental and Molecular Biology, Mount Sinai School of Medicine - Box 1126, One Gustave L. Levy Place, New York, NY 10029-6574, USA. Internet:

    E-mail Address: lufkin@msvax.mssm.edu

    Mount Sinai School of Medicine, New York, NY, USA

    Published Online:https://doi.org/10.2144/97235st03

    We report here the development of convenient dicistronic transgenic markers for the rapid and efficient simultaneous analysis of transgene activity in transgenic mice. Two sensitive histological markers, the β-galactosidase (β-gal)-encoding lacZ gene and the human placental alkaline phosphatase (hpAP) gene, have been fused to the internal ribosome entry sequence (IRES) from the encephalomyocarditis virus, which directs efficient mRNA cap-independent entry of the translational apparatus in mammalian cells. The IRES permits efficient translation of either lacZ or hpAP when placed anywhere within transgene exonic sequences, including both 5′ and 3′ untranslated regions. In addition, the production of constructs for transgenic analysis of DNA regulatory elements is greatly facilitated with IRES-lacZ or IRES-hpAP, since the IRES relieves the need for complicated in-frame transgene protein fusions to produce a functional β-gal or hpAP protein.