Literature DB >> 8090203

Repression of growth-regulated G1 cyclin expression by cyclic AMP in budding yeast.

M D Baroni1, P Monti, L Alberghina.   

Abstract

A yeast cell becomes committed to the cell division cycle only if it grows to a critical size and reaches a critical rate of protein synthesis. The coordination between growth and division takes place at a control step during the G1 phase of the cell cycle called Start. It relies on the G1-specific cyclins encoded by CLN1, 2 and 3, which trigger Start through the activation of the Cdc28 protein kinase. In fact, the Cln cyclins are rate-limiting for Start execution and depend on growth. Here we report that the cyclic AMP signal pathway modulates the dependency of Cln cyclins on growth. In particular, more growth is required to trigger Start because CLN1 and CLN2 are repressed by the cAMP signal, thus explaining the previously observed cAMP-dependent increase of the critical size and critical rate of protein synthesis. Cln3 is not inhibited by the cAMP pathway and counteracts this mechanism by partially mediating the growth-dependent expression of other G1 cyclins.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8090203     DOI: 10.1038/371339a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  52 in total

1.  CLN3 expression is sufficient to restore G1-to-S-phase progression in Saccharomyces cerevisiae mutants defective in translation initiation factor eIF4E.

Authors:  P Danaie; M Altmann; M N Hall; H Trachsel; S B Helliwell
Journal:  Biochem J       Date:  1999-05-15       Impact factor: 3.857

2.  Evidence for control of nitrogen metabolism by a START-dependent mechanism in Saccharomyces cerevisiae.

Authors:  B A Bryan; E McGrew; Y Lu; M Polymenis
Journal:  Mol Genet Genomics       Date:  2003-11-27       Impact factor: 3.291

3.  Kinetic analysis of a molecular model of the budding yeast cell cycle.

Authors:  K C Chen; A Csikasz-Nagy; B Gyorffy; J Val; B Novak; J J Tyson
Journal:  Mol Biol Cell       Date:  2000-01       Impact factor: 4.138

4.  Grr1 of Saccharomyces cerevisiae is connected to the ubiquitin proteolysis machinery through Skp1: coupling glucose sensing to gene expression and the cell cycle.

Authors:  F N Li; M Johnston
Journal:  EMBO J       Date:  1997-09-15       Impact factor: 11.598

5.  Ran1 functions to control the Cdc10/Sct1 complex through Puc1.

Authors:  M Caligiuri; T Connolly; D Beach
Journal:  Mol Biol Cell       Date:  1997-06       Impact factor: 4.138

Review 6.  Topology and control of the cell-cycle-regulated transcriptional circuitry.

Authors:  Steven B Haase; Curt Wittenberg
Journal:  Genetics       Date:  2014-01       Impact factor: 4.562

7.  The transcription factor Swi4 is target for PKA regulation of cell size at the G1 to S transition in Saccharomyces cerevisiae.

Authors:  Loredana Amigoni; Sonia Colombo; Fiorella Belotti; Lilia Alberghina; Enzo Martegani
Journal:  Cell Cycle       Date:  2015-06-05       Impact factor: 4.534

8.  Phosphorylation of Cdc28 and regulation of cell size by the protein kinase CKII in Saccharomyces cerevisiae.

Authors:  G L Russo; C van den Bos ; A Sutton; P Coccetti; M D Baroni; L Alberghina; D R Marshak
Journal:  Biochem J       Date:  2000-10-01       Impact factor: 3.857

9.  Cell-cycle arrest and inhibition of G1 cyclin translation by iron in AFT1-1(up) yeast.

Authors:  C C Philpott; J Rashford; Y Yamaguchi-Iwai; T A Rouault; A Dancis; R D Klausner
Journal:  EMBO J       Date:  1998-09-01       Impact factor: 11.598

10.  The global transcriptional activator of Saccharomyces cerevisiae, Gcr1p, mediates the response to glucose by stimulating protein synthesis and CLN-dependent cell cycle progression.

Authors:  Kristine A Willis; Kellie E Barbara; Balaraj B Menon; Jason Moffat; Brenda Andrews; George M Santangelo
Journal:  Genetics       Date:  2003-11       Impact factor: 4.562

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.