Regulation of CD40 and CD40 ligand by the AT-hook transcription factor AKNA

被引:76
作者
Siddiqa, A
Sims-Mourtada, JC
Guzman-Rojas, L
Rangel, R
Guret, C
Madrid-Marina, V
Sun, Y
Martinez-Valdez, H
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
[2] Schering Plough, Lab Immunol Res, F-69571 Dardilly, France
[3] Inst Nacl Salud Publ, Ctr Invest Sobre Enfermedades Infecciosas, Cuernavaca 62508, Morelos, Mexico
关键词
D O I
10.1038/35066602
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Proteins containing AT hooks bind A/T-rich DNA through a nine-amino-acid motif and are thought to co-regulate transcription by modifying the architecture of DNA, thereby enhancing the accessibility of promoters to transcription factors(1,2). Here we describe AKNA, a human AT-hook protein that directly binds the A/T-rich regulatory elements of the promoters of CD40 and CD40 ligand (CD40L) and coordinately regulates their expression. Consistent with its function, AKNA is a nuclear protein that contains multiple PEST protein-cleavage motifs, which are common in regulatory proteins with high turnover rates(3). AKNA is mainly expressed by B and T lymphocytes, natural killer cells and dendritic cells. During B-lymphocyte differentiation, AKNA is mainly expressed by germinal centre B lymphocytes, a stage in which receptor and ligand interactions are crucial for B-lymphocyte maturation(4-12). Our findings show that an AT-hook molecule can coordinately regulate the expression of a key receptor and its ligand, and point towards a molecular mechanism that explains homotypic cell interactions.
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页码:383 / 387
页数:6
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