Previous Article | Next Article ![]()
Mol. Cell. Biol., 06 1996, 2585-2593, Vol 16, No. 6
ME Nickas and MP Yaffe
Yeast cells with mutations in BRO1 display phenotypes similar to those
caused by deletion of BCK1, a gene encoding a MEK kinase that functions in
a mitogen-activated protein kinase pathway mediating maintenance of cell
integrity. bro1 cells exhibit a temperature-sensitive growth defect that is
suppressed by the addition of osmotic stabilizers or Ca2+ to the growth
medium or by additional copies of the BCK1 gene. At permissive
temperatures, bro1 mutants are sensitive to caffeine and respond abnormally
to nutrient limitation. A null mutation in BRO1 is synthetically lethal
with null mutations in BCK1, MPK1, which encodes a mitogen-activated
protein kinase that functions downstream of Bck1p, or PKC1, a gene encoding
a protein kinase C homolog that activates Bck1p. Analysis of the isolated
BRO1 gene revealed that it encodes a novel, 97- kDa polypeptide which
contains a putative SH3 domain-binding motif and is homologous to a protein
of unknown function in Caenorhabditis elegans.
Copyright © 1996, American Society for Microbiology
BRO1, a novel gene that interacts with components of the Pkc1p-mitogen- activated protein kinase pathway in Saccharomyces cerevisiae
Department of Biology, University of California, San Diego, La Jolla 92093, USA.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»