Affiliation:
1. Department of Biochemistry and Molecular Biology, Graduate School of Medicine, The University of Tokyo, Bunkyo-Ku, Tokyo 113-0033, Japan
Abstract
ABSTRACT
In the fission yeast
Schizosaccharomyces pombe
the
nrd1
+
gene encoding an RNA binding protein negatively regulates the onset of differentiation. Its biological role is to block differentiation by repressing a subset of the Ste11-regulated genes essential for conjugation and meiosis until the cells reach a critical level of nutrient starvation. By using the phenotypic suppression of the
S. pombe
temperature-sensitive
pat1
mutant that commits lethal haploid meiosis at the restrictive temperature, we have cloned
ROD1
, a functional homologue of
nrd1
+
, from rat and human cDNA libraries. Like
nrd1
+
,
ROD1
encodes a protein with four repeats of typical RNA binding domains, though its amino acid homology to Nrd1 is limited. When expressed in the fission yeast,
ROD1
behaves in a way that is functionally similar to
nrd1
+
, being able to repress Ste11-regulated genes and to inhibit conjugation upon overexpression.
ROD1
is predominantly expressed in hematopoietic cells or organs of adult and embryonic rat. Like
nrd1
+
for fission yeast differentiation, overexpressed
ROD1
effectively blocks both 12-
O
-tetradecanoyl phorbol-13-acetate-induced megakaryocytic and sodium butyrate-induced erythroid differentiation of the K562 human leukemia cells without affecting their proliferative ability. These results suggest a role for
ROD1
in differentiation control in mammalian cells. We discuss the possibility that a differentiation control system found in the fission yeast might well be conserved in more complex organisms, including mammals.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
83 articles.
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