Transcription factor NF-kappa B regulates inducible Oct-2 gene expression in precursor B lymphocytes

被引:29
作者
Bendall, HH
Scherer, DC
Edson, CR
Ballard, DW
Oltz, EM
机构
[1] VANDERBILT UNIV,SCH MED,DEPT MICROBIOL & IMMUNOL,NASHVILLE,TN 37232
[2] VANDERBILT UNIV,SCH MED,HOWARD HUGHES MED INST,NASHVILLE,TN 37232
关键词
D O I
10.1074/jbc.272.46.28826
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 POU transcription factors Oct-1 and Oct-2 regulate the activity of octamer-dependent promoters, including those that direct transcription from rearranged immunoglobulin genes, Unlike Oct-1, which is constitutively expressed in many cell types, Oct-2 expression is restricted primarily to B lymphocytes and can be induced in precursor B cells by stimulation with bacterial Lipopolysaccharide (LPS), However, the precise factors that mediate this induction mechanism remain unknown. In the present study, we monitored Oct-2; expression in cells arrested for the activation of NF-kappa B, an LPS-responsive member of the Rel transcription factor family. Despite stimulation with LPS, disruption of the NF-kappa B signaling pathway in precursor B cells led to the loss of inducible Oct-2 DNA binding activity in vitro and the suppression of Oct-2-directed transcription in vivo. This biochemical defect correlated with a specific block to Oct-2 gene expression at the level of transcription, whereas the expression of Oct-1 was unaffected. The finding that Oct-2 is under NF-kappa B control highlights an important cross-talk mechanism involving two distinct transcription factor families that regulate B lymphocyte function.
引用
收藏
页码:28826 / 28828
页数:3
相关论文
共 22 条
  • [1] The NF-kappa B and I kappa B proteins: New discoveries and insights
    Baldwin, AS
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 : 649 - 683
  • [2] THE V-REL ONCOGENE ENCODES A KAPPA-B ENHANCER BINDING-PROTEIN THAT INHIBITS NF-KAPPA-B FUNCTION
    BALLARD, DW
    WALKER, WH
    DOERRE, S
    SISTA, P
    MOLITOR, JA
    DIXON, EP
    PEFFER, NJ
    HANNINK, M
    GREENE, WC
    [J]. CELL, 1990, 63 (04) : 803 - 814
  • [3] BAUERLE PA, 1988, SCIENCE, V242, P540
  • [4] BROCKMAN JA, 1995, MOL CELL BIOL, V15, P2809
  • [5] AN ACTIVE V-ABL PROTEIN-TYROSINE KINASE BLOCKS IMMUNOGLOBULIN LIGHT-CHAIN GENE REARRANGEMENT
    CHEN, YY
    WANG, LC
    HUANG, MS
    ROSENBERG, N
    [J]. GENES & DEVELOPMENT, 1994, 8 (06) : 688 - 697
  • [6] OCT-2, ALTHOUGH NOT REQUIRED FOR EARLY B-CELL DEVELOPMENT, IS CRITICAL FOR LATER B-CELL MATURATION AND FOR POSTNATAL SURVIVAL
    CORCORAN, LM
    KARVELAS, M
    NOSSAL, GJV
    YE, ZS
    JACKS, T
    BALTIMORE, D
    [J]. GENES & DEVELOPMENT, 1993, 7 (04) : 570 - 582
  • [7] GSTAIGER M, 1995, NATURE, V373, P60
  • [8] THE POU DOMAIN - A LARGE CONSERVED REGION IN THE MAMMALIAN PIT-1, OCT-1, OCT-2, AND CAENORHABDITIS-ELEGANS UNC-86 GENE-PRODUCTS
    HERR, W
    STURM, RA
    CLERC, RG
    CORCORAN, LM
    BALTIMORE, D
    SHARP, PA
    INGRAHAM, HA
    ROSENFELD, MG
    FINNEY, M
    RUVKUN, G
    HORVITZ, HR
    [J]. GENES & DEVELOPMENT, 1988, 2 (12A) : 1513 - 1516
  • [9] OCTAMER TRANSCRIPTION FACTORS AND THE CELL TYPE-SPECIFICITY OF IMMUNOGLOBULIN GENE-EXPRESSION
    KEMLER, I
    SCHAFFNER, W
    [J]. FASEB JOURNAL, 1990, 4 (05) : 1444 - 1449
  • [10] IDENTIFICATION OF CD36 AS THE FIRST GENE DEPENDENT ON THE B-CELL DIFFERENTIATION FACTOR OCT-2
    KONIG, H
    PFISTERER, P
    CORCORAN, LM
    WIRTH, T
    [J]. GENES & DEVELOPMENT, 1995, 9 (13) : 1598 - 1607