Repression of transcription at the human T-cell receptor Vβ2.2 segment is mediated by a MAX/MAD/mSin3 complex acting as a scaffold for HDAC activity

Biochemical and Biophysical Research Communications

Volumn 325, Issue 3, 2004, Pages 1021-1029

  Font, Marie Pierre ^a   Cubizolles, Myriam ^b   Dombret, Hervé ^a   Cazes, Lucien ^c   Brenac, Virginie ^b   Sigaux, François ^a   Buckle, Malcolm ^d  

^a SAINT LOUIS HOSPITAL   (France)

^b CIPHERGEN BIOSYSTEMS INC   (United States)

^c 27 Place Julliette Dodu   (France)

^d Ecole Normale Superieure de Cachan   (France)

Author keywords

LC MS; MAX MAD regulatory networks; ProteinChip; SELDI; SPR; T cell receptor; Transcription

Indexed keywords

HISTONE DEACETYLASE; MAD PROTEIN; MAX PROTEIN; MSIN3 PROTEIN; PROTEIN; T LYMPHOCYTE RECEPTOR; UNCLASSIFIED DRUG;

ARTICLE; COMPLEX FORMATION; CONTROLLED STUDY; DESORPTION; ELECTROSPRAY MASS SPECTROMETRY; ENZYME ACTIVITY; ENZYME INHIBITION; HUMAN; HUMAN CELL; LASER; LEUKEMIA CELL LINE; MASS SPECTROMETRY; PRIORITY JOURNAL; SILENCER GENE; SURFACE PLASMON RESONANCE;

DNA-BINDING PROTEINS; DOWN-REGULATION; GENE EXPRESSION REGULATION; HISTONE DEACETYLASES; HUMANS; JURKAT CELLS; PROMOTER REGIONS (GENETICS); RECEPTORS, ANTIGEN, T-CELL, ALPHA-BETA; REPRESSOR PROTEINS; TRANSCRIPTION, GENETIC;

EID: 8444246695     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbrc.2004.10.139     Document Type: Article

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