Different requirements for signal transducer and activator of transcription 1α and interferon regulatory factor 1 in the regulation of low molecular mass polypeptide 2 and transporter associated with antigen processing 1 gene expression

被引:91
作者
Chatterjee-Kishore, M
Kishore, R
Hicklin, DJ
Marincola, FM
Ferrone, S [1 ]
机构
[1] New York Med Coll, Dept Microbiol & Immunol, Valhalla, NY 10595 USA
[2] NCI, Surg Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1074/jbc.273.26.16177
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The components of the antigen processing machinery, low molecular mass polypeptide (LMP) 2 and transporter associated with antigen processing (TAP) 1, are encoded by closely linked genes within the major histocompatibility complex class II subregion. Although the two genes share a bi-directional promoter, LMP2 and TAP1 have differential cellular expression. TAP1 is expressed constitutively. However, LMP2 expression requires induction by interferon-gamma in most cells. The regulatory elements within the LMP2/TAP1 promoter and the transcription factors that bind these elements have been defined, However, how these transactivators regulate differential TAP1 and LMP2 gene transcription is not known. We have addressed this question by analyzing three human melanoma cell lines with distinct phenotypes of LMP2 and TAP1 expression.Whereas binding of either interferon regulatory factor 1 or Stat1 to the overlapping interferon consensus sequence-2/GAS is sufficient for regulating transcription of the TAP1 gene, binding of both factors is required for LMP2 gene transcription. This conclusion is supported by restoration of LMP2 gene transcription following transfection of wild type Stat1 alpha or interferon regulatory factor 1 cDNA into cells lacking these transcription factors. The flexibility in the regulation of the TAP1 gene may reflect its role in maintaining immune surveillance. Furthermore, lack of LMP2 gene transcription in quiescent human cells suggests that LMP2 expression reflects a state of cell activation.
引用
收藏
页码:16177 / 16183
页数:7
相关论文
共 35 条
[1]   INTERFERON-GAMMA STIMULATION MODULATES THE PROTEOLYTIC ACTIVITY AND CLEAVAGE SITE PREFERENCE OF 20S MOUSE PROTEASOMES [J].
BOES, B ;
HENGEL, H ;
RUPPERT, T ;
MULTHAUP, G ;
KOSZINOWSKI, UH ;
KLOETZEL, PM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (03) :901-909
[2]   HOMOZYGOUS HUMAN TAP PEPTIDE TRANSPORTER MUTATION IN HLA CLASS-I DEFICIENCY [J].
DELASALLE, H ;
HANAU, D ;
FRICKER, D ;
URLACHER, A ;
KELLY, A ;
SALAMERO, J ;
POWIS, SH ;
DONATO, L ;
BAUSINGER, H ;
LAFORET, M ;
JERAS, M ;
SPEHNER, D ;
BIEBER, T ;
FALKENRODT, A ;
CAZENAVE, JP ;
TROWSDALE, J ;
TONGIO, MM .
SCIENCE, 1994, 265 (5169) :237-241
[3]   ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[4]   MHC-LINKED LMP GENE-PRODUCTS SPECIFICALLY ALTER PEPTIDASE ACTIVITIES OF THE PROTEASOME [J].
DRISCOLL, J ;
BROWN, MG ;
FINLEY, D ;
MONACO, JJ .
NATURE, 1993, 365 (6443) :262-264
[5]  
ELHODIRI HM, 1995, MOL CELL BIOL, V15, P3587
[6]   Transporter associated with antigen processing [J].
Elliott, T .
ADVANCES IN IMMUNOLOGY, VOL 65, 1997, 65 :47-109
[7]   PEPTIDASE ACTIVITIES OF PROTEASOMES ARE DIFFERENTIALLY REGULATED BY THE MAJOR HISTOCOMPATIBILITY COMPLEX-ENCODED GENES FOR LMP2 AND LMP7 [J].
GACZYNSKA, M ;
ROCK, KL ;
SPIES, T ;
GOLDBERG, AL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (20) :9213-9217
[8]  
GouilleuxGruart V, 1996, BLOOD, V87, P1692
[9]   Immunoproteasome assembly:: Cooperative incorporation of interferon γ (IFN-γ)-inducible subunits [J].
Griffin, TA ;
Nandi, D ;
Cruz, M ;
Fehling, HJ ;
Van Kaer, L ;
Monaco, JJ ;
Colbert, RA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (01) :97-104
[10]   THE INTERFERON-GAMMA-INDUCIBLE 11S-REGULATOR (PA28) AND THE LMP2/LMP7 SUBUNITS GOVERN THE PEPTIDE PRODUCTION BY THE 20S-PROTEASOME IN-VITRO [J].
GROETTRUP, M ;
RUPPERT, T ;
KUEHN, L ;
SEEGER, M ;
STANDERA, S ;
KOSZINOWSKI, U ;
KLOETZEL, PM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (40) :23808-23815