The DQ subregion of the human major histocomparibility complex (HLA) contains two pairs of loci: the DQA1/B1 genes (hereafter called DQ1), coding for thr DQ molecules, and the DQA2/B2 pseudogenes (hereafter called DQ2). These pseudogenes are highly homologous to the functional DQ1 genes and they have no apparent abnormal features in their sequences that could prevent their activity. Only recently a low expression of the DQA2 gene has been observed whereas the DQB2 transcript was never found. The comparison between the DQ1 and DQ2 regulatory sequences revealed several differences in their W, X, and Y cis-acting elements. To examine the DNA/protein interactions in the DQ promoter regions, we performed in vivo footprinting experiments. Whereas the functional DQ1 loci showed a series of DNA-protein contact points in the X and Y boxes, the promoters of the DQ2 pseudogenes displayed an unoccupied phenotype. These findings suggest that the very low level of DQA2 expression and the apparent lack of DQB2 activity are caused by the reduced binding affinity of specific transcription factors. (C) American Society fur Histocompatibility and Immunogenetics, 2001. Published by Elsevier Science Inc.
Absence of in vivo DNA-protein interactions in the DQA2 and DQB2 promoter regions / Paola, Indovina; Megiorni, Francesca; Giulia, Fontemaggi; Pietro, Coni; Barbara, Mora; Mazzilli, Maria Cristina. - In: HUMAN IMMUNOLOGY. - ISSN 0198-8859. - STAMPA. - 62:5(2001), pp. 504-508. [10.1016/s0198-8859(01)00236-1]
Absence of in vivo DNA-protein interactions in the DQA2 and DQB2 promoter regions
MEGIORNI, Francesca;MAZZILLI, Maria Cristina
2001
Abstract
The DQ subregion of the human major histocomparibility complex (HLA) contains two pairs of loci: the DQA1/B1 genes (hereafter called DQ1), coding for thr DQ molecules, and the DQA2/B2 pseudogenes (hereafter called DQ2). These pseudogenes are highly homologous to the functional DQ1 genes and they have no apparent abnormal features in their sequences that could prevent their activity. Only recently a low expression of the DQA2 gene has been observed whereas the DQB2 transcript was never found. The comparison between the DQ1 and DQ2 regulatory sequences revealed several differences in their W, X, and Y cis-acting elements. To examine the DNA/protein interactions in the DQ promoter regions, we performed in vivo footprinting experiments. Whereas the functional DQ1 loci showed a series of DNA-protein contact points in the X and Y boxes, the promoters of the DQ2 pseudogenes displayed an unoccupied phenotype. These findings suggest that the very low level of DQA2 expression and the apparent lack of DQB2 activity are caused by the reduced binding affinity of specific transcription factors. (C) American Society fur Histocompatibility and Immunogenetics, 2001. Published by Elsevier Science Inc.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.