Cloning of differentially expressed genes in highly and low metastatic rat osteosarcomas by a modified cDNA-AFLP method

Biochem Biophys Res Commun. 1999 Jul 22;261(1):35-40. doi: 10.1006/bbrc.1999.0997.

Abstract

To identify differentially expressed genes between highly and low metastatic rat transplantable osteosarcomas, we applied a modified AFLP (amplified fragment length polymorphisms) method for cDNA subtraction. The specific point of our modification is selective amplification using suppression PCR technique after restriction enzyme cutting. Our cDNA-AFLP gave high reproducibility (about 95%) in mRNA patterns and enabled us to clone four dominantly expressed genes in a highly metastatic tumor line. Three showed homology with known genes, encoding Ki-67, a proliferation-associated effective marker of malignancy, type IV collagen alpha-3, a major component of basement membrane, and KIAA77 for which the function is unknown. Although one fragment showed no database homology, we revealed a derivation from the rat homologue of the Drosophila melanogaster diaphanous gene (Dia) by cloning of longer cDNA. Dia genes, known to affect actin filament formation, are downstream effectors of Rho small GTPase. The results suggest that alterations in the expression of cytoskeletal protein, basement membrane elements, and proliferative markers may be important for metastasis of osteosarcomas.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Blotting, Northern
  • Cloning, Molecular / methods*
  • DNA, Complementary / genetics
  • Gene Expression Regulation, Neoplastic*
  • Genes / genetics
  • Molecular Sequence Data
  • Neoplasm Metastasis / genetics*
  • Neoplasm Transplantation
  • Nucleotides / genetics
  • Osteosarcoma / genetics*
  • Osteosarcoma / pathology
  • Osteosarcoma / secondary
  • Polymerase Chain Reaction / methods
  • Polymorphism, Restriction Fragment Length
  • Rats
  • Reproducibility of Results
  • Sequence Homology
  • Tumor Cells, Cultured

Substances

  • DNA, Complementary
  • Nucleotides