Literature DB >> 11583582

S-phase-specific expression of the Mad3 gene in proliferating and differentiating cells.

E J Fox1, S C Wright.   

Abstract

The Myc/Max/Mad transcription factor network plays a central role in the control of cellular proliferation, differentiation and apoptosis. In order to elucidate the biological function of Mad3, we have analysed the precise temporal patterns of Mad3 mRNA expression during the cell cycle and differentiation in cultured cells. We show that Mad3 is induced at the G1/S transition in proliferating cells; expression persists throughout S-phase, and then declines as cells pass through G2 and mitosis. The expression pattern of Mad3 is coincident with that of Cdc2 throughout the cell cycle. In contrast, the expression of Mad3 during differentiation of cultured mouse erythroleukemia cells shows two transient peaks of induction. The first of these occurs at the onset of differentiation, and does not correlate with the S-phase of the cell cycle, whereas the second is coincident with the S-phase burst that precedes the terminal stages of differentiation. Our results therefore suggest that Mad3 serves a cell-cycle-related function in both proliferating and differentiating cells, and that it may also have a distinct role at various stages of differentiation.

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Year:  2001        PMID: 11583582      PMCID: PMC1222154          DOI: 10.1042/0264-6021:3590361

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  63 in total

1.  Myc and Max associate in vivo.

Authors:  E M Blackwood; B Lüscher; R N Eisenman
Journal:  Genes Dev       Date:  1992-01       Impact factor: 11.361

2.  The essential cofactor TRRAP recruits the histone acetyltransferase hGCN5 to c-Myc.

Authors:  S B McMahon; M A Wood; M D Cole
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

3.  Mad: a heterodimeric partner for Max that antagonizes Myc transcriptional activity.

Authors:  D E Ayer; L Kretzner; R N Eisenman
Journal:  Cell       Date:  1993-01-29       Impact factor: 41.582

4.  max encodes a sequence-specific DNA-binding protein and is not regulated by serum growth factors.

Authors:  S Berberich; N Hyde-DeRuyscher; P Espenshade; M Cole
Journal:  Oncogene       Date:  1992-04       Impact factor: 9.867

Review 5.  MYC oncogenes and human neoplastic disease.

Authors:  C E Nesbit; J M Tersak; E V Prochownik
Journal:  Oncogene       Date:  1999-05-13       Impact factor: 9.867

6.  Binding of myc proteins to canonical and noncanonical DNA sequences.

Authors:  T K Blackwell; J Huang; A Ma; L Kretzner; F W Alt; R N Eisenman; H Weintraub
Journal:  Mol Cell Biol       Date:  1993-09       Impact factor: 4.272

7.  Transcriptional activation by the human c-Myc oncoprotein in yeast requires interaction with Max.

Authors:  B Amati; S Dalton; M W Brooks; T D Littlewood; G I Evan; H Land
Journal:  Nature       Date:  1992-10-01       Impact factor: 49.962

8.  Transcriptional activities of the Myc and Max proteins in mammalian cells.

Authors:  L Kretzner; E M Blackwood; R N Eisenman
Journal:  Curr Top Microbiol Immunol       Date:  1992       Impact factor: 4.291

9.  Mxi1, a protein that specifically interacts with Max to bind Myc-Max recognition sites.

Authors:  A S Zervos; J Gyuris; R Brent
Journal:  Cell       Date:  1993-01-29       Impact factor: 41.582

10.  Cell cycle regulation of the human cdc2 gene.

Authors:  S Dalton
Journal:  EMBO J       Date:  1992-05       Impact factor: 11.598

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  15 in total

1.  Mad4 is regulated by a transcriptional repressor complex that contains Miz-1 and c-Myc.

Authors:  Louise Kime; Stephanie C Wright
Journal:  Biochem J       Date:  2003-02-15       Impact factor: 3.857

2.  The transcriptional repressor gene Mad3 is a novel target for regulation by E2F1.

Authors:  Elizabeth J Fox; Stephanie C Wright
Journal:  Biochem J       Date:  2003-02-15       Impact factor: 3.857

Review 3.  Functional interactions among members of the MAX and MLX transcriptional network during oncogenesis.

Authors:  Daniel Diolaiti; Lisa McFerrin; Patrick A Carroll; Robert N Eisenman
Journal:  Biochim Biophys Acta       Date:  2014-05-22

4.  Focus formation: a cell-based assay to determine the oncogenic potential of a gene.

Authors:  Angel Alvarez; Gustavo A Barisone; Elva Diaz
Journal:  J Vis Exp       Date:  2014-12-31       Impact factor: 1.355

5.  Loss of MXD3 induces apoptosis of Reh human precursor B acute lymphoblastic leukemia cells.

Authors:  Gustavo A Barisone; Noriko Satake; Carly Lewis; Connie Duong; Cathy Chen; Kit S Lam; Jan Nolta; Elva Dίaz
Journal:  Blood Cells Mol Dis       Date:  2014-12-20       Impact factor: 3.039

Review 6.  Normal and Neoplastic Growth Suppression by the Extended Myc Network.

Authors:  Edward V Prochownik; Huabo Wang
Journal:  Cells       Date:  2022-02-21       Impact factor: 6.600

7.  A novel role of the Mad family member Mad3 in cerebellar granule neuron precursor proliferation.

Authors:  Jun-Soo Yun; Jennifer M Rust; Tatsuto Ishimaru; Elva Díaz
Journal:  Mol Cell Biol       Date:  2007-09-24       Impact factor: 4.272

8.  Binding of human papillomavirus type 16 E6 to E6AP is not required for activation of hTERT.

Authors:  Pedja Sekaric; Jonathan J Cherry; Elliot J Androphy
Journal:  J Virol       Date:  2007-10-17       Impact factor: 5.103

9.  PRELI (protein of relevant evolutionary and lymphoid interest) is located within an evolutionarily conserved gene cluster on chromosome 5q34-q35 and encodes a novel mitochondrial protein.

Authors:  Elizabeth J Fox; Sally A Stubbs; Jimmy Kyaw Tun; Jack P Leek; Alexander F Markham; Stephanie C Wright
Journal:  Biochem J       Date:  2004-03-15       Impact factor: 3.857

10.  Role of MXD3 in proliferation of DAOY human medulloblastoma cells.

Authors:  Gustavo A Barisone; Tin Ngo; Martin Tran; Daniel Cortes; Mehdi H Shahi; Tuong-Vi Nguyen; Daniel Perez-Lanza; Wanna Matayasuwan; Elva Díaz
Journal:  PLoS One       Date:  2012-07-10       Impact factor: 3.240

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