Literature DB >> 2612767

Transition of starving Dictyostelium cells to differentiation phase at a particular position of the cell cycle.

Y Maeda1, T Ohmori, T Abe, F Abe, A Amagai.   

Abstract

The relationship between proliferation and differentiation in Dictyostelium discoideum Ax-2 was analyzed with reference to the cell-cycle position at the onset of starvation, using cells synchronized by temperature shift (11.5 degrees C-22.0 degrees C). To examine how far Ax-2 cells at any particular phase of the cell cycle are able to progress through the cycle in response to nutritional deprivation, we measured temporal changes in cell number and nuclearity after starvation. Nuclear DNA synthesis in synchronously developing cells was also monitored by pulse-labeling with [methyl-3H]thymidine. Increase in cell number and subsequent DNA synthesis occurred in cells just before mitosis (referred to as T0.5 cells and T1 cells; 0.5 h and 1 h after the shift-up from 11.5 degrees C to 22.0 degrees C respectively), but not in T3, T5, or T7 cells. When T1 cells were incubated for 6 h in the absence of external nutrients, they (T1 + 6 cells) exhibited developmental features similar to T7 cells, which most rapidly acquired chemotactic sensitivity to 3',5'-cyclic adenosine monophosphate (cAMP) and EDTA-resistant cohesiveness after starvation. Thus, it is quite likely that Ax-2 cells may progress through the cell cycle to a particular point (possibly the cell-cycle position of T7 cells), irrespective of the presence or absence of nutrients, and enter the differentiation phase from this point under conditions of nutritional deprivation. There was no difference in the ratio of prestalk to prespore cells in migratory pseudoplasmodia derived from cells that had been starved at other cell-cycle positions.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1989        PMID: 2612767     DOI: 10.1111/j.1432-0436.1989.tb00744.x

Source DB:  PubMed          Journal:  Differentiation        ISSN: 0301-4681            Impact factor:   3.880


  10 in total

1.  Transcriptional switch of the dia1 and impA promoter during the growth/differentiation transition.

Authors:  Shigenori Hirose; Taira Mayanagi; Catherine Pears; Aiko Amagai; William F Loomis; Yasuo Maeda
Journal:  Eukaryot Cell       Date:  2005-08

2.  Autonomous and nonautonomous regulation of axis formation by antagonistic signaling via 7-span cAMP receptors and GSK3 in Dictyostelium.

Authors:  G T Ginsburg; A R Kimmel
Journal:  Genes Dev       Date:  1997-08-15       Impact factor: 11.361

3.  Relevance of histone H1 kinase activity to the G2/M transition during the cell cycle ofDictyostelium discoideum.

Authors:  T Arakane; Y Maeda
Journal:  J Plant Res       Date:  1997-03       Impact factor: 2.629

4.  Prespore cell fate bias in G1 phase of the cell cycle in Dictyostelium discoideum.

Authors:  Guokai Chen; Adam Kuspa
Journal:  Eukaryot Cell       Date:  2005-10

5.  Calcium regulates the expression of a Dictyostelium discoideum asparaginyl tRNA synthetase gene.

Authors:  Jyoti K Jaiswal; Vidyanand Nanjundiah
Journal:  J Biosci       Date:  2003-12       Impact factor: 1.826

6.  Cloning, sequencing, and expression of the genomic DNA encoding the protein phosphatase cdc25 in Dictyostelium discoideum.

Authors:  T Mayanagi; Y Maeda; S Hirose; T Arakane; T Araki; A Amagai
Journal:  Dev Genes Evol       Date:  2004-09-04       Impact factor: 0.900

7.  AmpA protein functions by different mechanisms to influence early cell type specification and to modulate cell adhesion and actin polymerization in Dictyostelium discoideum.

Authors:  Hoa N Cost; Elizabeth F Noratel; Daphne D Blumberg
Journal:  Differentiation       Date:  2013-07-31       Impact factor: 3.880

8.  Intracellular ATP levels influence cell fates in Dictyostelium discoideum differentiation.

Authors:  Haruka Hiraoka; Tadashi Nakano; Satoshi Kuwana; Masashi Fukuzawa; Yasuhiro Hirano; Masahiro Ueda; Tokuko Haraguchi; Yasushi Hiraoka
Journal:  Genes Cells       Date:  2020-03-13       Impact factor: 1.891

9.  Control of cell differentiation by mitochondria, typically evidenced in dictyostelium development.

Authors:  Yasuo Maeda; Junji Chida
Journal:  Biomolecules       Date:  2013-11-11

10.  Specific growth suppression of human cancer cells by targeted delivery of Dictyostelium mitochondrial ribosomal protein S4.

Authors:  Junji Chida; Hikaru Araki; Yasuo Maeda
Journal:  Cancer Cell Int       Date:  2014-06-20       Impact factor: 5.722

  10 in total

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