![]()
|
|
||||||||
J. Biol. Chem., Vol. 276, Issue 45, 41817-41824, November 9, 2001
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
From the Department of Human Genetics, Medical College of Virginia
Campus, Virginia Commonwealth University,
Richmond, Virginia 23298-0033
The competition model of globin gene regulation
states that the
The Human
-Globin TATA and CACCC Elements Have Key, Distinct
Roles in Suppressing
-Globin Gene Expression in Embryonic/Fetal
Development*
-globin gene precludes expression of the
-globin
gene in early development by competing for the enhancing activity of
the locus control region. The
-globin gene with a
161 promoter is sufficient for suppressing
-globin gene expression, and the
-globin TATA and CACCC elements are necessary for this effect. In
this work, stable transfection and transgenic mouse assays have been performed with constructs containing HS3 and HS2 from the locus control
region, the
-globin gene with promoter mutation(s), and the
-globin gene. The data indicate that the
-globin TATA and CACCC
elements together have at least an additive effect on the
/
-globin mRNA ratio in early erythroid cells, suggesting that the elements work coordinately to suppress
-globin gene expression. The TATA and CACCC are the major
-globin promoter elements
responsible for this effect. Transgenic mouse experiments indicate that
the
-globin TATA element plays a role in
-globin expression and
-globin suppression in the embryo and fetus; in contrast, the CACCC
element has a stage-specific effect in the fetus. The results suggest
that, as is true for the erythroid Krüppel-like factor (EKLF) and the
-globin promoter CACCC, a protein(s) binds to the
-globin CACCC element to coordinate stage-specific gene expression.
*
This work was supported by National Institutes of Health
Grant HL 60080 (to J. A. L.).The costs of publication of this
article were defrayed in part by the
payment of page charges. The article must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
To whom correspondence should be addressed: Dept. of Human
Genetics, Medical College of Virginia Campus, Virginia Commonwealth University, P. O. Box 980033, Richmond, VA 23298-0033. Tel.:
804-828-9632 (ext. 136); Fax: 804-828-3760; E-mail:
jlloyd@hsc.vcu.edu.
This article has been cited by other articles:
![]() |
Q. Li, X. Fang, I. Olave, H. Han, M. Yu, P. Xiang, and G. Stamatoyannopoulos Transcriptional potential of the {gamma}-globin gene is dependent on the CACCC box in a developmental stage-specific manner Nucleic Acids Res., September 1, 2006; 34(14): 3909 - 3916. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Yu, H. Han, P. Xiang, Q. Li, and G. Stamatoyannopoulos Autonomous Silencing as Well as Competition Controls {gamma}-Globin Gene Expression during Development. Mol. Cell. Biol., July 1, 2006; 26(13): 4775 - 4781. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Zhou, K. M. Pawlik, J. Ren, C.-W. Sun, and T. M. Townes Differential Binding of Erythroid Krupple-like Factor to Embryonic/Fetal Globin Gene Promoters during Development J. Biol. Chem., June 9, 2006; 281(23): 16052 - 16057. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y.-Q. Feng, R. Warin, T. Li, E. Olivier, A. Besse, A. Lobell, H. Fu, C. M. Lin, M. I. Aladjem, and E. E. Bouhassira The Human {beta}-Globin Locus Control Region Can Silence as Well as Activate Gene Expression Mol. Cell. Biol., May 15, 2005; 25(10): 3864 - 3874. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Hu, M. Bulger, J. N. Roach, S. K. Eszterhas, E. Olivier, E. E. Bouhassira, M. T. Groudine, and S. Fiering Promoters of the murine embryonic beta -like globin genes Ey and beta h1 do not compete for interaction with the beta -globin locus control region PNAS, February 4, 2003; 100(3): 1111 - 1115. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| All ASBMB Journals | Molecular and Cellular Proteomics |
| Journal of Lipid Research | ASBMB Today |