Literature DB >> 3803713

Phosphorylation changes associated with the early cell cycle in Xenopus eggs.

E Karsenti, R Bravo, M Kirschner.   

Abstract

Enucleated and nondividing amphibian eggs undergo cyclic changes in cell morphology and in the level of maturation promoting factor (MPF) with a period similar to the early cleavage cycle. We show here that there is a corresponding phosphorylation and dephosphorylation of specific proteins associated with this fundamental cell cycle. M-phase is associated with a general increase in phosphatase activity and specific phosphorylation of a small set of M-phase proteins, reflected in an increased stochiometry of phosphate and increased turnover. At the end of metaphase and correlated with a drop in MPF the phosphoproteins are rapidly lost. By microinjecting M-phase phosphoproteins into arrested interphase and metaphase eggs we could show that the specific M-phase phosphorylation was not due to specificity in phosphatase action. The ability to segregate synthesis from phosphorylation demonstrates that regulation is not on the level of synthesis of the M-phase proteins. Taken together these data suggest that regulation of kinase activity in M-phase in the face of general rapid phosphate turnover in the egg plays an important role in the regulation of the fundamental mitotic cycle.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3803713     DOI: 10.1016/0012-1606(87)90048-0

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  25 in total

1.  MAPK inactivation is required for the G2 to M-phase transition of the first mitotic cell cycle.

Authors:  A Abrieu; D Fisher; M N Simon; M Dorée; A Picard
Journal:  EMBO J       Date:  1997-11-03       Impact factor: 11.598

2.  Identification of novel M phase phosphoproteins by expression cloning.

Authors:  N Matsumoto-Taniura; F Pirollet; R Monroe; L Gerace; J M Westendorf
Journal:  Mol Biol Cell       Date:  1996-09       Impact factor: 4.138

3.  G2 arrest in Xenopus oocytes depends on phosphorylation of cdc25 by protein kinase A.

Authors:  Brian C Duckworth; Jennifer S Weaver; Joan V Ruderman
Journal:  Proc Natl Acad Sci U S A       Date:  2002-12-11       Impact factor: 11.205

4.  Genetic control of cell division patterns in the Drosophila embryo.

Authors:  B A Edgar; P H O'Farrell
Journal:  Cell       Date:  1989-04-07       Impact factor: 41.582

5.  Related proteins are phosphorylated at tyrosine in response to mitogenic stimuli and at meiosis.

Authors:  J A Cooper
Journal:  Mol Cell Biol       Date:  1989-07       Impact factor: 4.272

6.  Proteomics of phosphorylation and protein dynamics during fertilization and meiotic exit in the Xenopus egg.

Authors:  Marc Presler; Elizabeth Van Itallie; Allon M Klein; Ryan Kunz; Margaret L Coughlin; Leonid Peshkin; Steven P Gygi; Martin Wühr; Marc W Kirschner
Journal:  Proc Natl Acad Sci U S A       Date:  2017-11-28       Impact factor: 11.205

7.  Protein phosphatase 2A1 is the major enzyme in vertebrate cell extracts that dephosphorylates several physiological substrates for cyclin-dependent protein kinases.

Authors:  P Ferrigno; T A Langan; P Cohen
Journal:  Mol Biol Cell       Date:  1993-07       Impact factor: 4.138

8.  Tyrosine phosphorylation and activation of homologous protein kinases during oocyte maturation and mitogenic activation of fibroblasts.

Authors:  J Posada; J Sanghera; S Pelech; R Aebersold; J A Cooper
Journal:  Mol Cell Biol       Date:  1991-05       Impact factor: 4.272

9.  Mitosis-specific monoclonal antibody MPM-2 inhibits Xenopus oocyte maturation and depletes maturation-promoting activity.

Authors:  J Kuang; J Zhao; D A Wright; G F Saunders; P N Rao
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

10.  cdc25 is one of the MPM-2 antigens involved in the activation of maturation-promoting factor.

Authors:  J Kuang; C L Ashorn; M Gonzalez-Kuyvenhoven; J E Penkala
Journal:  Mol Biol Cell       Date:  1994-02       Impact factor: 4.138

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.