The role of BTB domain-containing zinc finger proteins in T cell development and function

被引:48
作者
Bilic, Ivan [1 ]
Ellmeier, Wilfried [1 ]
机构
[1] Med Univ Vienna, Inst Immunol, A-1090 Vienna, Austria
基金
奥地利科学基金会;
关键词
T cell development; T cell subsets; BTB domain; zinc finger; gene expression; transcriptional regulation; gene knockout;
D O I
10.1016/j.imlet.2006.09.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cell fate specifications during T lymphocyte differentiation result from the orchestrated expression of developmentally regulated genes. Furthermore, epigenetic processes that result in a heritable chromatin structure are required for the maintenance of gene expression programs within cells. More and more is known about the basic mechanisms of T cell development and their diversification into various peripheral T cell subsets. Recent research has begun to provide insight into the interactive network of transcription factors as critical regulators of T lymphocyte differentiation. In the past years several members of the BTB domain-containing family of zinc finger proteins (BTB-ZF) have been described to be important for the development and function of hematopoietic cells, and also to contribute to malignant hematopoiesis. This review will provide a brief overview about the role of BTB-ZF proteins during thymocyte development and T cell function. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 87 条
[41]   A combinatorial code for gene expression generated by transcription factor Bach2 and MAZR (MAZ-related factor) through the BTB/POZ domain [J].
Kobayashi, A ;
Yamagiwa, H ;
Hoshino, H ;
Muto, A ;
Sato, K ;
Morita, M ;
Hayashi, N ;
Yamamoto, M ;
Igarashi, K .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (05) :1733-1746
[42]   Transcriptional repressor BCL-6 immortalizes germinal center-like B cells in the absence of p53 function [J].
Kusam, S ;
Vasanwala, FH ;
Dent, AL .
ONCOGENE, 2004, 23 (03) :839-844
[43]   Understanding the generation and function of memory T cell subsets [J].
Lanzavecchia, A ;
Sallusto, F .
CURRENT OPINION IN IMMUNOLOGY, 2005, 17 (03) :326-332
[44]   NFAT proteins: Key regulators of T-cell development and function [J].
Macian, F .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (06) :472-484
[45]   BCL6b mediates the enhanced magnitude of the secondary response of memory CD8+ T lymphocytes [J].
Manders, PM ;
Hunter, PJ ;
Telaranta, AI ;
Carr, JM ;
Marshall, JL ;
Carrasco, M ;
Murakami, Y ;
Palmowski, MJ ;
Cerundolo, V ;
Kaech, SM ;
Ahmed, R ;
Fearon, DT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (21) :7418-7425
[46]   In-depth mutational analysis of the promyelocytic leukemia zinc finger BTB/POZ domain reveals motifs and residues required for biological and transcriptional functions [J].
Melnick, A ;
Ahmad, KF ;
Arai, S ;
Polinger, A ;
Ball, H ;
Borden, KL ;
Carlile, GW ;
Prive, GG ;
Licht, JD .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (17) :6550-6567
[47]   Critical residues within the BTB domain of PLZF and bcl-6 modulate interaction with corepressors [J].
Melnick, A ;
Carlile, G ;
Ahmad, KF ;
Kiang, CL ;
Corcoran, C ;
Bardwell, V ;
Prive, GG ;
Licht, JD .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (06) :1804-1818
[48]   A repressor of GATA-mediated negative feedback mechanism of T cell activation [J].
Miaw, SC ;
Kang, BY ;
White, IA ;
Ho, IC .
JOURNAL OF IMMUNOLOGY, 2004, 172 (01) :170-177
[49]   ROG, repressor of GATA, regulates the expression of cytokine genes [J].
Miaw, SC ;
Choi, A ;
Yu, E ;
Kishikawa, H ;
Ho, IC .
IMMUNITY, 2000, 12 (03) :323-333
[50]   Committed to memory: lineage choices for activated T cells [J].
Moulton, Vaishali R. ;
Farber, Donna L. .
TRENDS IN IMMUNOLOGY, 2006, 27 (06) :261-267