Literature DB >> 11444048

Pattern- and growth-linked cell cycles in Drosophila development.

B A Edgar1, J Britton, A F de la Cruz, L A Johnston, D Lehman, C Martin-Castellanos, D Prober.   

Abstract

During Drosophila development the cell cycle is subject to diverse regulatory inputs. In embryos, cells divide in stereotypic patterns that correspond to the cell fate map. There is little cell growth during this period, and cell proliferation is regulated at G2/M transitions by patterned transcription of the Cdk1-activator, Cdc25/String. The string locus senses pattern information via a > 40 kb cis-regulatory region composed of many cell-type specific transcriptional enhancers. Later, in differentiated larval tissues, the cell cycle responds to nutrition via mechanisms that sense cellular growth. These larval cell cycles lack mitoses altogether, and are regulated at G/S transitions. Cells in developing imaginal discs exhibit a cycle that is regulated at both G1/S and G2/M transitions. G2/M progression in disc cells is regulated, as in the embryo, by string transcription and is thus influenced by the many transcription factors that interact with string's 'pattern-sensing' control region. G1/S progression in disc cells is controlled, at least in part, by factors that regulate cell growth such as Myc, Ras and phosphatidylinositol-3-kinase. Thus G1/S progression appears to be growth-coupled, much as in the larval endocycles. The dual control mechanism used by imaginal disc cells allows integration of diverse inputs which operate in both cell specification and cell metabolism.

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Year:  2001        PMID: 11444048     DOI: 10.1002/0470846666.ch2

Source DB:  PubMed          Journal:  Novartis Found Symp        ISSN: 1528-2511


  7 in total

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5.  Mutations in String/CDC25 inhibit cell cycle re-entry and neurodegeneration in a Drosophila model of Ataxia telangiectasia.

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6.  Myc localizes to histone locus bodies during replication in Drosophila.

Authors:  Kaveh Daneshvar; Abid Khan; Julie M Goodliffe
Journal:  PLoS One       Date:  2011-08-23       Impact factor: 3.240

7.  JNK-dependent cell cycle stalling in G2 promotes survival and senescence-like phenotypes in tissue stress.

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  7 in total

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