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

被引:0
作者
Aisha Siddiqa
Jennifer C. Sims-Mourtada
Liliana Guzman-Rojas
Roberto Rangel
Christiane Guret
Vicente Madrid-Marina
Yan Sun
Hector Martinez-Valdez
机构
[1] Box 178,Department of Immunology
[2] The University of Texas M. D. Anderson Cancer Center,undefined
[3] Laboratory for Immunology Research,undefined
[4] Schering-Plough,undefined
[5] Centro de Investigacion Sobre Enfermedades Infecciosas,undefined
[6] Instituto Nacional de Salud Publica,undefined
来源
Nature | 2001年 / 410卷
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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 factors1,2. 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 rates3. 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 maturation4,5,6,7,8,9,10,11,12. 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:4
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