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First published online 23 December 2002
doi: 10.1242/jcs.00266
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Research Article |
subunit to negatively regulate haploid invasive growth


Brookdale Department of Molecular, Cell, and Developmental Biology, Mount
Sinai School of Medicine, New York, NY 10029, USA
* Present address: Servei de Cardiologia, Escala 1, planta 6, Hospital
Clínic de Barcelona, Villaroel 170, Barcelona 08036, Spain
Present address: Applied Biosystems, 35 Wiggins Avenue, Bedford, MA 01730,
USA
Author for correspondence (e-mail:
jeanne.hirsch{at}mssm.edu)
Accepted 11 November 2002
The yeast G
subunit Gpa2p and its coupled receptor Gpr1p
function in a signaling pathway that is required for the transition to
pseudohyphal and invasive growth. A two-hybrid screen using a constitutively
active allele of GPA2 identified the KRH1 gene as encoding a
potential binding partner of Gpa2p. Strains containing deletions of
KRH1 and its homolog KRH2 were hyper-invasive and displayed
a high level of expression of FLO11, a gene involved in pseudohyphal
and invasive growth. Therefore, KRH1 and KRH2 encode
negative regulators of the invasive growth pathway. Cells containing
krh1
krh2
mutations also displayed increased
sensitivity to heat shock and decreased sporulation efficiency, indicating
that Krh1p and Krh2p regulate multiple processes controlled by the cAMP/PKA
pathway. The krh1
krh2
mutations suppressed
the effect of a gpa2
mutation on FLO11 expression and
eliminated the effect of a constitutively active GPA2 allele on
induction of FLO11 and heat shock sensitivity, suggesting that Krh1p
and Krh2p act downstream of Gpa2p. The Sch9p kinase was not required for the
signal generated by deletion of KRH1 and KRH2; however, the
cAMP-dependent kinase Tpk2p was required for generation of this signal. These
results support a model in which activation of Gpa2p relieves the inhibition
exerted by Krh1p and Krh2p on components of the cAMP/PKA signaling
pathway.
Key words: GPA2, KRH1, KRH2, Kelch repeat
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