DNA shuffling method for generating estrogen receptor α and β chimeras in yeast

Jun Sun, John A. Katzenellenbogen, Huimin Zhao, Benita S. Katzenellenbogen

Research output: Contribution to journalArticle

Abstract

To facilitate our study of the molecular basis for the estrogen receptor (ER) subtype selectivity of novel ligands, we used DNA shuffling to construct chimeric ERs having ligand binding domains derived from both ERα and ERβ. The efficiency of chimera generation was low with traditional DNA shuffling protocols. Furthermore, ER ligand binding domain sequences lack convenient restriction sites for introducing chimeric ligand binding domain sequences into expression vectors. To overcome these problems, we developed a modified strategy whereby chimeric sequences were exclusively amplified from among the reassembled products from DNA shuffling using a special pair of PCR primers whose 3′ ends specifically match the α and β sequences, respectively, and whose 5′ ends match sequences outside the ERβ ligand binding domain. When chimeric ligand binding domain DNA sequences, amplified with these primers, were co-transformed into a yeast strain with a linearized expression vector for ERβ, an active expression vector was produced by homologous recombination. Twenty-two different crossover sites were found; most occurred when there was a stretch of eight or more identical base pairs in both sequences, and many were concentrated in the regions important for studying ligand binding and transactivation. This method should prove to be useful for generating chimeric gene products from parent templates that share relatively low sequence identity.

Original languageEnglish (US)
Pages (from-to)278-288
Number of pages11
JournalBioTechniques
Volume34
Issue number2
StatePublished - Feb 1 2003

ASJC Scopus subject areas

  • Biotechnology
  • Biochemistry, Genetics and Molecular Biology(all)

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