
Cloning and sequence determination of theSchizosaccharomyces pombe rpb2 gene encoding the subunit 2 of RNA polymerase II
Author(s) -
Makiko Kawagishi,
M Yamagishi,
Akira Ishihama
Publication year - 1993
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/21.3.469
Subject(s) - biology , schizosaccharomyces pombe , schizosaccharomyces , complementary dna , genetics , nucleic acid sequence , intron , microbiology and biotechnology , sequence analysis , gene , genomic dna , coding region , saccharomyces cerevisiae
The gene, rpb2, encoding the second largest subunit, subunit 2, of RNA polymerase II has been cloned from Schizosaccharomyces pombe using the corresponding gene, RPB2, of Saccharomyces cerevisiae as a probe for cross-hybridization. We have determined the complete nucleotide sequence of rpb2, and parts of the PCR-amplified rpb2 cDNA. The predicted coding sequence of a polypeptide of 1210 amino acid residues with a calculated molecular weight of 138 kilodaltons was interrupted by a short intron. The overall amino acid sequence homology of the S. pombe subunit 2 is 68, 62 and 62% with the corresponding protein from S. cerevisiae, D. melanogaster and H. sapiens, respectively. Southern analysis of the genomic DNA digested with various restriction enzymes showed that rpb2 was present as a single copy in the S. pombe genome. Northern analysis showed that the transcript of rpb2 was about 4 kb in length.