Selective Associations of Hormonal Steroids with Aminoacyl Transfer RNAs and Control of Protein Synthesis*

  1. Ruei-Chen Chin and
  2. Chev Kidson
  1. Department of Molecular Genetics, Institute of Hormone Biology, Syntex Research Center, Palo Alto, California 94034

Abstract

The hormonal steroids progesterone, estradiol, testosterone, and 5α-dihydrotestosterone bind to aminoacyl-tRNA, but not to deacylated tRNA, implying that a change in conformation of tRNA occurs on aminoacylation. Binding is restricted to a few tRNA species and depends on the structure of both tRNA and steroid. There is one binding site per aminoacyl-tRNA molecule, the specificity of which appears to depend on a restricted, single-stranded loop sequence and on the tRNA conformation. By binding to an aminoacyl-tRNA, a steroid can control polypeptide synthesis in a model in vitro system by inhibiting chain elongation under conditions where aminoacyl-tRNA concentration is rate-limiting.

Footnotes

  • Present address: Department of Biochemistry, University of Queensland, St. Lucia, Brisbane, Q.4067, Australia.

  • * This paper is No. 4 in a series, “Interactions of Hormonal Steroids with Nucleic Acids”. The preceding paper is ref. 3.

« Previous | Next Article »Table of Contents