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PMID: 7781911 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Autonomous, erythroid-specific DNase I hypersensitive site formed by human beta-globin locus control region (LCR) 5' HS 2 in transgenic mice.

Developmental biology ·Vol. 169 ·No. 2 ·1995-06-00 ·Pages 728-32

Pawlik KM, Townes TM

Abstract

The human beta-globin locus control region (LCR) is composed of four erythroid-specific, DNase I hypersensitive (HS) sites that are located 6 to 18 kb upstream of the epsilon-globin gene. The beta-globin LCR appears to have two major functions. First, the sequences "open" a chromosomal domain that includes the epsilon-, gamma-, and beta-globin genes and, second, the LCR directs high-level, erythroid-specific expression of each globin gene family member. An LCR subfragment containing only 5' HS 2 can confer these properties on a linked beta-globin gene. To determine whether 5' HS 2 can form an erythroid-specific, DNase I hypersensitive site in the absence of a linked globin gene, a 1.9-kb DNA fragment containing this site was injected into fertilized mouse eggs and DNase I hypersensitivity was analyzed in the animals that developed. In 9 of 10 transgenic mouse lines, the human 5' HS 2 fragment formed a DNase I hypersensitive site in fetal liver but not in fetal brain. These results suggest that human 5' HS 2 can function autonomously to organize an open chromatin domain specifically in erythroid cells.

MeSH Terms
Animals Brain/embryology,metabolism Chromosomes, Human, Pair 11 Deoxyribonuclease I/metabolism Erythrocytes/metabolism Globins/genetics Humans Liver/embryology,metabolism Mice Mice, Transgenic
Chemicals
Globins Deoxyribonuclease I
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Pawlik K M
Department of Biochemistry and Molecular Genetics, School of Medicine, University of Alabama at Birmingham 35294, USA.
Townes T M
Article Info
Journal
Developmental biology
Abbr.
Dev Biol
ISSN
0012-1606
Published
1995-06-00
Pages
728-32
Language
English
Region
United States
NLM ID
0372762
Subset
IM
Grants
NHLBI NIH HHS · HL 35559 · United States
NHLBI NIH HHS · HL 43508 · United States
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