Studies of the strand-annealing activity of mammalian hnRNP complex protein A1

Biochemistry. 1990 Dec 4;29(48):10717-22. doi: 10.1021/bi00500a001.

Abstract

A1 is a major core protein of the mammalian hnRNP complex, and as a purified protein of approximately 34 kDa, A1 is a strong single-stranded nucleic acid binding protein. Several lines of evidence suggest that the protein is organized in discrete domains consisting of an N-terminal segment of approximately 22 kDa and a C-terminal segment of approximately 12 kDa. Each of these domains as a purified fragment is capable of binding to both ssDNA and RNA. We report here that A1 and its C-terminal domain fragment are capable of potent strand-annealing activity for base-pair complementary single-stranded polynucleotides of both RNA and DNA. This effect is not stimulated by ATP. Compared with A1 and the C-terminal fragment, the N-terminal domain fragment has negligible annealing activity. These results indicate that A1 has biochemical activity consistent with a strand-annealing role in relevant reactions, such as pre-mRNA splicing.

MeSH terms

  • Animals
  • Bacteriophage phi X 174
  • DNA / metabolism
  • DNA, Single-Stranded / metabolism*
  • DNA, Viral / metabolism
  • DNA-Binding Proteins / metabolism*
  • Escherichia coli / metabolism
  • Heterogeneous Nuclear Ribonucleoprotein A1
  • Heterogeneous-Nuclear Ribonucleoprotein Group A-B*
  • Heterogeneous-Nuclear Ribonucleoproteins
  • Molecular Weight
  • Nucleic Acid Hybridization
  • Peptide Fragments / metabolism
  • RNA / metabolism*
  • Rats
  • Rec A Recombinases / metabolism
  • Ribonucleoproteins / analysis*

Substances

  • DNA, Single-Stranded
  • DNA, Viral
  • DNA-Binding Proteins
  • Heterogeneous Nuclear Ribonucleoprotein A1
  • Heterogeneous-Nuclear Ribonucleoprotein Group A-B
  • Heterogeneous-Nuclear Ribonucleoproteins
  • Peptide Fragments
  • Ribonucleoproteins
  • RNA
  • DNA
  • Rec A Recombinases