Literature DB >> 8246980

Developmental regulation of human gamma-globin genes in transgenic mice.

G Stamatoyannopoulos1, B Josephson, J W Zhang, Q Li.   

Abstract

We report results showing that several gamma gene promoter elements participate in the developmental control of gamma-globin genes. Four gamma gene constructs with 5' truncated at -141, -201, -382, and -730 of the A gamma gene promoter linked to a micro locus control region (microLCR) cassette were used for production of transgenic mice and analysis of gamma gene expression during development. Mice carrying a microLCR -141 A gamma construct displayed downregulation of gamma gene expression in the adult stage of development, indicating that the proximal promoter contains elements participating in gamma gene silencing. Mice carrying a microLCR -201 A gamma or a microLCR -382 A gamma construct displayed high gamma gene expression in the fetal stage of development and complete loss of gamma gene downregulation in the adult stage, suggesting that the -141 to -201 gamma gene sequence contains elements which upregulate gamma gene expression and are dominant over the negative element 3' to -141. Extension of the promoter to -730 resulted in reappearance of gamma gene downregulation, suggesting that the -382 to -730 sequences contain an adult-stage-specific silencer. gamma gene expression in the microLCR -201 A gamma and the microLCR -382 A gamma transgenic mice was copy number dependent. All the microLCR -730 A gamma transgenic mice expressed gamma mRNA; however, gamma gene expression was copy number independent, indicating that levels of gamma gene expression were modulated by the surrounding chromatin. Our results suggest that multiple elements participate in gamma gene silencing. The findings in the microLCR-201 A gamma and microLCR -382 A gamma transgenic mice are interpreted to indicate that the LCR interacts not only with the minimal gamma gene promoter but also with sequences of the upstream promoter. We postulate that gamma gene downregulation is achieved when the interaction between LCR and the upstream promoter is disturbed by the silencer located in the -382 to -730 region. We propose that gamma gene silencing is achieved by the combined effect of negative elements located 3' to -141, the negative element located between -382 and -730, and the competition by the beta gene promoter during the adult stage of development.

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Year:  1993        PMID: 8246980      PMCID: PMC364835          DOI: 10.1128/mcb.13.12.7636-7644.1993

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  40 in total

1.  DNA sequence variation associated with elevated fetal G gamma globin production.

Authors:  J G Gilman; T H Huisman
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2.  The British form of hereditary persistence of fetal hemoglobin results from a single base mutation adjacent to an S1 hypersensitive site 5' to the A gamma globin gene.

Authors:  V E Tate; W G Wood; D J Weatherall
Journal:  Blood       Date:  1986-12       Impact factor: 22.113

3.  A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobin.

Authors:  F S Collins; J E Metherall; M Yamakawa; J Pan; S M Weissman; B G Forget
Journal:  Nature       Date:  1985 Jan 24-30       Impact factor: 49.962

4.  G to A substitution in the distal CCAAT box of the A gamma-globin gene in Greek hereditary persistence of fetal haemoglobin.

Authors:  R Gelinas; B Endlich; C Pfeiffer; M Yagi; G Stamatoyannopoulos
Journal:  Nature       Date:  1985 Jan 24-30       Impact factor: 49.962

5.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.

Authors:  P Chomczynski; N Sacchi
Journal:  Anal Biochem       Date:  1987-04       Impact factor: 3.365

6.  The "beta-like-globin" gene domain in human erythroid cells.

Authors:  D Tuan; W Solomon; Q Li; I M London
Journal:  Proc Natl Acad Sci U S A       Date:  1985-10       Impact factor: 11.205

7.  Human gamma- to beta-globin gene switching using a mini construct in transgenic mice.

Authors:  J A Lloyd; J M Krakowsky; S C Crable; J B Lingrel
Journal:  Mol Cell Biol       Date:  1992-04       Impact factor: 4.272

8.  A distant gene deletion affects beta-globin gene function in an atypical gamma delta beta-thalassemia.

Authors:  P Curtin; M Pirastu; Y W Kan; J A Gobert-Jones; A D Stephens; H Lehmann
Journal:  J Clin Invest       Date:  1985-10       Impact factor: 14.808

9.  Beta-globin gene inactivation by DNA translocation in gamma beta-thalassaemia.

Authors:  D Kioussis; E Vanin; T deLange; R A Flavell; F G Grosveld
Journal:  Nature       Date:  1983 Dec 15-21       Impact factor: 49.962

10.  A molecular study of a family with Greek hereditary persistence of fetal hemoglobin and beta-thalassemia.

Authors:  B Giglioni; C Casini; R Mantovani; S Merli; P Comi; S Ottolenghi; G Saglio; C Camaschella; U Mazza
Journal:  EMBO J       Date:  1984-11       Impact factor: 11.598

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  40 in total

1.  Role of NF-Y in in vivo regulation of the gamma-globin gene.

Authors:  Z Duan; G Stamatoyannopoulos; Q Li
Journal:  Mol Cell Biol       Date:  2001-05       Impact factor: 4.272

2.  FKLF, a novel Krüppel-like factor that activates human embryonic and fetal beta-like globin genes.

Authors:  H Asano; X S Li; G Stamatoyannopoulos
Journal:  Mol Cell Biol       Date:  1999-05       Impact factor: 4.272

Review 3.  Control of globin gene expression during development and erythroid differentiation.

Authors:  George Stamatoyannopoulos
Journal:  Exp Hematol       Date:  2005-03       Impact factor: 3.084

4.  Genome architecture of the human beta-globin locus affects developmental regulation of gene expression.

Authors:  Susanna Harju; Patrick A Navas; George Stamatoyannopoulos; Kenneth R Peterson
Journal:  Mol Cell Biol       Date:  2005-10       Impact factor: 4.272

5.  Silencing of Agamma-globin gene expression during adult definitive erythropoiesis mediated by GATA-1-FOG-1-Mi2 complex binding at the -566 GATA site.

Authors:  Susanna Harju-Baker; Flávia C Costa; Halyna Fedosyuk; Renee Neades; Kenneth R Peterson
Journal:  Mol Cell Biol       Date:  2008-03-17       Impact factor: 4.272

6.  Silencing of human fetal globin expression is impaired in the absence of the adult beta-globin gene activator protein EKLF.

Authors:  A C Perkins; K M Gaensler; S H Orkin
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-29       Impact factor: 11.205

7.  A globin enhancer acts by increasing the proportion of erythrocytes expressing a linked transgene.

Authors:  H G Sutherland; D I Martin; E Whitelaw
Journal:  Mol Cell Biol       Date:  1997-03       Impact factor: 4.272

8.  Transient expression assay of Agamma-588 (A/G) mutations in the K562 cell line.

Authors:  Mohammad Hamid; Frouzandeh Mahjoubi; Mohammad Taghi Akbari; Hossein Khanahmad; Fatemeh Jamshidi; Sirous Zeinali; Morteza Karimipoor
Journal:  Iran Biomed J       Date:  2011

9.  Mutation of gene-proximal regulatory elements disrupts human epsilon-, gamma-, and beta-globin expression in yeast artificial chromosome transgenic mice.

Authors:  Q Liu; J Bungert; J D Engel
Journal:  Proc Natl Acad Sci U S A       Date:  1997-01-07       Impact factor: 11.205

10.  The A gamma-globin 3' element provides no unique function(s) for human beta-globin locus gene regulation.

Authors:  Q Liu; K Tanimoto; J Bungert; J D Engel
Journal:  Proc Natl Acad Sci U S A       Date:  1998-08-18       Impact factor: 11.205

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