Cloning and sequencing for the largest subunit of Chinese hamster RNA polymerase II gene: identification of a mutation related to abnormal induction of sister chromatid exchanges

Gene. 1997 Jul 31;194(2):267-72. doi: 10.1016/s0378-1119(97)00204-7.

Abstract

In order to analyze the mutation sites related to abnormal induction of sister chromatid exchanges (SCEs) in the RNA polymerase II largest subunit (RpII LS) gene of the Chinese hamster CHO-KI cell mutant, we have completely sequenced the whole region of the RpII LS cDNAs obtained from normal and mutant cells. By comparing both sequences, a mutation that results in an amino acid (aa) change in the RpII LS gene was found. This aa change was Pro (CCC) to Ser (TCC) at position 1006. Multiple alignment for aa sequences of RpII LS from various species revealed that this Pro residue was highly conserved throughout the eukaryotes. Considering the differences in physico-chemical properties between Pro and Ser residues, the Pro-->Ser substitution may alter the RpII LS structure.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • CHO Cells
  • Cloning, Molecular
  • Cricetinae
  • Cricetulus
  • DNA, Complementary
  • Humans
  • Molecular Sequence Data
  • Point Mutation*
  • RNA Polymerase II / genetics*
  • Sequence Homology, Amino Acid
  • Sister Chromatid Exchange / genetics*

Substances

  • DNA, Complementary
  • RNA Polymerase II

Associated data

  • GENBANK/D87293
  • GENBANK/D87294