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Molecular and Cellular Biology, January 1999, p. 817-825, Vol. 19, No. 1
Department of Molecular Biology, Princeton
University, Princeton, New Jersey 08544-1014
Received 23 July 1998/Returned for modification 16 September
1998/Accepted 5 October 1998
Kar4p is a transcription factor in Saccharomyces
cerevisiae that is required for the expression of
karyogamy-specific genes during mating, for the efficient transit from
G1 during mitosis, and for essential functions during
meiosis. Kar4p exists in two forms: a constitutive slower-migrating
form, which predominates during vegetative growth, and a
faster-migrating form, which is highly induced by mating pheromone.
Transcript mapping of KAR4 revealed that the constitutive
mRNA was initiated upstream of two in-frame ATG initiation codons,
while the major inducible mRNA originated between them. Thus, the two
forms of Kar4p are derived from the translation of alternative
transcripts, which possess different AUG initiation codons.
Site-directed mutations were constructed to inactivate one or the other
of the initiation codons, allowing the expression of the two Kar4p
forms separately. At normal levels of expression, the constitutive form
of Kar4p did not support wild-type levels of mating. However, the two
forms of Kar4p could also be expressed separately from the regulatable GAL1 promoter, and no functional difference was detected
when they were expressed at equivalent levels. Pulse-chase experiments showed that the induced form of Kar4p was highly expressed and stable
during mating but rapidly turned over in vegetative cells. In contrast,
the constitutively expressed longer form showed the same rate of
turnover regardless of the growth condition. Furthermore, overexpression of either form of Kar4p in vegetative cells was toxic.
Thus, the elaborate regulation of the two forms of Kar4p at the levels
of transcription, translation, and protein turnover reflects the
requirement for high levels of the protein during mating and for low
levels during the subsequent phases of the cell cycle.
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Copyright © 1999, American Society for Microbiology. All rights reserved.
The Two Forms of Karyogamy Transcription Factor
Kar4p Are Regulated by Differential Initiation of Transcription,
Translation, and Protein Turnover

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Corresponding author. Mailing address: Department of
Molecular Biology, Princeton University, Princeton, NJ 08544-1014. Phone: (609) 258-2804. Fax: (609) 258-6175. E-mail:
mrose{at}molbio.princeton.edu.
Present address: Harvard Medical School, Boston, MA 02115.
Present address: Merck & Co., Inc., Rahway, NJ 07065.
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