P-122: The Effect of Beta Globin Intron on Human LH Hormone Expression in CHO Cells

نویسندگان

  • A Amiri-Yekta Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
  • A Zomorodi Pour Department of Molecular Medicine, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran
  • H Gourabi Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
  • M Mahdavi Nosrati Department of Biology, Faculty of Sciences, NourDanesh Institute of Higher Education, Meymeh, Isfahan, Iran
  • MH Sanati Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
  • N Fatemi Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
چکیده مقاله:

Background Luteinizing hormone (LH) is a heterodimeric glycoprotein composed of alpha and beta subunits.This hormone is secreted from the pituitary gland. LH, in women triggers Menstrual cycle and ovulation. In men, LH stimulates production of testosterone, which plays a specialized role in sperm production. Up to day, LH hormone have produced in different ways such as codon optimization and also in various cell lines. Between mammalian expression systems, Chinese hamster ovary (CHO) cells, due to rapid proliferation and post-translational modifications, are more common than other hosts. One way to increase gene expression is use of introns. Beta-globin intron is composed of 3 exons and 2 introns. Human beta globin gene is located on chromosome subband 11p15.5. In this study, the beta-globin gene intron-I was used to enhance the expression of LH hormone. The purpose of this study, was to investigate the effects of intron I beta globin gene on LH expression. MaterialsAndMethods The gene construct was made by PCR and Soeing-PCR techniques. Then, this structure was cloned into pVitro2-neo-mcs expression vector. Results In continuous, recombinant colonies were approved by colony PCR, digestion and sequencing. Conclusion In the future, gene construct will be transferred into CHO cells by electroporation technique and exmined the expression level of recombinant protein by SDS-page, Western blotting and ELISA methods.

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عنوان ژورنال

دوره 9  شماره 2

صفحات  94- 94

تاریخ انتشار 2015-09-01

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