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Molecular and Cellular Biology, March 2000, p. 2087-2097, Vol. 20, No. 6
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
ArgRII, a Component of the ArgR-Mcm1 Complex Involved in the
Control of Arginine Metabolism in Saccharomyces
cerevisiae, Is the Sensor of Arginine
Najet
Amar,
Francine
Messenguy,*
Mohamed
El
Bakkoury, and
Evelyne
Dubois
Institut de Recherches Microbiologiques J.-M.
Wiame and Laboratoire de Microbiologie de l'Université Libre
de Bruxelles, B-1070 Brussels, Belgium
Received 20 September 1999/Returned for modification 11 November
1999/Accepted 16 December 1999
Repression of arginine anabolic genes and induction of arginine
catabolic genes are mediated by a three-component protein complex,
interacting with specific DNA sequences in the presence of arginine.
Although ArgRI and Mcm1, two MADS-box proteins, and ArgRII, a zinc
cluster protein, contain putative DNA binding domains, alone they are
unable to bind the arginine boxes in vitro. Using purified glutathione
S-transferase fusion proteins, we demonstrate that ArgRI
and ArgRII1-180 or Mcm1 and ArgRII1-180 are able to reconstitute an
arginine-dependent binding activity in mobility shift analysis. Binding
efficiency is enhanced when the three recombinant proteins are present
simultaneously. At physiological concentration, the full-length ArgRII
is required to fulfill its functions; however, when ArgRII is
overexpressed, the first 180 amino acids are sufficient to interact
with ArgRI, Mcm1, and arginine, leading to the formation of an
ArgR-Mcm1-DNA complex. Several lines of evidence indicate that ArgRII
is the sensor of the effector arginine and that the binding site of
arginine would be the region downstream from the zinc cluster, sharing
some identity with the arginine binding domain of bacterial arginine repressors.
*
Corresponding author. Mailing address: Institut de
Recherches Microbiologiques J.-M. Wiame, 1 Ave. E. Gryzon, B-1070
Brussels, Belgium. Phone: 32-2-5267277. Fax: 32-2-5267273. E-mail:
FANARG{at}RESULB.ULB.AC.BE.
Molecular and Cellular Biology, March 2000, p. 2087-2097, Vol. 20, No. 6
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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