M R Stallcup

Summary

Affiliation: University of Southern California
Country: USA

Publications

  1. ncbi Co-operation between protein-acetylating and protein-methylating co-activators in transcriptional activation
    M R Stallcup
    Department of Pathology, University of Southern California, 2011 Zonal Avenue, Los Angeles, CA 90089, USA
    Biochem Soc Trans 28:415-8. 2000
  2. ncbi Multiple signal input and output domains of the 160-kilodalton nuclear receptor coactivator proteins
    H Ma
    Departments of Pathology, University of Southern California, Los Angeles, California 90033, USA
    Mol Cell Biol 19:6164-73. 1999
  3. ncbi Synergistic enhancement of nuclear receptor function by p160 coactivators and two coactivators with protein methyltransferase activities
    S S Koh
    Department of Pathology, University of Southern California, Los Angeles, California 90089, USA
    J Biol Chem 276:1089-98. 2001
  4. ncbi Regulation of transcription by a protein methyltransferase
    D Chen
    Department of Pathology HMR 301, University of Southern California, 2011 Zonal Avenue, Los Angeles, CA 90033, USA
    Science 284:2174-7. 1999
  5. ncbi Enhancement of p53-dependent gene activation by the transcriptional coactivator Zac1
    S M Huang
    Department of Pathology, University of Southern California, Los Angeles, California, CA 90089, USA
    Oncogene 20:2134-43. 2001
  6. ncbi Hormone-dependent, CARM1-directed, arginine-specific methylation of histone H3 on a steroid-regulated promoter
    H Ma
    Department of Pathology, HMR 301, University of Southern California, 2011 Zonal Avenue, Los Angeles, CA 90089, USA
    Curr Biol 11:1981-5. 2001
  7. ncbi Hormone-independent transcriptional activation and coactivator binding by novel orphan nuclear receptor ERR3
    H Hong
    Department of Pathology, University of Southern California, Los Angeles, California 90033, USA
    J Biol Chem 274:22618-26. 1999
  8. ncbi The role of protein kinase A pathway and cAMP responsive element-binding protein in androgen receptor-mediated transcription at the prostate-specific antigen locus
    J Kim
    Department of Molecular Microbiology and Immunology, USC Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA 90089, USA
    J Mol Endocrinol 34:107-18. 2005
  9. ncbi Interaction of the tau2 transcriptional activation domain of glucocorticoid receptor with a novel steroid receptor coactivator, Hic-5, which localizes to both focal adhesions and the nuclear matrix
    L Yang
    Department of Pathology and Department of Biochemistry and Molecular Biology, University of Southern California, Los Angeles, California 90089, USA
    Mol Biol Cell 11:2007-18. 2000
  10. ncbi Mouse Zac1, a transcriptional coactivator and repressor for nuclear receptors
    S M Huang
    Departments of Pathology and of Biochemistry and Molecular Biology, University of Southern California, Los Angeles, California 90089, USA
    Mol Cell Biol 20:1855-67. 2000

Collaborators

Detail Information

Publications17

  1. ncbi Co-operation between protein-acetylating and protein-methylating co-activators in transcriptional activation
    M R Stallcup
    Department of Pathology, University of Southern California, 2011 Zonal Avenue, Los Angeles, CA 90089, USA
    Biochem Soc Trans 28:415-8. 2000
    ..We propose that the synergy of co-activator function between p300, CARM1 and PRMT1 is due to their different but complementary protein modification activities...
  2. ncbi Multiple signal input and output domains of the 160-kilodalton nuclear receptor coactivator proteins
    H Ma
    Departments of Pathology, University of Southern California, Los Angeles, California 90033, USA
    Mol Cell Biol 19:6164-73. 1999
    ....
  3. ncbi Synergistic enhancement of nuclear receptor function by p160 coactivators and two coactivators with protein methyltransferase activities
    S S Koh
    Department of Pathology, University of Southern California, Los Angeles, California 90089, USA
    J Biol Chem 276:1089-98. 2001
    ..Because multiple coactivators are presumably required to mediate transcriptional activation of native genes in vivo, the low-NR conditions may provide a more physiologically relevant assay for coactivator function...
  4. ncbi Regulation of transcription by a protein methyltransferase
    D Chen
    Department of Pathology HMR 301, University of Southern California, 2011 Zonal Avenue, Los Angeles, CA 90033, USA
    Science 284:2174-7. 1999
    ..Thus, coactivator-mediated methylation of proteins in the transcription machinery may contribute to transcriptional regulation...
  5. ncbi Enhancement of p53-dependent gene activation by the transcriptional coactivator Zac1
    S M Huang
    Department of Pathology, University of Southern California, Los Angeles, California, CA 90089, USA
    Oncogene 20:2134-43. 2001
    ....
  6. ncbi Hormone-dependent, CARM1-directed, arginine-specific methylation of histone H3 on a steroid-regulated promoter
    H Ma
    Department of Pathology, HMR 301, University of Southern California, 2011 Zonal Avenue, Los Angeles, CA 90089, USA
    Curr Biol 11:1981-5. 2001
    ..Thus, arginine-specific histone methylation by CARM1 is an important part of the transcriptional activation process...
  7. ncbi Hormone-independent transcriptional activation and coactivator binding by novel orphan nuclear receptor ERR3
    H Hong
    Department of Pathology, University of Southern California, Los Angeles, California 90033, USA
    J Biol Chem 274:22618-26. 1999
    ..Although ERR3 is much more closely related to ERR2 than to ERR1, the expression pattern for ERR3 was similar to that of ERR1 and distinct from that for ERR2, suggesting a unique role for ERR3 in development...
  8. ncbi The role of protein kinase A pathway and cAMP responsive element-binding protein in androgen receptor-mediated transcription at the prostate-specific antigen locus
    J Kim
    Department of Molecular Microbiology and Immunology, USC Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA 90089, USA
    J Mol Endocrinol 34:107-18. 2005
    ..These results demonstrate an intriguing interplay between a signal transduction pathway, coactivator overexpression and AR signaling as a possible combined mechanism of progression to androgen-independent prostate cancer...
  9. ncbi Interaction of the tau2 transcriptional activation domain of glucocorticoid receptor with a novel steroid receptor coactivator, Hic-5, which localizes to both focal adhesions and the nuclear matrix
    L Yang
    Department of Pathology and Department of Biochemistry and Molecular Biology, University of Southern California, Los Angeles, California 90089, USA
    Mol Biol Cell 11:2007-18. 2000
    ....
  10. ncbi Mouse Zac1, a transcriptional coactivator and repressor for nuclear receptors
    S M Huang
    Departments of Pathology and of Biochemistry and Molecular Biology, University of Southern California, Los Angeles, California 90089, USA
    Mol Cell Biol 20:1855-67. 2000
    ..Thus, mZac1b can interact with nuclear receptors and their coactivators and play both positive and negative roles in regulating nuclear receptor function...
  11. ncbi Inhibition of p160-mediated coactivation with increasing androgen receptor polyglutamine length
    R A Irvine
    Department of Urology, University of Southern California Norris Cancer Center, University of Southern California, Keck School of Medicine, Los Angeles, CA 90033, USA
    Hum Mol Genet 9:267-74. 2000
    ..This molecular mechanism thus might explain, at least in part, the observed phenotypic effects of the AR CAG size polymorphism...
  12. ncbi Nuclear receptor-binding sites of coactivators glucocorticoid receptor interacting protein 1 (GRIP1) and steroid receptor coactivator 1 (SRC-1): multiple motifs with different binding specificities
    X F Ding
    Department of Pathology, University of Southern California, Los Angeles 90033, USA
    Mol Endocrinol 12:302-13. 1998
    ..In summary, GRIP1 and SRC-1 have overlapping NR-binding preferences, but specific NRs display both coactivator and NR Box preferences that may contribute to the specificity of hormonal responses...
  13. ncbi An additional region of coactivator GRIP1 required for interaction with the hormone-binding domains of a subset of nuclear receptors
    H Hong
    Department of Pathology, University of Southern California, Los Angeles, California 90033, USA
    J Biol Chem 274:3496-502. 1999
    ..SRC-1 lacks an NIDaux activity equivalent to that in GRIP1...
  14. ncbi Role of protein methylation in chromatin remodeling and transcriptional regulation
    M R Stallcup
    Department of Pathology, and Department of Biochemistry and Molecular Biology, University of Southern California, Los Angeles, CA 90089, USA
    Oncogene 20:3014-20. 2001
    ....
  15. ncbi Localization of the mouse glucocorticoid receptor-interacting protein 1 gene (Grip1) to proximal chromosome 1 by linkage analysis
    C L Welch
    Department of Medicine, University of California, Los Angeles, California 90095, USA
    Mamm Genome 8:620-1. 1997
  16. ncbi GRIP1, a transcriptional coactivator for the AF-2 transactivation domain of steroid, thyroid, retinoid, and vitamin D receptors
    H Hong
    Department of Pathology, University of Southern California, Los Angeles 90033, USA
    Mol Cell Biol 17:2735-44. 1997
    ..These results demonstrate directly that AF-1 and AF-2 domains accomplish their transactivation activities through different mechanisms: AF-2 requires GRIP1 as a coactivator, but AF-1 does not...
  17. ncbi GRIP1, a novel mouse protein that serves as a transcriptional coactivator in yeast for the hormone binding domains of steroid receptors
    H Hong
    Department of Pathology, University of Southern California, Los Angeles, 90033, USA
    Proc Natl Acad Sci U S A 93:4948-52. 1996
    ..Thus, in yeast, GRIP1 can serve as a coactivator, potentiating the transactivation functions in steroid receptor HBDs, possibly by acting as a bridge between HBDs of the receptors and the basal transcription machinery...