Modular usage of the HLA-DRA promoter in extra-hematopoietic and hematopoietic cell types of transgenic mice

被引:3
|
作者
Giorda, E
Sibilio, L
Martayan, A
Feriotto, G
Bianchi, N
Mischiati, C
Di Rosa, F
Pozzi, L
Gambari, R
Giacomini, P
机构
[1] Regina Elena Inst Canc Res, Immunol Lab, CRS, I-00158 Rome, Italy
[2] Univ Ferrara, Ctr Biotechnol, I-44100 Ferrara, Italy
[3] Univ Ferrara, Dept Biochem & Mol Biol, Mol Biol Sect, I-44100 Ferrara, Italy
[4] Inst Genet & Biophys A Buzzati Traverso, CNR, Naples, Italy
[5] Regina Elena Inst Canc Res, Telethon Transgen Mouse Facil, CRS, I-00158 Rome, Italy
[6] Univ Ferrara, Interdisciplinary Ctr Study Inflammat, I-44100 Ferrara, Italy
关键词
class II MHC; gene regulation; IFN-gamma; transgenics;
D O I
10.1111/j.1742-4658.2005.04740.x
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
Class II MHC genes (for example, the human HLA-DRA gene) are expressed at the cell surface in many professional and nonprofessional antigen-presenting cells in a variety of anatomical locations. Here, we report about 13 mouse transgenic lines (11 of which have not been previously described) generated with four distinct sets of DRA transgenes carrying progressive, informative 5' and 3' deletions. DRA expression was assessed in B lymphocytes, dendritic cells, macrophages, and extra-hematopoietic cells (particularly kidney epithelial cells). A compact transcriptional unit was identified that efficiently directs DRA expression [both constitutive and interferon (IFN)-gamma induced] in extra-hematopoietic tissues and dendritic cells. It extends from position -266 upstream of the transcription initiation site to position + 119 downstream of the last DRA exon. The same fragment, however, did not efficiently direct IFN-gamma-induced DRA expression in macrophages, that required additional 5' sequences. Thus, IFN-gamma uses distinct promoter segments and mechanisms to up-regulate class II in different cell lineages. In contrast to previous results in transgenic mice expressing murine class II transgenes, we were unable to generate reproducible patterns of HLA-DRA expression in B cells.
引用
收藏
页码:3214 / 3226
页数:13
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共 47 条
  • [1] METHYLATION STATE OF THE HUMAN HLA-DRA GENE IN TRANSGENIC MICE
    FERIOTTO, G
    POZZI, L
    DELEDDA, F
    BARBIERI, R
    PIVA, R
    NASTRUZZI, C
    CIUCCI, A
    NATALI, PG
    GIACOMINI, P
    GAMBARI, R
    CYTOTECHNOLOGY, 1991, 5 : 55 - 56
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    CIUCCI, A
    NICOTRA, MR
    NASTRUZZI, C
    FERIOTTO, G
    APPELLA, E
    GAMBARI, R
    POZZI, L
    NATALI, PG
    IMMUNOGENETICS, 1991, 34 (06) : 385 - 391
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    ESAKI, Y
    KIMURA, A
    HIROKAWA, K
    NISHIMURA, Y
    SASAZUKI, T
    IMMUNOGENETICS, 1993, 37 (03) : 204 - 211
  • [6] MOUSE MAMMARY-TUMOR VIRUS-MEDIATED T-CELL RECEPTOR-NEGATIVE SELECTION IN HLA-DRA TRANSGENIC MICE
    ALTMANN, DM
    TAKACS, K
    TROWSDALE, J
    ELLIOTT, JI
    HUMAN IMMUNOLOGY, 1993, 37 (03) : 149 - 156
  • [7] ACTIVATION OF THE HLA-DRA GENE IN PRIMARY HUMAN LYMPHOCYTES-T - NOVEL USAGE OF TATA AND THE X-PROMOTER AND Y-PROMOTER ELEMENTS
    MATSUSHIMA, GK
    ITOHLINDSTROM, Y
    TING, JPY
    MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (12) : 5610 - 5619
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    COGSWELL, JP
    AUSTIN, J
    TING, JPY
    JOURNAL OF IMMUNOLOGY, 1991, 146 (04): : 1361 - 1367
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    Deng, H
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    Jin, TR
    Cheung, J
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