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Vol. 14, No. 23, pp. 2962-2975, December 1, 2000
1 Howard Hughes Medical Institute and 2 Department
of Biological Chemistry, University of Michigan Medical Center,
Ann Arbor, Michigan 48109-0650, USA
Diploid budding yeast exhibits two developmental programs in
response to nitrogen starvation, pseudohyphal growth, and sporulation. Here we show that both programs are repressed by activation of the
unfolded protein response (UPR), a stress-signal transduction pathway
responsible for induction of endoplasmic reticulum (ER)-resident chaperones when protein folding in the ER is impaired. Pseudohyphal growth was derepressed in ire1
/ire1
and
hac1
/hac1
strains. Activation of the UPR or
overexpression of the transcription factor Hac1ip, the
product of an unconventional splicing reaction regulated by the UPR,
was sufficient for repression of pseudohyphal growth and meiosis.
HAC1 splicing occurred in a nitrogen-rich environment but
ceased rapidly on nitrogen starvation. Further, addition of ammonium
salts to nitrogen-starved cells was sufficient to rapidly reactivate
HAC1 splicing. We propose that high translation rates in a
nitrogen-rich environment are coupled to limited protein unfolding in
the ER, thereby activating the UPR. An activated UPR then represses
pseudohyphal growth and meiosis. Nitrogen starvation slows translation
rates, allowing for more efficient folding of nascent polypeptide
chains, down-regulation of the UPR, and subsequent derepression of
pseudohyphal growth and meiosis. These findings significantly broaden
the range of physiological functions of the UPR and define a role for
the UPR in nitrogen sensing.
[Key Words: unfolded protein response; pseudohyphal growth; meiosis; sporulation; nitrogen sensing; translation]
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