Affiliation:
1. Department of Molecular Genetics, National Institute of Genetics, Mishima, Shizuoka 411-8540, 1 and
2. Japan Science and Technology Corporation, Kawaguchi, Saitama 332-0012, 2 Japan
Abstract
ABSTRACT
Both the gene and the cDNA encoding the Rpb4 subunit of RNA polymerase II were cloned from the fission yeast
Schizosaccharomyces pombe
. The cDNA sequence indicates that Rpb4 consists of 135 amino acid residues with a molecular weight of 15,362. As in the case of the corresponding subunits from higher eukaryotes such as humans and the plant
Arabidopsis thaliana
, Rpb4 is smaller than RPB4 from the budding yeast
Saccharomyces cerevisiae
and lacks several segments, which are present in the
S. cerevisiae
RPB4 subunit, including the highly charged sequence in the central portion. The RPB4 subunit of
S. cerevisiae
is not essential for normal cell growth but is required for cell viability under stress conditions. In contrast,
S. pombe
Rpb4 was found to be essential even under normal growth conditions. The fraction of RNA polymerase II containing RPB4 in exponentially growing cells of
S. cerevisiae
is about 20%, but
S. pombe
RNA polymerase II contains the stoichiometric amount of Rpb4 even at the exponential growth phase. In contrast to the RPB4 homologues from higher eukaryotes, however,
S. pombe
Rpb4 formed stable hybrid heterodimers with
S. cerevisiae
RPB7, suggesting that
S. pombe
Rpb4 is similar, in its structure and essential role in cell viability, to the corresponding subunits from higher eukaryotes. However,
S. pombe
Rpb4 is closer in certain molecular functions to
S. cerevisiae
RPB4 than the eukaryotic RPB4 homologues.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
43 articles.
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