Literature DB >> 17077320

Transcriptional interference among the murine beta-like globin genes.

Xiao Hu1, Susan Eszterhas, Nicolas Pallazzi, Eric E Bouhassira, Jennifer Fields, Osamu Tanabe, Scott A Gerber, Michael Bulger, James Douglas Engel, Mark Groudine, Steven Fiering.   

Abstract

Mammalian beta-globin loci contain multiple genes that are activated at different developmental stages. Studies have suggested that the transcription of one gene in a locus can influence the expression of the other locus genes. The prevalent model to explain this transcriptional interference is that all potentially active genes compete for locus control region (LCR) activity. To investigate the influence of transcription by the murine embryonic genes on transcription of the other beta-like genes, we generated mice with deletions of the promoter regions of Ey and betah1 and measured transcription of the remaining genes. Deletion of the Ey and betah1 promoters increased transcription of betamajor and betaminor 2-fold to 3-fold during primitive erythropoiesis. Deletion of Ey did not affect betah1 nor did deletion of betah1 affect Ey, but Ey deletion uniquely activated transcription from betah0, a beta-like globin gene immediately downstream of Ey. Protein analysis showed that betah0 encodes a translatable beta-like globin protein that can pair with alpha globin. The lack of transcriptional interference between Ey and betah1 and the gene-specific repression of betah0 did not support LCR competition among the embryonic genes and suggested that direct transcriptional interference from Ey suppressed betah0.

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Year:  2006        PMID: 17077320      PMCID: PMC1801066          DOI: 10.1182/blood-2006-06-029868

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  31 in total

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Authors:  Xiao Hu; Michael Bulger; Julia N Roach; Susan K Eszterhas; Emmanuel Olivier; Eric E Bouhassira; Mark T Groudine; Steven Fiering
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  16 in total

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7.  All of the human beta-type globin genes compete for LCR enhancer activity in embryonic erythroid cells of yeast artificial chromosome transgenic mice.

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