Mutations in the gene autoimmune regulator (AIRE) cause autoimmune polyendocrinopathy candidiasis ectodermal dystrophy. AIRE is expressed in thymic medullary epithelial cells, where it promotes the expression of tissue-restricted antigens. By the combined use of biochemical and biophysical methods, we show that AIRE selectively interacts with histone H3 through its first plant homeodomain (PHD) finger (AIRE-PHD1) and preferentially binds to non-methylated H3K4 (H3K4me0). Accordingly, in vivo AIRE binds to and activates promoters containing low levels of H3K4me3 in human embryonic kidney 293 cells. We conclude that AIRE-PHD1 is an important member of a newly identified class of PHD fingers that specifically recognize H3K4me0, thus providing a new link between the status of histone modifications and the regulation of tissue-restricted antigen expression in thymus.

The autoimmune regulator PHD finger binds to non-methylated histone H3K4 to activate gene expression / T. Org, F. Chignola, C. Hetényi, M. Gaetani, A. Rebane, I. Liiv, U. Maran, L. Mollica, M.J. Bottomley, G. Musco, P. Peterson. - In: EMBO REPORTS. - ISSN 1469-221X. - 9:4(2008 Apr), pp. 370-376.

The autoimmune regulator PHD finger binds to non-methylated histone H3K4 to activate gene expression

F. Chignola
Secondo
;
L. Mollica;
2008

Abstract

Mutations in the gene autoimmune regulator (AIRE) cause autoimmune polyendocrinopathy candidiasis ectodermal dystrophy. AIRE is expressed in thymic medullary epithelial cells, where it promotes the expression of tissue-restricted antigens. By the combined use of biochemical and biophysical methods, we show that AIRE selectively interacts with histone H3 through its first plant homeodomain (PHD) finger (AIRE-PHD1) and preferentially binds to non-methylated H3K4 (H3K4me0). Accordingly, in vivo AIRE binds to and activates promoters containing low levels of H3K4me3 in human embryonic kidney 293 cells. We conclude that AIRE-PHD1 is an important member of a newly identified class of PHD fingers that specifically recognize H3K4me0, thus providing a new link between the status of histone modifications and the regulation of tissue-restricted antigen expression in thymus.
apr-2008
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/48895
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