Transcriptional interference among the murine β-like globin genes

Author:

Hu Xiao1,Eszterhas Susan1,Pallazzi Nicolas2,Bouhassira Eric E.2,Fields Jennifer1,Tanabe Osamu3,Gerber Scott A.4,Bulger Michael5,Engel James Douglas3,Groudine Mark6,Fiering Steven14

Affiliation:

1. Department of Microbiology/Immunology and Norris Cotton Cancer Center, Dartmouth Medical School, Hanover, NH;

2. Department of Medicine, Division of Hematology, Albert Einstein College of Medicine, Bronx, NY;

3. Department of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor;

4. Department of Genetics and Norris Cotton Cancer Center, Dartmouth Medical School, Hanover, NH;

5. Center for Human Genetics and Molecular Pediatric Disease and Department of Biophysics and Biochemistry, University of Rochester, NY;

6. Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA

Abstract

AbstractMammalian β-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 β-like genes, we generated mice with deletions of the promoter regions of Ey and βh1 and measured transcription of the remaining genes. Deletion of the Ey and βh1 promoters increased transcription of βmajor and βminor 2-fold to 3-fold during primitive erythropoiesis. Deletion of Ey did not affect βh1 nor did deletion of βh1 affect Ey, but Ey deletion uniquely activated transcription from βh0, a β-like globin gene immediately downstream of Ey. Protein analysis showed that βh0 encodes a translatable β-like globin protein that can pair with alpha globin. The lack of transcriptional interference between Ey and βh1 and the gene-specific repression of βh0 did not support LCR competition among the embryonic genes and suggested that direct transcriptional interference from Ey suppressed βh0.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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