Literature DB >> 8649813

Mader: a novel nuclear protein over expressed in human melanomas.

K H Kirsch1, Y Korradi, J P Johnson.   

Abstract

Mader is a novel delayed early response gene encoding a nuclear protein. Upregulation of the Mader 2.7 kb mRNA requires protein synthesis and can be induced in a variety of human cell lines by serum stimulation and in freshly isolated lymphocytes by mitogens. mRNA levels reach a maximum by 2 h and return to basal levels by 6 h. Mader is highly conserved as cross-hybridizing DNA sequences were observed in species as diverse as Rhesus and S. cerevisiae. The Mader protein of approximately 55 kD has two proline rich domains and contains 15 potential phosphorylation sites, a nuclear localization signal, and multiple S(T)PXX motifs that are characteristic of regulatory DNA binding proteins. Monoclonal antibodies produced against Mader confirm that it is localized to the nucleus. These features of Mader suggest that it may play a role in growth regulation. Although Mader mRNA can be detected in most cell lines, only occasional immunoreactive cells were detected in normal human tissues. In contrast, uniform strong nuclear staining was observed in all malignant melanomas examined. The fact that only one of six benign melanocytic nevi examined showed evidence of Mader expression suggests that over-expression of Mader protein may be associated with the malignant transformation of melanocytes.

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Year:  1996        PMID: 8649813

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  10 in total

1.  EGR1, EGR2, and EGR3 activate the expression of their coregulator NAB2 establishing a negative feedback loop in cells of neuroectodermal and epithelial origin.

Authors:  Joerg Kumbrink; Kathrin H Kirsch; Judith P Johnson
Journal:  J Cell Biochem       Date:  2010-09-01       Impact factor: 4.429

2.  Regulation of p130(Cas)/BCAR1 expression in tamoxifen-sensitive and tamoxifen-resistant breast cancer cells by EGR1 and NAB2.

Authors:  Joerg Kumbrink; Kathrin H Kirsch
Journal:  Neoplasia       Date:  2012-02       Impact factor: 5.715

3.  Nab1, a corepressor of NGFI-A (Egr-1), contains an active transcriptional repression domain.

Authors:  A H Swirnoff; E D Apel; J Svaren; B R Sevetson; D B Zimonjic; N C Popescu; J Milbrandt
Journal:  Mol Cell Biol       Date:  1998-01       Impact factor: 4.272

4.  Opposing regulation of T cell function by Egr-1/NAB2 and Egr-2/Egr-3.

Authors:  Sam Collins; Michael A Lutz; Paul E Zarek; Robert A Anders; Gilbert J Kersh; Jonathan D Powell
Journal:  Eur J Immunol       Date:  2008-02       Impact factor: 5.532

5.  p130Cas acts as survival factor during PMA-induced apoptosis in HL-60 promyelocytic leukemia cells.

Authors:  Joerg Kumbrink; Kathrin H Kirsch
Journal:  Int J Biochem Cell Biol       Date:  2012-12-31       Impact factor: 5.085

6.  Novel mutants of NAB corepressors enhance activation by Egr transactivators.

Authors:  J Svaren; B R Sevetson; T Golda; J J Stanton; A H Swirnoff; J Milbrandt
Journal:  EMBO J       Date:  1998-10-15       Impact factor: 11.598

7.  Epidermal growth factor receptor (EGFR) signaling promotes proliferation and survival in osteoprogenitors by increasing early growth response 2 (EGR2) expression.

Authors:  Abhishek Chandra; Shenghui Lan; Ji Zhu; Valerie A Siclari; Ling Qin
Journal:  J Biol Chem       Date:  2013-05-29       Impact factor: 5.157

8.  Discovering biomarkers from gene expression data for predicting cancer subgroups using neural networks and relational fuzzy clustering.

Authors:  Nikhil R Pal; Kripamoy Aguan; Animesh Sharma; Shun-ichi Amari
Journal:  BMC Bioinformatics       Date:  2007-01-06       Impact factor: 3.169

9.  Differential regulation of NAB corepressor genes in Schwann cells.

Authors:  Rajini Srinivasan; Sung-Wook Jang; Rebecca M Ward; Shrikesh Sachdev; Toshihiko Ezashi; John Svaren
Journal:  BMC Mol Biol       Date:  2007-12-20       Impact factor: 2.946

10.  The transcriptional corepressor NAB2 inhibits NGF-induced differentiation of PC12 cells.

Authors:  Z Qu; L A Wolfraim; J Svaren; M U Ehrengruber; N Davidson; J Milbrandt
Journal:  J Cell Biol       Date:  1998-08-24       Impact factor: 10.539

  10 in total

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