Abstract
Recent studies of beta-globin gene expression have concentrated on the analysis of factor binding and chromatin structure within the endogenous locus. These studies have more precisely defined the extent and nature of the active chromosomal domain and the elements that organize it. Surprisingly, the beta-globin locus control region (LCR), although critical for high-level gene expression, plays little role in the overall architecture of the active locus. Analysis of the effects of targeted deletion of the beta-globin LCR, along with emerging knowledge of the behavior of the erythroid transcription factor NF-E2, leads to a new perspective on factor binding and LCR function.
Publication types
-
Research Support, Non-U.S. Gov't
-
Review
MeSH terms
-
Acetylation
-
Acetyltransferases / genetics
-
Acetyltransferases / metabolism
-
Animals
-
Chromatin / genetics*
-
Chromatin / metabolism
-
DNA-Binding Proteins / genetics
-
DNA-Binding Proteins / metabolism
-
Erythroid-Specific DNA-Binding Factors
-
Gene Expression Regulation
-
Globins / genetics*
-
Globins / metabolism
-
Histone Acetyltransferases
-
Histones / genetics
-
Histones / metabolism
-
Humans
-
Locus Control Region / genetics
-
MafK Transcription Factor
-
NF-E2 Transcription Factor
-
NF-E2 Transcription Factor, p45 Subunit
-
Nuclear Proteins / genetics
-
Nuclear Proteins / metabolism
-
Promoter Regions, Genetic / genetics
-
Protein Binding
-
Saccharomyces cerevisiae Proteins*
-
Transcription Factors / genetics
-
Transcription Factors / metabolism
Substances
-
Chromatin
-
DNA-Binding Proteins
-
Erythroid-Specific DNA-Binding Factors
-
Histones
-
MAFK protein, human
-
MafK Transcription Factor
-
NF-E2 Transcription Factor
-
NF-E2 Transcription Factor, p45 Subunit
-
NFE2 protein, human
-
Nuclear Proteins
-
Saccharomyces cerevisiae Proteins
-
Transcription Factors
-
Globins
-
Acetyltransferases
-
Histone Acetyltransferases